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A tutorial on fine-tuning DeepSeek R1 for medical applications and integrating DSPy for reinforcement learning.

This tutorial will be structured for AI/ML engineers and medical professionals, covering:

  • Introduction: Overview of DeepSeek R1 and DSPy in medical AI.
  • Features & Benefits: Key advantages of this approach.
  • Warnings & Considerations: Potential risks and limitations.
  • Installation & Setup: Environment configuration and dependencies.
  • Dataset Preparation: Selecting and formatting medical datasets.
  • Fine-tuning DeepSeek R1: Using LoRA with Unsloth for efficient training.
  • Building DSPy Pipelines: Implementing modular medical reasoning components.
  • Advanced RL Algorithm Integration: Implementing GRPO and alternative RL methods.
  • Deployment: Local and cloud-based deployment strategies, including Docker setup.
  • Evaluation Metrics: Benchmarking model performance with medical accuracy metrics.

Introduction

DeepSeek R1 is an advanced open-source reasoning language model designed to rival proprietary systems like OpenAI’s “o1” model (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) It achieves strong chain-of-thought reasoning ability by training with reinforcement learning, enabling it to tackle complex problems step-by-step. Notably, DeepSeek R1 is free to use with no restrictions, making state-of-the-art AI accessible to everyone (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) This openness is especially valuable in medicine, where patient data privacy and model transparency are critical. AI engineers can fine-tune DeepSeek R1 on medical knowledge, and medical professionals can benefit from its clinical reasoning capabilities without sending data to third-party APIs.

DSPy (Declarative Self-Improving Python) is a framework from Stanford that helps build AI pipelines in a modular, declarative way (What Is DSPy? How It Works, Use Cases, and Resources | DataCamp) Instead of hand-crafting single prompts, developers use DSPy to define a sequence of modular reasoning steps (e.g. a symptom analysis module, a diagnosis module) and specify success metrics. DSPy “compiles” these into a pipeline and can automatically optimize prompts or even model weights to improve performance over time (What Is DSPy? How It Works, Use Cases, and Resources | DataCamp) (DSPy) In a medical AI context, DSPy allows chaining together tasks like information extraction, differential diagnosis, and explanation generation in a controlled manner. This yields a self-improving medical reasoning system: the pipeline can learn from feedback (for example, if a diagnosis was correct) and adjust to maximize accuracy.

Why use DeepSeek R1 with DSPy in healthcare? DeepSeek R1 provides the powerful language understanding and reasoning core, while DSPy adds structure and reinforcement learning integration to systematically improve the AI’s performance. Together, they enable creation of an AI doctor assistant that can reason through patient cases step-by-step and continuously learn from outcomes. In this tutorial, we will walk through the entire process: fine-tuning DeepSeek R1 for a medical domain, using LoRA for efficient training, building DSPy pipelines for medical reasoning, integrating advanced reinforcement learning algorithms (like GRPO and PPO) to refine the model, and finally deploying the solution in production. Both AI/ML engineers and medical professionals should find this guide accessible and informative – we’ll explain technical steps clearly and relate them to clinical utility. Let’s dive in.

Features & Benefits

DeepSeek R1 and DSPy offer several key advantages for medical AI applications:

  • State-of-the-Art Reasoning & Diagnostic Accuracy: DeepSeek R1 was designed to excel at complex reasoning tasks (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) allowing it to analyze clinical scenarios and form multi-step conclusions. It was trained with techniques that encourage long “chains of thought,” so it can articulate why it makes a certain diagnosis. A distilled 8B version of DeepSeek R1 has demonstrated similar reasoning capability as the full model (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) In practice, this means it can reach diagnoses or answers that align closely with medical experts. By fine-tuning on medical Q&A data, its accuracy on domain-specific questions (like identifying diseases from symptoms) can be very high. Users have noted DeepSeek R1’s performance is on par with top models like GPT-4 on many tasks (DeepSeek R1 on AWS: Making a 671B Model Run on Consumer ...) – a promising sign for clinical decision support. Moreover, DSPy’s chain-of-thought modules can further improve reliability by breaking problems into smaller steps, reducing reasoning errors. All of this translates to improved diagnostic accuracy when evaluated on medical benchmarks (e.g. higher exact-match correctness on test questions, which we will cover in Evaluation Metrics).

  • Efficiency and Cost-Effectiveness: Despite its power, DeepSeek R1 can be used efficiently thanks to quantization and Low-Rank Adaptation (LoRA) techniques. The model has innovative quantized formats (e.g. Unsloth’s 1.58-bit dynamic quantization) that dramatically reduce memory without significant accuracy loss (unsloth/DeepSeek-R1 - Hugging Face) Unsloth’s framework can load R1 in 4-bit mode for training and inference, enabling even a single GPU to handle the model (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) This efficiency is crucial in healthcare settings that may not have giant compute clusters. Fine-tuning with LoRA is also lightweight – only small adaptation matrices (with a rank like 16) are learned, which is 2-5× faster and uses ~70% less memory than standard fine-tuning (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) That means a hospital’s AI team can update the model with new medical data quickly and on a budget. Even inference is faster: R1 can generate answers at high throughput (reports of ~140 tokens/sec with optimized quantization) on affordable hardware In sum, you get cutting-edge performance without exorbitant compute costs.

  • Modularity and Maintainability: By using DSPy, the solution is organized into modular components that mirror logical clinical reasoning steps. For example, one module could extract key symptoms from a patient note, the next module (with a ChainOfThought prompt) reasons out possible diagnoses, and a final module provides the recommendation. This modular design makes the system easier to maintain and upgrade – you can improve or swap out one component (say, a new symptom extraction model) without rewriting the entire pipeline. It also improves transparency, since each module’s output can be inspected (e.g. the chain-of-thought reasoning can be printed for a doctor to review). DSPy’s declarative approach separates what the AI should do from how it’s prompted (What Is DSPy? How It Works, Use Cases, and Resources | DataCamp) (DSPy) This means the team can focus on defining medical tasks and quality metrics, while DSPy handles prompt engineering under the hood. Over time, the pipeline can even self-optimize its prompts or even fine-tune sub-components based on feedback, thanks to DSPy’s support for “learning” from evaluation metrics (DSPy) This results in a self-improving system that becomes more accurate and aligned with clinical needs as more cases run through it.

  • Compliance, Privacy, and Ethical Alignment: Both the model and pipeline can be deployed on-premises (or in a secure cloud), which is critical for patient data privacy. DeepSeek R1 being open-source allows hospitals to host it internally, ensuring no sensitive patient data leaves the secure environment – a key requirement for HIPAA compliance in the US. By contrast, relying on a third-party API could pose privacy risks. Additionally, because you have full control over the model, you can audit and adjust it for fairness and safety. If biases are identified (e.g. the model performs worse on underrepresented patient groups), engineers can retrain or recalibrate using specific datasets. This flexibility supports compliance with emerging AI regulations. Notably, regulatory bodies like the FDA have indicated that AI systems used for diagnosis or treatment will require oversight and rigorous validation (FDA lists top 10 artificial intelligence regulatory concerns) Using an open model facilitates this, since the exact model behavior can be examined and improved collaboratively (no black-box model). In short, DeepSeek R1 + DSPy can be made to align with medical standards for accuracy, accountability, and transparency. Proper documentation of the model’s training data and behavior can help in future regulatory approval processes if the tool is used clinically.

These features make DeepSeek R1 and DSPy a powerful combo: you get a highly accurate, efficient AI doctor assistant that you can trust and verify. Next, we’ll address important warnings and ethical considerations to keep in mind before deploying such a system in healthcare.

Warnings & Considerations

Deploying Large Language Models in healthcare comes with significant risks and ethical considerations. It’s critical to acknowledge these and implement safeguards:

  • Potential for Incorrect or Fabricated Outputs (Hallucinations): LLMs like DeepSeek R1 do not truly “understand” medicine – they generate outputs based on patterns in training data. This means they can sometimes produce confident-sounding but incorrect answers. For example, the model might hallucinate a nonexistent drug or misstate a dosage. In a medical context, such errors can cause harm if not caught. All outputs, especially diagnoses or treatment suggestions, must be verified by a qualified medical professional. One should never blindly trust the AI. Building in checks (e.g. have the model cite sources or cross-verify symptoms) can mitigate this, but human oversight is paramount. Additionally, structured reasoning via DSPy can help catch errors (since intermediate reasoning steps can be reviewed), but it’s not foolproof. Always use the model as an assistant, not an autonomous decision-maker.

  • Bias in Training Data Leading to Bias in Outputs: If the model’s training data (even the specialized fine-tuning data) contains biases, the model may reflect or even amplify those biases. For instance, if certain demographics were underrepresented or if existing biases in care (like misdiagnosis rates in certain groups) are present in the data, the model could perpetuate them. Research has highlighted that even with unbiased data, algorithmic bias can creep in via the model’s design, potentially leading to clinical errors with serious consequences ( Ethical Considerations of Using ChatGPT in Health Care - PMC ) It’s essential to evaluate the model’s performance across diverse patient groups and mitigate biases. This might involve adding training examples for underrepresented cases or adjusting the output with post-processing rules. Ethically, the model should promote fair and equitable care. We must be cautious that recommendations don’t systematically favor or disadvantage any group.

  • Ethical and Legal Accountability: The use of an AI model for clinical decision support raises questions of liability. If the AI gives a harmful recommendation and a patient is hurt, who is responsible – the doctor, the hospital, or the developers of the model? Currently, this is a gray area. Legal and regulatory frameworks are still catching up to AI in medicine ( Ethical Considerations of Using ChatGPT in Health Care - PMC ) For now, clinicians should treat the AI’s advice as they would a less-experienced colleague’s suggestion: consider it, but ultimately the licensed professional is responsible for decisions. It’s wise to keep thorough logs of the model’s suggestions and the rationale for either following or disregarding them. This transparency can help in auditing and explaining decisions. On the regulatory side, note that as of late 2024, the FDA has not authorized any LLM as a medical device, but it has indicated that many such applications will fall under its oversight (FDA lists top 10 artificial intelligence regulatory concerns) So, any deployment in a clinical setting should be done in a research or pilot capacity with proper patient consent and institutional review, until formal approval is achieved.

  • Patient Privacy and Data Security: Medical data used for fine-tuning or prompting the model is highly sensitive. It’s imperative to follow privacy laws (like HIPAA) and institutional policies. De-identify patient data whenever possible during training – remove names, IDs, and other direct identifiers. Even so, be mindful that a large model might memorize specifics if overfit, so use techniques to prevent that (don’t fine-tune on very small sets of unique patient data verbatim, for example). When deploying, ensure the system is secure: if it’s a cloud deployment, use HIPAA-compliant services, encryption for data in transit and at rest, and strict access controls. Also, avoid sending any patient queries to external services during operation. One reason to prefer DeepSeek R1 (self-hosted) over a third-party model is to maintain full control over patient data – no data needs to leave your environment, reducing risk of breaches.

  • Model Limitations and Continuous Monitoring: No matter how well fine-tuned, an LLM will have limitations. It might not be up-to-date with the latest medical research (unless you regularly retrain it on new literature). It could misinterpret ambiguous questions or fail to grasp visual data (if the case requires imaging analysis, for instance, an LLM alone won’t suffice). Be aware of what the model can and cannot do. For any automated system in healthcare, you should establish a process for continuous monitoring and improvement. This includes gathering feedback from the clinicians using it: Are the AI’s suggestions actually helpful? Did it ever give a dangerous answer? Regularly review a sample of outputs for quality and safety. Many experts recommend a human-in-the-loop approach: use AI to draft or suggest, but always have a human verify. Also, maintain a reporting mechanism so if a provider or patient spots an incorrect or harmful recommendation, it’s logged and can inform future model adjustments. Ongoing validation is crucial – as one publication noted, ensuring accuracy and reliability of AI outputs requires rigorous validation and updates based on clinical practice ( Ethical Considerations of Using ChatGPT in Health Care - PMC )

By keeping these considerations in mind, we can minimize risks while leveraging the powerful capabilities of DeepSeek R1. Next, we will proceed with the hands-on aspects: setting up the environment for fine-tuning and pipeline development.

Installation & Setup

Fine-tuning a large model like DeepSeek R1 and using DSPy involves setting up a suitable environment with the right hardware and software. Below is a step-by-step guide to get started:

1. Prepare the Hardware and OS:
You’ll need access to a machine with a GPU (or multiple GPUs) if you plan on fine-tuning the model in a reasonable time. DeepSeek R1’s distilled 8B variant can be fine-tuned on a single modern GPU (e.g. 24 GB VRAM) especially with 4-bit loading, but the full R1 (hundreds of billions of parameters) would require a multi-GPU server (and is beyond scope for most). For this tutorial, assume we use the 8B model or similar. A Linux environment (Ubuntu 20.04+ or equivalent) is recommended for compatibility with machine learning libraries. Ensure you have the latest NVIDIA drivers and CUDA toolkit installed if using an NVIDIA GPU. If you don’t have local hardware, consider using a cloud GPU instance or a platform like Kaggle Notebooks or Google Colab, which provide free GPU runtimes (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) (the DataCamp example uses Kaggle’s free GPU).

2. Set Up Python Environment:
Install Python 3.9+ (3.10 recommended) via Anaconda or pyenv for an isolated environment. It’s wise to use a virtual environment to avoid dependency conflicts. For example:

conda create -n deepseek_env python=3.10
conda activate deepseek_env

Alternatively, python -m venv venv can create a virtualenv. Once activated, upgrade pip: pip install --upgrade pip.

3. Install Required Libraries:
We will use several libraries: Unsloth (for efficient model loading and fine-tuning), Transformers (Hugging Face library underlying the model), Datasets (for data handling), PEFT/LoRA (built into Unsloth’s methods), TRL (Hugging Face’s reinforcement learning library), and DSPy. Install these via pip:

pip install unsloth transformers datasets accelerate trl
pip install dspy-ai

Let’s break that down: unsloth is an open-source toolkit that will make fine-tuning faster and more memory-efficient (achieving 2× speed-up in LLM fine-tuning) (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) The second line installs DSPy; the package name is dspy-ai on PyPI (What Is DSPy? How It Works, Use Cases, and Resources | DataCamp) The trl library will let us apply PPO or other RL algorithms later. You should also install PyTorch if it’s not already (pip installing transformers usually brings torch as a dependency, but if not, do pip install torch appropriate for your CUDA version). Additionally, if you plan to use Weights & Biases (wandb) for experiment tracking as the DataCamp tutorial did, install it and login (pip install wandb, then wandb login). That step is optional.

4. (Optional) Authenticate Hugging Face for model access:
The DeepSeek R1 weights (especially the large ones) might be gated behind a user agreement on Hugging Face. If so, you’ll need to accept the terms on the Hugging Face website and use an API token to download. You can login via Hugging Face CLI:

from huggingface_hub import login
login("your-hf-api-token")

This will allow the from_pretrained calls to download the model. If you’re using a hosted runtime (Colab/Kaggle), store your token securely (Kaggle has a Secrets feature (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) .

5. Verify Installation:
After installing, launch a Python interpreter and try to import the libraries to ensure they installed correctly:

import torch; import unsloth; import dsp  # dsp is the import name for DSPy

Also, check that PyTorch recognizes your GPU:

torch.cuda.is_available()

This should return True if GPU is accessible. If using CPU only (not recommended for fine-tuning due to slowness), ensure enough RAM and consider smaller batch sizes.

With the environment ready, we can proceed to prepare our dataset for fine-tuning.

Dataset Preparation

A crucial step in fine-tuning is preparing a specialized medical dataset that will teach DeepSeek R1 the domain-specific knowledge or task (e.g. answering medical questions or assisting in diagnoses). Here’s how to approach dataset selection and preparation:

1. Choose a Relevant Dataset: Decide what task you want to fine-tune for. Some examples: a Medical Q&A dataset (question and detailed answer pairs, possibly with chain-of-thought), a clinical dialogue dataset (doctor-patient conversations), or a diagnosis dataset (case descriptions with the correct diagnosis). For this tutorial, we use the Medical Chain-of-Thought dataset released on Hugging Face, which contains medical exam questions and answers with step-by-step reasoning. In fact, the DataCamp guide fine-tuned on a “Medical COT” dataset curated by FreedomIntelligence (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) You can load this or any Hugging Face dataset easily with the datasets library. For instance:

from datasets import load_dataset

dataset = load_dataset("FreedomIntelligence/medical-o1-reasoning-SFT", "en", 
                       split="train")

This particular dataset (in English, split 'train') is a set of medical questions along with chain-of-thought and answer, designed to fine-tune models like DeepSeek to provide reasoning (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) If you have your own data (say, a collection of patient cases and outcomes), you’ll need to format it into a similar structure (more on formatting below). Always ensure you have permission to use the data – if it’s real patient data, remove personal identifiers and get necessary approvals.

2. Understand the Format and Create a Prompt Template: Language models are typically fine-tuned on text where each example is a prompt-response pair. We need to format the medical data into a prompt that the model will see, and the expected output. For example, a common format is an instruction followed by an input, then the model’s response. In our case, the “instruction” might be something like: “You are a medical assistant. Given the following patient case, provide a step-by-step reasoning and the final diagnosis.” The “input” would be the case details or question. And the response is what we want the model to learn to generate (the chain of thought + answer). In the DataCamp example, they defined a prompt template guiding the model to think step-by-step (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) You can do similarly. For instance:

prompt_template = """Below is an instruction that describes a task, paired with an input that provides further context. 
Write a response that completes the request.

Instruction: Provide a medical diagnosis with reasoning.
Input: {case_description}
Thought:<think> Let's reason step by step. {chain_of_thought}
Diagnosis: {answer}"""

Here we use placeholders {case_description}, {chain_of_thought}, {answer} that we will fill in from our dataset. If your dataset already has a combined field (some datasets might have the full prompt ready), you might not need to do this manually. In our code, after loading the dataset, we likely will .map() a function over it to join the question, chain-of-thought, and answer into one text field that the model will be trained on. The Kaggle code did something similar with a formatting_prompts_func mapping (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp)

3. Preprocess and Clean the Data:
Perform any necessary cleaning. Remove or correct obviously wrong data points that might confuse training. Ensure that all text is in a consistent encoding (UTF-8). If the dataset is large, you might sample or filter it for quality – sometimes a smaller high-quality dataset yields better results than a noisy large one. For example, if using a public dataset, you might drop examples that have incomplete information. Also consider splitting a portion (say 10-20%) as a validation set to monitor training performance and avoid overfitting. The Hugging Face load_dataset can often provide predefined train/val splits, or you can use dataset.train_test_split() to carve out a validation set.

4. Tokenization Considerations:
DeepSeek R1 (being based on Llama architecture as indicated by “Llama-8B” in the distilled model (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) will have a specific tokenizer. When we load the model, we’ll get its tokenizer. It’s important the dataset text is compatible with this tokenizer (which it will be, if we use the same model’s vocabulary). If you have very domain-specific terms (like rare disease names, chemical compounds), verify that the tokenizer can handle them (it likely will break them into subword tokens – that’s fine). You don’t need to tokenize manually; the training pipeline will do it, but be mindful of the sequence length. Clinical case descriptions plus chain-of-thought can be long. DeepSeek R1 supports up to 2048 tokens context by default (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) If your combined prompt + answer exceeds that, you may need to truncate or shorten some examples (or use only part of the chain-of-thought during training if it’s extremely long). In general, try to keep each training example within the model’s max context length.

5. Finalize the Training Dataset Object:
After formatting, you should have a dataset (for example a HuggingFace Dataset) where each entry has a field like “text” containing the full prompt+response sequence you want the model to learn. For instance, one “text” might look like:

Instruction: Provide a medical diagnosis with reasoning. Input: 45-year-old male with chest pain... ... Diagnosis: Myocardial infarction (just as an illustrative example).

We will feed this dataset into the training loop. If using SFTTrainer or Hugging Face Trainer, typically you provide the dataset and specify which column is the text to use. In our case, we’ll use the “text” field as input (and the trainer will handle internally that the model is supposed to predict the next tokens, i.e., effectively learning to output the answer when given the prompt part).

Before training, double-check: Are there any obvious privacy issues in the data? Is everything properly anonymized? Are the outputs something you want the model to mimic? (For example, if the answers contain phrases like “As an AI, I can’t do X,” you might want to remove those, since our fine-tuned model should act as a helpful medical AI, not referencing itself.) A clean, well-structured dataset will set the foundation for a successful fine-tuning.

Now that our data is ready, let’s move on to the fine-tuning process itself, leveraging LoRA and Unsloth for efficiency.

Fine-tuning DeepSeek R1 with LoRA (using Unsloth)

Fine-tuning DeepSeek R1 on your medical dataset allows the model to adapt its knowledge to the specific style and content of your task. We will use LoRA (Low-Rank Adaptation) to do this efficiently, updating only small adapter weights instead of the full model. Unsloth’s API provides convenient helpers to apply LoRA to the model. Here’s the step-by-step:

1. Load the Pretrained Model in 4-bit Mode:
Using Unsloth, we can load the model with 4-bit quantization to save memory. We’ll load the DeepSeek-R1-Distill-Llama-8B model (8B parameter version distilled from the full R1, as mentioned) from Hugging Face (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) For example:

from unsloth import FastLanguageModel

model_name = "unsloth/DeepSeek-R1-Distill-Llama-8B"
max_seq_length = 2048  # max context
model, tokenizer = FastLanguageModel.from_pretrained(
    model_name,
    max_seq_length=max_seq_length,
    load_in_4bit=True,   # use 4-bit quantization
    token=YOUR_HF_TOKEN  # if needed for authentication
)

This uses Unsloth’s FastLanguageModel class to handle loading. We pass load_in_4bit=True to dramatically reduce memory usage (4-bit quantization). The model will be loaded on the GPU in half precision by default (FP16 or BF16). The tokenizer will be a LLaMA-architecture tokenizer ready to encode our inputs. Ensure max_seq_length is at least as large as the longest sequence in our dataset (2048 tokens as set, which is the model’s max). If you get an out-of-memory error at this step, you might need to use an even more aggressive quantization (like 1.58-bit quant, but that requires the special weights from Unsloth’s dynamic quantization blog (unsloth/DeepSeek-R1 - Hugging Face) or use CPU offloading via accelerate. But typically 4-bit on 8B model is fine on a 16GB GPU.

2. Prepare LoRA Adapter Configuration:
LoRA works by injecting trainable low-rank matrices into certain layers of the model. We need to specify which layers to target (e.g., W_q, W_k, W_v in attention, etc.). The DataCamp tutorial targeted several transformer sub-modules: query, key, value projections, output projection, and the feedforward layers’ projections (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) We can use a similar list. We also choose the LoRA hyperparameters like rank (r), alpha scaling, and dropout. For instance:

target_modules = ["q_proj", "k_proj", "v_proj", "o_proj", "gate_proj", "up_proj", "down_proj"]  # layers to apply LoRA
lora_rank = 16
model = FastLanguageModel.get_peft_model(
    model,
    r=lora_rank,
    target_modules=target_modules,
    lora_alpha=16,
    lora_dropout=0.0,
    bias="none",
    use_gradient_checkpointing="unsloth"  # enable gradient checkpointing for memory saving ([Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp](https://www.datacamp.com/tutorial/fine-tuning-deepseek-r1-reasoning-model#:~:text=lora_alpha%3D16%2C%20lora_dropout%3D0%2C%20bias%3D,long%20context%20random_state%3D3407%2C%20use_rslora%3DFalse%2C%20loftq_config%3DNone)) )

Here get_peft_model is a helper that wraps the model with LoRA using PEFT under the hood. We pass use_gradient_checkpointing="unsloth" which is a neat trick: Unsloth can automatically checkpoint long sequences to save memory during backpropagation (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) This is very useful for 2048-token sequences. We set r=16 and lora_alpha=16 which are common choices – effectively the LoRA weights will have an internal scaling factor so that the update magnitude is appropriate (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) bias="none" means we won’t add any trainable bias vectors (focusing only on the low-rank matrices). With dropout 0, we are not randomly dropping adapter updates (you could add dropout if you find overfitting, but usually 0 is fine for LoRA). Now our model is a PEFT model with additional parameters (initially zeroed out) that we will train, while the original pre-trained weights remain fixed. This greatly reduces the number of parameters we’ll update (and store).

3. Set Training Arguments:
We need to specify how we will fine-tune (learning rate, batch size, number of steps, etc.). We’ll use Hugging Face’s Trainer API or the TRL’s SFTTrainer for convenience. Let’s use SFTTrainer from TRL as in the DataCamp example, which is basically a Trainer specialized for supervised fine-tuning (SFT):

from trl import SFTTrainer
from transformers import TrainingArguments

training_args = TrainingArguments(
    output_dir="outputs",
    max_steps=100,  # or specify num_train_epochs, but max_steps is fine for demo
    per_device_train_batch_size=2,
    gradient_accumulation_steps=4,
    learning_rate=2e-4,
    warmup_steps=5,
    logging_steps=10,
    bf16= True,  # if your GPU supports BF16 (e.g., A100); else use fp16
    fp16= True,  # for mixed precision training
    seed=3407,
    optim="adamw_bnb_8bit",  # use 8-bit Adam optimizer for less memory ([Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp](https://www.datacamp.com/tutorial/fine-tuning-deepseek-r1-reasoning-model#:~:text=args%3DTrainingArguments%28%20per_device_train_batch_size%3D2%2C%20gradient_accumulation_steps%3D4%2C%20,4%2C%20fp16%3Dnot%20is_bfloat16_supported%28%29%2C%20bf16%3Dis_bfloat16_supported))     weight_decay=0.01
)
trainer = SFTTrainer(
    model=model,
    tokenizer=tokenizer,
    train_dataset=dataset,               # our prepared Dataset object
    dataset_text_field="text",           # field name in dataset to use
    max_seq_length=max_seq_length,       # 2048
    args=training_args
)

A few things to note: We use a small per_device_train_batch_size (2 here) because large language models consume a lot of memory per sample, especially with long sequences. Gradient accumulation of 4 means effectively batch size of 2×4=8 in terms of updates, which is okay. max_steps=100 is just for demonstration – in practice, you might train for an epoch or two over the dataset. For a larger dataset, you’d use num_train_epochs instead (and potentially many more steps; the DataCamp tutorial did only 60 steps on a sample for demo (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) but a full fine-tune might be thousands of steps). The learning rate 2e-4 is relatively high for fine-tuning; monitor loss and lower it if the model starts diverging (you could start around 1e-4 as well). We include a few warmup steps to gently ramp up learning rate at the start (avoids instability). We enable 8-bit Adam (adamw_bnb_8bit) via bitsandbytes to save memory (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) The seed is set for reproducibility. Also, note we set both bf16 and fp16. Here, we attempted BF16 first (if the hardware supports it; if not, is_bfloat16_supported() would be False and we’d fallback to FP16 as shown in the DataCamp code (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) . BF16 can be slightly more stable on some GPUs like A100. If using an older GPU, stick to FP16.

4. Begin Training:
Now we can launch the fine-tuning process:

trainer.train()

This will loop over the dataset and update the LoRA weights. Thanks to our settings, this process is quite fast. In a test run, fine-tuning on a subset of ~500 examples took under an hour (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) As it trains, you should see the loss decreasing in the logs every few steps, indicating the model is adapting. Ideally, also monitor an evaluation loss if you set aside a validation set (you can pass eval_dataset to SFTTrainer and call trainer.evaluate() periodically). Since we’re using LoRA, the original model weights remain unchanged on disk; the learned LoRA adapters are in memory and will be saved in the output_dir as a small file (possibly a .bin or .pt file only tens of MB).

5. Save and/or Merge LoRA Weights:
After training, you will want to save the fine-tuned model. The Trainer should save the final checkpoint in output_dir. This usually includes the adapter weights and a config. To use the model for inference, you have two choices:

  • Load the base model again and apply the LoRA weights dynamically (requires your code to do the get_peft_model step and then load the saved LoRA state dict).
  • Or merge the LoRA weights into the base model to create a standalone model. Merging will apply the low-rank updates to the original weights permanently. Unsloth provides utilities to merge LoRA and even to export to efficient runtimes like GGUF (unsloth/DeepSeek-R1-Distill-Llama-8B · Hugging Face) For example, you could use Unsloth or PEFT’s functions to merge and then save a full model. Merging is convenient for deployment because you then just have one model file. However, if you plan to keep fine-tuning further or toggle the adapter on/off, keeping them separate is fine.

6. Best Practices Recap: Always verify the model’s outputs on some example queries after fine-tuning. Ask it a few questions from the training data and a few that it hasn’t seen. It should follow the chain-of-thought format and give reasonable answers. If it’s just regurgitating training answers without adaptation, maybe it was under-trained. If it’s giving nonsense or losing general ability, maybe it was over-trained (or catastrophic forgetting – which is less likely with LoRA since base weights are intact). You can adjust hyperparameters accordingly (e.g., train longer if underfit, or use a lower learning rate or more data if overfit). Also note that DeepSeek R1 was originally trained via RL; our supervised fine-tune is aligning it to medical data, but we might later fine-tune with RL too for final polish – that’s where DSPy and advanced RL (next sections) come in.

At this stage, you have a DeepSeek R1 model adapted to your medical task. Next, we will see how to utilize DSPy to create a structured pipeline around this model, allowing more complex reasoning and integration of multiple steps (and eventually, feedback-based improvement).

Building DSPy Pipelines for Medical Reasoning

Now that we have a fine-tuned medical model, the next step is to build a pipeline that uses the model in a controlled, multi-step reasoning process. This is where DSPy shines. Instead of prompting the model with one big instruction, we can break the task into modules – for example: summarizing patient information, generating differential diagnoses, asking follow-up questions, and then finalizing a diagnosis. Each module can be implemented with DSPy, and together they form a pipeline that can be optimized and maintained easily.

1. Configure DSPy to Use the Fine-Tuned Model:
DSPy by default can work with OpenAI API or other backends, but we want it to use our local DeepSeek R1 model. We have a few options: we could wrap our model in an interface that DSPy accepts (DSPy has something called HFClient or HFClientTGI for Hugging Face models (HFClientTGI - DSPy) . One straightforward approach is to run a local text-generation server (like Hugging Face’s text-generation-inference or FastAPI) for our model and point DSPy to it. For simplicity, let’s assume we can call our model via a Python function. DSPy’s modules will use whatever the current default language model is for generating text. In the latest DSPy, you might set something like:

import dsp
dsp.settings.configure_default_backend(model=tokenizer, tokenizer=tokenizer)  # pseudo-code

(The exact API for setting a custom model may depend on DSPy version, so consult the DSPy docs for “local models”.)

Alternatively, if integration is complex, one can use DSPy with OpenAI during development and replace calls with the local model for deployment to ensure consistency. But assuming we have it set, we proceed to define modules.

2. Define Modular Components:
DSPy modules are defined by signatures. For example, dspy.Predict('symptoms -> diagnosis') means a module that takes “symptoms” as input and outputs a “diagnosis”. We can also use dspy.ChainOfThought to automatically include a reasoning step. Let’s create a simple pipeline with two modules for illustration: one module will consolidate the patient info, and another will produce reasoning + diagnosis.

import dsp

# Module 1: Summarize or preprocess patient info (could be identity in this simple case)
summarize = dsp.Predict('raw_text -> summary')
# Module 2: Perform chain-of-thought reasoning to get a diagnosis
diagnose = dsp.ChainOfThought('summary -> reasoning, diagnosis')

Here, summarize is a trivial placeholder (it might just pass through or shorten text). The interesting part is diagnose, which we declared with a signature indicating input “summary” and outputs “reasoning” and “diagnosis”. The ChainOfThought module will automatically prompt the model to generate a hidden reasoning and a final answer (Modules - DSPy) (Modules - DSPy) Essentially, DSPy knows to format the prompt so that the model’s output includes a reasoning step followed by the answer, separated internally, and it returns an object where we can access response.reasoning and response.diagnosis.

Let’s use these modules in a pipeline:

# Example usage:
patient_case = "45-year-old male with sudden chest pain radiating to left arm and jaw, sweating."
res1 = summarize(raw_text=patient_case)
print("Summary:", res1.summary)

res2 = diagnose(summary=res1.summary)
print("Chain-of-Thought:", res2.reasoning)
print("Diagnosis:", res2.diagnosis)

In this snippet, the diagnose module will prompt the model behind the scenes. Under the hood, DSPy might create a prompt like: “Given the summary, let's reason step by step: ... [model generates reasoning] ... Therefore, the diagnosis is ... [model generates diagnosis]”. The output is captured in res2. We can inspect the reasoning and final diagnosis separately. For example, it might output:

Chain-of-Thought: The patient’s symptoms (chest pain radiating to arm and jaw, diaphoresis) strongly suggest an acute coronary syndrome, likely a myocardial infarction.
Diagnosis: Myocardial infarction (heart attack)

This separation is extremely useful in medical settings – you can choose to show the clinician the reasoning for transparency.

3. Composing Pipelines with Multiple Modules:
The above was a linear two-step pipeline. DSPy allows more complex composition as well. You could, for instance, have a module that checks if the initial summary is unclear and asks a follow-up question (and another module that “answers” using the model). Or integrate retrieval: e.g., use a dspy.Search module to retrieve relevant medical literature for rare diseases, and feed that into the reasoning module. The possibilities are endless, but they all follow the pattern of declarative modules. Another example:

# Module 3: Retrieve similar cases from a knowledge base (hypothetical)
retrieve = dsp.Predict('summary -> supporting_info')
# We could imagine supporting_info includes some text from guidelines or prior cases.

Then we could expand the diagnose signature to use that:

diagnose = dsp.ChainOfThought('summary, supporting_info -> reasoning, diagnosis')

And call:

info = retrieve(summary=res1.summary)
res2 = diagnose(summary=res1.summary, supporting_info=info.supporting_info)

This way, the model gets to see external info (like “supporting_info”) and incorporate it into reasoning. This is analogous to Retrieval-Augmented Generation (RAG), but done within DSPy’s framework.

4. DSPy Pipeline Execution and Iteration:
You can create a function or class to encapsulate the whole pipeline. For example:

def diagnose_patient(case_text):
    res1 = summarize(raw_text=case_text)
    res2 = diagnose(summary=res1.summary)
    return res2  # contains reasoning and diagnosis

Now diagnose_patient can be called with any new case text to get a model-generated reasoning and diagnosis. This could be hooked into a web app or CLI for clinicians to use.

One of DSPy’s strengths is that it allows you to optimize these modules together. If you have an evaluation metric (say, did the diagnosis match the known correct answer in a test set), DSPy can use that to adjust prompts or even fine-tune weights in a multi-module pipeline (DSPy) (DSPy) For instance, DSPy has optimizers like dspy.BootstrapRS (to synthesize better few-shot examples for prompts) or dspy.MIPROv2 (to reword prompts) and even dspy.BootstrapFinetune (to finetune the model on failures) (DSPy) Advanced users can leverage these to gradually improve the pipeline’s performance on a validation set. As a simple example, if the model often misses a certain step in reasoning, an optimizer could detect that via the metric and adjust the chain-of-thought prompt.

For our tutorial scope, the main takeaway is that DSPy allows you to structure the interaction with the model in a way that mirrors medical reasoning steps. This structure will be helpful when we integrate reinforcement learning signals, as we can pinpoint where mistakes happen (e.g., maybe the model reasons well but picks the wrong final answer – we could then focus an RL reward on the final answer correctness).

In the next section, we’ll discuss how to integrate advanced reinforcement learning algorithms (like GRPO, PPO, TRPO) to further enhance the model’s performance, using either DSPy’s optimization or direct RL fine-tuning techniques.

Advanced Reinforcement Learning Integration (GRPO, PPO, TRPO)

Fine-tuning with supervised data is powerful, but reinforcement learning (RL) can further refine the model’s behavior by directly optimizing for outcomes we care about. In the context of DeepSeek R1, RL was a core part of its training – in fact, Group Relative Policy Optimization (GRPO) was introduced for training the original R1 from scratch (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) We’ll cover how GRPO differs from other RL methods and how to integrate such algorithms into our pipeline. We’ll also discuss using more established methods like PPO and TRPO for our medical AI.

1. Generative Reward-Penalty Optimization (GRPO):
GRPO is a variant of the popular Proximal Policy Optimization (PPO) algorithm, tailored for language model training. The key difference in GRPO is that it does not use a separate value (critic) model to baseline rewards. Instead, it groups multiple generated outputs and uses their relative scores as the baseline (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) In the DeepSeek training, the researchers would generate a group of responses to a prompt, give each a reward (based on criteria like correctness and format), and then rank them, using the group’s own score distribution to normalize the advantages. This simplification removes the need to train a value network to predict reward, which can make RL training more stable and easier to scale for LLMs (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) In their setup, rewards were given for accuracy (did the answer solve the problem correctly?) and for adhering to a chain-of-thought format (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) You could apply the same concept in medical fine-tuning: define a reward function that, for example, gives +1 if the model’s diagnosis is correct and 0 if not, and maybe a smaller reward for including a reasoning path. Then have the model generate a few different answers via sampling and update it to increase the probability of the better-scoring answers (and decrease probability of worse ones). GRPO essentially does “PPO without a critic, using group relative rewards” (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean)

How to implement GRPO in practice? As of now, GRPO is not as readily available in libraries as PPO, but it’s conceptually simple to implement on top of a PPO framework by altering the advantage calculation. The good news: if you don’t want to code it from scratch, you might approximate GRPO by PPO with a very lightweight or no value network. The Hugging Face TRL library focuses on PPO, but one could modify it. There is also a reference to a HuggingFace trainer for GRPO (GRPO Trainer - Hugging Face) indicating an implementation is available. For this tutorial’s purposes, you could proceed with PPO (which we’ll discuss next) and know that GRPO would be a specialized improvement if needed. In summary, GRPO is useful when you have well-defined reward signals (like accuracy) and want a simpler training loop. It was crucial in enabling DeepSeek R1 to learn reasoning solely from a reward signal (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean)

2. Proximal Policy Optimization (PPO):
PPO is a popular RL algorithm that has been used in training language models from human feedback (RLHF) and other settings. It works by taking the current policy (the model) and gently nudging it to improve on a given reward function, while not straying too far from the original distribution (this is enforced by a clipping mechanism on probability ratios). In our scenario, we can use PPO to fine-tune the model’s responses to maximize a reward, such as correctness of the diagnosis or satisfaction of the doctor using it. For example, if we have a dataset of case -> correct diagnosis, we can define the reward as +1 for giving the correct diagnosis and maybe -1 for a wrong one (or a continuous score if partial credit). We then have the model generate a diagnosis for each case, compute the reward, and use PPO to update the model. We would iterate this process, similar to how one would do RLHF (where a "reward model" gives a score to the response).

The Hugging Face TRL library makes it easier to apply PPO to language models (PPO Trainer - Hugging Face) You would typically:

  • Initialize a PPOTrainer with the model, a reference model (usually a copy of the original to measure relative change), the tokenizer, and the training dataset of prompts.
  • Define a reward_fn that given a prompt and generated response, returns a reward score. (This could be rule-based or learned; for instance, you could train a separate classifier that judges if the diagnosis is correct based on the input and expected output, or just compare to ground truth in a dataset).
  • Then in a loop, have the PPOTrainer generate responses for prompts and apply the reward function, and call ppo_trainer.step to update.

Pseudocode with TRL:

from trl import PPOTrainer, PPOConfig

# Suppose we have a list of prompts (cases) and a function get_reward(prompt, response)
ppo_config = PPOConfig(batch_size=1, forward_batch_size=1, log_with=None)  # simplified config
ppo_trainer = PPOTrainer(config=ppo_config, model=model, ref_model=model, tokenizer=tokenizer)

for prompt in prompts:
    # Generate response
    response = model.generate(tokenizer.encode(prompt, return_tensors='pt').to(model.device))
    response_text = tokenizer.decode(response[0], skip_special_tokens=True)
    reward = get_reward(prompt, response_text)
    # Optimize model on this single example
    ppo_trainer.step([prompt], [response_text], [reward])

In practice, you’d do this in batches and for many epochs over the data. Note: TRL expects the ref_model which is a stable copy of the model (pre-RL) to compute KL-divergence penalty, ensuring the new model doesn’t drift too far from original (this is part of PPO’s loss along with the reward). The above is just illustrative; a real implementation needs careful handling of tokenization and multiple epochs. But conceptually, PPO fine-tuning allows the model to directly optimize for outcomes. If the outcome is something like “correct diagnosis”, PPO can improve that metric potentially beyond what supervised learning did, at the cost of possibly making the model’s outputs more focused and maybe less diverse (hence the need for the KL penalty).

For our pipeline using DSPy, one strategy is to use the pipeline outputs to define rewards. For example, reward = 1 if diagnosis output equals the ground truth for a case AND maybe subtract a small penalty if the reasoning (reasoning output) contains a known error or contradiction. Then you could update the model with PPO. If using DSPy’s own optimizers, an alternative is dspy.BootstrapFinetune which effectively does a form of fine-tuning on failures (this might use supervised signals rather than true RL). But since the question explicitly mentions PPO and TRPO, we focus on those.

3. Trust Region Policy Optimization (TRPO):
TRPO is an older cousin of PPO. It also aims to keep updates small to not break the policy, but it does so with a more complex conjugate-gradient approach and an explicit KL divergence constraint instead of PPO’s clipping. TRPO updates the policy in a way that guarantees (theoretically) not too large a change, which can stabilize training. However, TRPO is more complex to implement and has largely been supplanted by PPO for practical reasons (PPO is simpler and tends to work nearly as well). If one wanted to try TRPO on a language model, they’d need an implementation that can handle the large parameter space. Few off-the-shelf tools do TRPO for transformers currently. You might find TRPO in general RL libraries like Stable-Baselines3, but integrating that with a transformer would be non-trivial.

That said, the mention of TRPO suggests considering it as an alternative algorithm. For completeness: TRPO would involve computing the policy gradient and then projecting it into a trust region. In an LLM context, it could potentially be even more stable than PPO (preventing overshooting in updates), but might be slower. Unless you have a specific need or existing code for TRPO, PPO tends to be the go-to. If one were experimenting academically, they might implement TRPO to see if it yields any gains for LLM fine-tuning on, say, a sparse reward task.

4. Integrating RL into the DSPy Pipeline:
Where do we apply RL in our pipeline? Potentially at multiple points: you could apply a reward to the final diagnosis only, or to the whole chain-of-thought. For example, if the reasoning is important, you might structure the reward to encourage true reasoning. Perhaps you have some cases with explanations and you reward the model if its reasoning contains certain key points (this is harder to automate). A simpler approach is to focus on the final answer: reward = +1 if correct diagnosis, 0 if not. This signal can then propagate through the model because the chain-of-thought module affects the final answer generation. Over many cases, the model will statistically adjust.

Using DSPy, one can treat the entire pipeline as a black box to optimize. In fact, DSPy’s philosophy is to define a metric on the final output and let the optimizer tune everything to improve that metric (DSPy) For instance, define metric = accuracy of diagnosis on a validation set. Then one could use DSPy’s weight tuning optimizer (which likely uses something akin to PPO under the hood) to adjust the model’s weights (or prompt) to improve that. This is conceptually similar to what we described with PPOTrainer, but abstracted. If doing it manually with TRL, you might bypass DSPy during the RL fine-tuning phase: just sample outputs from your model for each case in a training set, compute rewards, and update the model (which is the core of PPO/GRPO training). After a number of RL steps (say a few epochs through your cases), you would have an updated model that hopefully scores higher on your metric.

Summary of RL Integration: Reinforcement learning can significantly boost the model’s performance on objectives that are hard to fully capture with supervised data. In healthcare, this could mean optimizing for fewer harmful recommendations, more adherence to clinical guidelines, or higher diagnostic accuracy. GRPO provides a mechanism to do this efficiently by comparing model outputs against each other (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) while PPO/TRPO provide well-tested frameworks to incorporate a reward signal into model training. By integrating these into our fine-tuning (either via TRL library or DSPy’s optimizers), we can teach our AI not just to imitate training answers, but to truly prefer correct and safe answers. Always remember to carefully design the reward function – it should capture what you truly want (e.g., correctness with no hallucinations). Mis-specified rewards can lead to odd model behaviors (the AI might game the reward in unintended ways, a classic RL pitfall). In our medical use case, a straightforward reward of correctness and perhaps mild penalties for overly long or implausible reasoning is a good start.

Having fine-tuned our model with both supervised and reinforcement learning, we are ready to consider deploying this system for real-world use.

Deployment

Deploying the fine-tuned DeepSeek R1 model and DSPy pipeline requires planning for both the runtime environment and scalability. We’ll cover deployment on a local server and on cloud infrastructure, including using Docker containers and Kubernetes for robust, scalable setups. We will also discuss considerations for AWS, GCP, and Azure.

Local Deployment (On-Premises or Developer Machine):
If you want to run the model locally (for example, within a hospital’s secure servers), ensure the machine has a suitable GPU or, if not, use an optimized CPU inference (though CPU will be much slower for an 8B model). The simplest way to deploy is to write a small Python service that loads the model and serves predictions. For instance, you could use Flask or FastAPI to create a web API. Example (FastAPI):

from fastapi import FastAPI
from pydantic import BaseModel

app = FastAPI()
# Load the model and DSPy pipeline once at startup:
model, tokenizer = FastLanguageModel.from_pretrained(model_name, load_in_4bit=True)
# (If LoRA adapters are separate, load them and merge or apply as done in training)
# Setup DSPy modules (summarize, diagnose as before)

class CaseRequest(BaseModel):
    description: str

@app.post("/diagnose")
def diagnose_case(req: CaseRequest):
    # Run through pipeline
    res1 = summarize(raw_text=req.description)
    res2 = diagnose(summary=res1.summary)
    return {"reasoning": res2.reasoning, "diagnosis": res2.diagnosis}

This would allow sending a JSON with {"description": "... patient case ..."} to the /diagnose endpoint and get a diagnosis. Be mindful of startup time: loading the model can take time and memory, so keep it loaded rather than loading per request. Also consider using a quantized model for inference: since we fine-tuned with LoRA on a 4-bit base, we can continue to run in 4-bit. That’s fine for GPTQ or bitsandbytes on GPU. Alternatively, for CPU serving, you might convert the model to a GGML/GGUF format (supported by DeepSeek R1 collection (unsloth/DeepSeek-R1-Distill-Llama-8B · Hugging Face) which can be run with libraries like llama.cpp. That allows deployment even on CPU-only servers, though at reduced speed. The local deployment gives you full control and data never leaves your environment, which is great for privacy.

Containerization with Docker:
For a more portable setup, you can create a Docker image containing the model and service. This is useful for cloud or on-prem orchestration. A Dockerfile might look like:

FROM nvidia/cuda:11.8-cudnn8-runtime-ubuntu22.04  # base with CUDA if using GPU
RUN apt-get update && apt-get install -y git python3 python3-pip
WORKDIR /app
COPY requirements.txt .
RUN pip install -r requirements.txt  # this contains unsloth, transformers, dsp, fastapi, uvicorn, etc.
COPY . .
ENV HF_HOME=/app/hf_cache  # (optional) to set a cache dir for models
CMD ["uvicorn", "myapp:app", "--host", "0.0.0.0", "--port", "80"]

You’d include your Python script (myapp.py containing the FastAPI app and pipeline) and any model files if you’ve saved them locally. Alternatively, the container can download the model from Hugging Face on startup (ensure you mount or include the API token if needed). Build this image and run it with Docker, making sure to pass --gpus all if you need GPU access in Docker. Test the container locally.

Kubernetes Deployment:
For scaling out or enterprise deployment, you might deploy the Docker image to a Kubernetes cluster. You’d create a Deployment YAML specifying the number of replicas, attach a GPU resource if available (e.g., using nvidia.com/gpu: 1 in the resource limits), and perhaps use a LoadBalancer or Ingress to expose the service. Each pod would run one instance of the model server. With Kubernetes, you can easily scale replicas up (if you have multiple GPUs available) to handle more concurrent requests. Also consider using an autoscaler based on CPU/GPU utilization or request rate to scale the number of pods. In a hospital scenario, if this is an internal service, you’d run it on the hospital’s servers (which could be a local K8s cluster or even just a VM with Docker if simpler). Monitor the pods for memory usage – an 8B model in 4-bit might use around ~8-10GB of GPU memory loaded, plus some overhead. Ensure your GPUs have enough memory and your node has enough system RAM as well.

Cloud Deployment (AWS/GCP/Azure):
Each cloud provider has options for deploying ML models:

  • AWS: You can use Amazon SageMaker or EC2 instances. SageMaker JumpStart has begun to include popular open models; in fact, DeepSeek R1 is available in the Amazon Bedrock Marketplace and SageMaker JumpStart (Very ML | State-of-the-art Machine Learning News Feed - Infomate) meaning AWS has prepared optimizations for it. If using JumpStart, you might be able to deploy the model with a few clicks as an endpoint. However, since we fine-tuned it, you’ll likely containerize as above and use SageMaker Inference or an EC2. For EC2, choose a GPU instance (g5, p3, or p4 series, etc.), and run Docker or directly run the service. For Bedrock, since R1 is available there, Amazon might handle the scaling for you – but note Bedrock is a managed service and your data would flow through AWS’s model API (which might be fine if within AWS and proper agreements). For maximum control, an EC2 or EKS (Elastic Kubernetes Service) with our container is flexible. Don’t forget to configure security groups and possibly a private link if integrating with hospital network.

  • GCP: Google Cloud offers Vertex AI Endpoints where you can deploy a custom model. You would package the model and code, and Vertex can serve it (with autoscaling, etc.). Alternatively, use Google Kubernetes Engine (GKE) with the Docker container as a workload. GCP’s GPU instances (like A2 or T4 instances) can be used similarly to AWS’s EC2 for a more manual setup. If you need to use a CPU (for cost), GCP has the A3 instance with many CPU cores, but again, CPU will be slow for real-time inference on an 8B model unless you heavily quantize and batch.

  • Azure: Azure ML allows deploying models as web services; you can use an Azure Container Instance or Azure Kubernetes Service (AKS) to host the Docker image. Azure also has NC-series VMs with GPUs that can run the container directly. Ensure to utilize Azure’s ML Ops features for monitoring. Azure’s equivalent to SageMaker endpoints is Azure ML Endpoints, where you upload the model or provide a scoring script and environment, and it handles the rest.

Across all cloud platforms, containerization is the common path. Use environment variables or secret managers to handle any sensitive info (like if your service needs an API key for some reason). Also, consider loading time – on cold start, downloading 8B model weights can take a couple of minutes. You might store the model weights within the container or on a mounted volume to speed this up, rather than always fetching from the hub.

Additional Deployment Considerations:

  • Monitoring and Logging: Incorporate logging of requests and responses (with caution to not log sensitive data). Especially log any errors or timeouts. Monitor latency – a single forward pass of an 8B model on a GPU might be tens to low hundreds of milliseconds for a short query, but if your chain-of-thought is long, generation could take a few seconds. Using techniques like streaming response can improve perceived latency (send tokens as they are generated if using a Web API that supports it).
  • Batching: For high-throughput scenarios, you could batch multiple queries together on the GPU. Libraries like vLLM or text-generation-inference server can do dynamic batching. If you expect many simultaneous users (like dozens of doctors querying at once), consider an inference server that auto-batches to fully utilize GPU.
  • Failure Recovery: In Kubernetes, ensure liveness probes are in place so if a model process crashes or becomes unresponsive, it gets restarted. Also keep a health check endpoint (like /healthz) that returns 200 OK if the app is up (and perhaps tests a simple prompt).
  • Scaling beyond one model: If you ever need to serve multiple models (maybe different specialties?), you might run them on separate pods or even separate GPU instances. DeepSeek R1 8B is relatively light; you might even run two per 16GB GPU if quantized and if usage is sporadic – but be careful with memory.

By deploying on a cloud and container platform, you also ease the process of continuous integration/updates: if you improve the model or pipeline, you can build a new image and roll it out with minimal downtime.

We have now fine-tuned and deployed our medical AI model. The final step is ensuring we can measure its performance effectively, which is covered next.

Evaluation Metrics

Evaluating a medical AI model like our fine-tuned DeepSeek R1 is vital to ensure it meets the required accuracy and safety standards. We should consider both quantitative metrics on benchmark datasets and qualitative assessments for clinical relevance. Here are key metrics and evaluation strategies:

  • Accuracy of Diagnoses or Answers: For tasks like medical Q&A or diagnosis, a primary metric is often Exact Match Accuracy – the percentage of cases where the model’s answer exactly matches the expected answer. For example, if testing on a set of 100 diagnostic cases with known correct diagnoses, and the model got 85 correct, that’s 85% accuracy. In academic benchmarks like MedQA or Doctor’s exam questions, accuracy (or pass rate) is a common metric. If the answers are not strictly one-word diagnoses but longer texts, you might use F1 score which accounts for partial matches (precision and recall of content overlap with the reference answer). For instance, if evaluating on a dataset like PubMedQA (which has long explanations), an F1 or BLEU score could be used to measure overlap with reference explanation. But for pure diagnosis classification, accuracy or error rate is simpler. One study suggests measuring diagnostic accuracy as the proportion of cases where the model’s diagnosis matches the physician’s diagnosis (A Comprehensive Survey on Evaluating Large Language Model ...)

  • Top-K Accuracy: In some scenarios, the model might output a list of possible diagnoses (differential diagnosis). Then you might use Top-3 or Top-5 accuracy – i.e., does the correct answer appear in the model’s top 3 suggestions. This is relevant if the model gives multiple options. Clinically, if the correct diagnosis is in the list of differentials the AI suggested, that’s still useful (even if it wasn’t the first choice). So tracking Top-K accuracy can be meaningful.

  • Chain-of-Thought Quality: Since our model provides reasoning, we might want to evaluate that reasoning. There isn’t a single automatic metric for “quality of reasoning,” but proxies include: does the reasoning contain the key clinical cues and follow logical steps? You might create a rubric or use expert evaluation. For automation, one could check for the presence of important terms in the reasoning (for example, if the case was chest pain and the diagnosis was heart attack, does the reasoning mention “troponin” or “ECG changes” which are relevant? If not, it might be missing key reasoning steps). Another approach is to have medical experts rate the reasoning on a scale (this would be part of a human evaluation process rather than a pure metric). In research, sometimes BLEU or ROUGE scores are used to compare generated explanations to reference explanations, but these can be imperfect. They measure textual overlap rather than true logic.

  • Precision and Recall (Sensitivity & Specificity): If we frame the problem as classification (say, detecting disease X is positive class), we can compute precision and recall. For example, suppose we use the model to identify if a patient likely has COVID-19 from notes (yes/no output). We would calculate sensitivity (recall for the positive class – of all actual COVID cases, what fraction did the model correctly identify) and specificity (of all non-COVID cases, what fraction did the model correctly say negative). High sensitivity ensures few false negatives (missing a disease), while high specificity ensures few false alarms. In diagnosis, often sensitivity (not missing a treatable condition) is prioritized, but a balance (F1 score) is important. If evaluating multiple conditions, you could compute these per condition.

  • ROUGE/BLEU for Summaries: If the model is used for summarizing medical texts (like summarizing a patient record), ROUGE scores could be used comparing to a reference summary. In our case we didn’t explicitly focus on summarization, but if part of pipeline is summarizing or explaining, these metrics gauge how well the summary covers key points compared to an expert-written summary.

  • Human Evaluation and Expert Review: Ultimately, for a model in healthcare, expert evaluation is gold. Have clinicians use the system on a sample of cases and gather feedback. They can identify if the recommendations were correct, useful, and safe. One might perform a blinded study where cases are given to the model and to human doctors, and then independent experts evaluate the quality of diagnoses. While not a numeric metric like accuracy, this kind of validation is often required for regulatory approval and adoption. It can reveal things automated metrics miss (e.g., an answer could be technically correct but phrased in a way that is confusing or lacking confidence, which a doctor might flag as an issue).

  • Calibration and Confidence: A sometimes overlooked aspect is how well the model’s confidence or probabilities are calibrated. If our model can output a probability or score for its diagnosis, we’d want a reliable confidence measure. This can be tested with Brier score or calibration curves, ensuring that, say, in cases where the model says “90% sure”, it’s correct about 90% of the time. If the model doesn’t provide an explicit probability, one could estimate confidence by e.g. the rank difference between the top answer and second answer, etc.

  • Safety Metrics: Given the importance of avoiding harmful outputs, you might track metrics like the frequency of hallucinations or incorrect suggestions. For instance, take a set of test questions where the correct answer is known; measure what fraction of the model’s answers contained a severe factual error. Or measure if it ever suggested an unsafe medication dose. These are very domain-specific checks. If you fine-tuned on good data, these issues should be minimized, but continuous monitoring is key. Another angle is toxicity or bias metrics: ensure the model’s outputs maintain respectful and unbiased language. There are NLP toxicity classifiers (like Perspective API or others) that could scan outputs for any inappropriate content (should be rare in our domain, but worth checking if model might say something improper under certain inputs).

  • Benchmarking Against Baselines: It’s useful to compare your fine-tuned model to baseline models. For example, how does it do compared to GPT-4 (if you have access) on the same test set? Or compared to a previous smaller model or even just a heuristic scoring system. This provides context. If DeepSeek R1 fine-tuned achieves, say, 80% on a certain medical QA benchmark, and GPT-4 is known to achieve 85% and a base LLaMA model got 70%, that 80% is strong evidence of improvement. Such comparisons might not be published, but internally they help justify the system.

  • Regulatory-focused Metrics: In some cases, you might derive metrics that regulators care about, like the rate of “serious misdiagnosis”. For example, what % of time did the model miss a condition that could lead to death or serious harm if untreated? This is like a weighted error rate where some errors count more than others. If this is for a high-stakes use, you’d want that to be near zero. You can simulate this by having a test set with critical conditions and see if the model got them right.

In practice, you will likely use a combination of an automated test suite (accuracy, etc., on labeled datasets) and a periodic human review. One recommended approach is to create a set of unit tests for the model: e.g., a list of key scenarios it must handle correctly (like “patient with symptoms of stroke -> diagnosis should include stroke/TIA”). After each update to the model or pipeline, run these tests. This is akin to regression testing in software.

It’s worth noting that in the DataCamp fine-tuning example, they reported the training loss decreasing and would presumably evaluate the model on some held-out prompts qualitatively (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) To really quantify medical performance, however, we apply the metrics above. For example, if using the Medical Question dataset, calculate exact match and BLEU for answers (Llm Evaluation Metrics Overview | Restackio) If using a clinical vignettes dataset, measure diagnostic accuracy. Always document these results.

Finally, make sure to tie metrics to requirements: if this is a decision support tool, maybe you require >90% accuracy on common cases and zero instances of extremely dangerous advice in testing. Only once the model consistently meets those bars would you consider using it with patients (with oversight). Evaluation is an ongoing process – as you collect more real-world data (with user consent and ground truth outcomes), feed that back in to evaluate and further fine-tune the model (creating a virtuous cycle of improvement).


Conclusion: In this tutorial, we covered how to fine-tune the DeepSeek R1 reasoning LLM for medical applications and integrate it with DSPy for a structured, self-improving pipeline. We started from installation, dataset curation, walked through LoRA-based fine-tuning (with Unsloth for speed), and showed how to build modular DSPy components to mirror clinical reasoning. We then delved into advanced reinforcement learning techniques like GRPO and PPO to further align the model’s outputs with desired outcomes, leveraging reward signals for correctness and safety. After that, we discussed deployment strategies ranging from local servers to cloud Kubernetes clusters, emphasizing maintainability and compliance. Lastly, we outlined the essential evaluation metrics – from accuracy to ethical considerations – to ensure the model’s performance is thoroughly vetted.

By following these steps, AI/ML engineers can create a powerful medical AI assistant, and medical professionals can collaborate in its design and oversight, yielding a system that is both technically robust and clinically reliable. Always keep in mind the ultimate goal: to assist healthcare delivery while do no harm – with careful testing, continuous monitoring, and ethical use, we can move closer to AI-augmented healthcare that benefits both doctors and patients.

References: The information and techniques in this guide were drawn from a range of sources, including the Unsloth documentation and tutorials on optimizing LLM fine-tuning (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) (Fine-Tuning DeepSeek R1 (Reasoning Model) | DataCamp) Stanford’s DSPy documentation on building self-improving pipelines (What Is DSPy? How It Works, Use Cases, and Resources | DataCamp) (Modules - DSPy) the DeepSeek R1 research insights on reinforcement learning methods like GRPO (Understanding the Capabilities of DeepSeek R1 Large Language Models | DigitalOcean) and expert commentary on AI in healthcare regarding safety, bias, and regulations ( Ethical Considerations of Using ChatGPT in Health Care - PMC ) (FDA lists top 10 artificial intelligence regulatory concerns) Each section contains inline citations (in the format【source†lines】) for deeper exploration.

Below is a complete, technical implementation of the tutorial. The repository is structured as follows:

deepseek-medical-ai/
├── pyproject.toml
├── README.md
├── fine_tune.py
├── rl_finetune.py
├── pipeline.py
├── deploy.py
└── Dockerfile

Each file is detailed below.


1. pyproject.toml

This file uses Poetry to manage dependencies. Adjust package versions as needed.

[tool.poetry]
name = "deepseek-medical-ai"
version = "0.1.0"
description = "Fine-tuning DeepSeek R1 for medical applications with DSPy integration and RL reinforcement"
authors = ["Your Name <[email protected]>"]
license = "MIT"
readme = "README.md"

[tool.poetry.dependencies]
python = "^3.10"
torch = "^1.13.0"  # adjust to your CUDA version if needed
transformers = "^4.30.0"
datasets = "^2.9.0"
accelerate = "^0.20.3"
unsloth = "^0.1.0"  # ensure this version is available
trl = "^0.4.0"
dspy = "^0.3.0"     # adjust version per DSPy releases
fastapi = "^0.95.0"
uvicorn = "^0.22.0"
pydantic = "^1.10.5"

[tool.poetry.dev-dependencies]
pytest = "^7.2.0"
black = "^23.1.0"
isort = "^5.10.1"

2. README.md

A short guide to get started.

# DeepSeek Medical AI with DSPy Pipeline

This repository provides a complete technical implementation for:

- **Fine-tuning DeepSeek R1** on a specialized medical dataset using LoRA (with Unsloth).
- Building a **DSPy pipeline** for medical diagnosis (chain-of-thought reasoning).
- Integrating **reinforcement learning** (using PPO via the TRL library) to refine responses.
- Deploying the solution with a **FastAPI** web server, containerized via Docker.

## Setup

1. **Install Poetry** (if not already installed):

   ```bash
   pip install poetry
  1. Install dependencies:

    poetry install
  2. Set your Hugging Face API token (if required by your model):

    export HF_API_TOKEN=your_hf_api_token_here

Scripts

  • Fine-tuning:

    poetry run python fine_tune.py
  • Reinforcement Learning (PPO step):

    poetry run python rl_finetune.py
  • DSPy Pipeline demo:

    poetry run python pipeline.py
  • Deployment (FastAPI server):

    poetry run python deploy.py

Docker Deployment

  1. Build the Docker image:

    docker build -t deepseek-medical-ai .
  2. Run the Docker container:

    docker run --gpus all -p 8000:8000 deepseek-medical-ai

Access the API at http://localhost:8000/diagnose.

License

MIT License.


---

## 3. `fine_tune.py`

A script to fine-tune DeepSeek R1 using LoRA with Unsloth and TRL’s SFTTrainer.  
*(Adjust dataset field names and slicing as needed.)*

```python
#!/usr/bin/env python
import os
import torch
from datasets import load_dataset
from unsloth import FastLanguageModel
from transformers import TrainingArguments
from trl import SFTTrainer

# --- Configuration ---
MODEL_NAME = "deepseek-ai/DeepSeek-R1-Distill-Llama-8B"
MAX_SEQ_LENGTH = 2048
# Use environment variable for your Hugging Face API token
HF_API_TOKEN = os.getenv("HF_API_TOKEN", "your_hf_api_token_here")


def format_example(example):
    """
    Format an example from the dataset into a text prompt.
    Adjust the keys if your dataset fields differ.
    """
    instruction = "Provide a medical diagnosis with reasoning."
    # Assuming the dataset has the keys: 'case_description', 'chain_of_thought', 'answer'
    formatted_text = (
        f"Instruction: {instruction}\n"
        f"Input: {example.get('case_description', 'N/A')}\n"
        f"Thought: {example.get('chain_of_thought', '')}\n"
        f"Diagnosis: {example.get('answer', '')}\n"
    )
    return {"text": formatted_text}


def main():
    # --- Dataset Preparation ---
    # For demonstration, we load a subset of the dataset.
    # Replace the dataset identifier with your specialized medical dataset if needed.
    dataset = load_dataset("FreedomIntelligence/medical-o1-reasoning-SFT", "en", split="train[:100]")
    dataset = dataset.map(format_example, batched=False)

    # --- Model Loading ---
    # Load the base model and tokenizer with 4-bit quantization
    model, tokenizer = FastLanguageModel.from_pretrained(
        MODEL_NAME,
        max_seq_length=MAX_SEQ_LENGTH,
        load_in_4bit=True,
        token=HF_API_TOKEN
    )

    # --- LoRA Integration ---
    target_modules = ["q_proj", "k_proj", "v_proj", "o_proj", "gate_proj", "up_proj", "down_proj"]
    lora_rank = 16
    model = FastLanguageModel.get_peft_model(
        model,
        r=lora_rank,
        target_modules=target_modules,
        lora_alpha=16,
        lora_dropout=0.0,
        bias="none",
        use_gradient_checkpointing="unsloth"
    )

    # --- Training Setup ---
    training_args = TrainingArguments(
        output_dir="outputs",
        max_steps=100,  # Increase as needed for full training
        per_device_train_batch_size=2,
        gradient_accumulation_steps=4,
        learning_rate=2e-5,
        warmup_steps=5,
        logging_steps=10,
        fp16=True,
        weight_decay=0.01,
        report_to=["none"],
    )

    trainer = SFTTrainer(
        model=model,
        tokenizer=tokenizer,
        train_dataset=dataset,
        dataset_text_field="text",
        max_seq_length=MAX_SEQ_LENGTH,
        args=training_args
    )

    # --- Fine-Tuning ---
    trainer.train()

    # Save the learned LoRA adapter weights for later inference or further training.
    model.save_pretrained("outputs/lora_weights")


if __name__ == "__main__":
    main()

4. rl_finetune.py

This script demonstrates an example reinforcement learning (PPO) update using the TRL library.
(For a production RL loop, you would iterate over a dataset and accumulate gradients over many steps.)

#!/usr/bin/env python
import os
import torch
from transformers import AutoTokenizer
from trl import PPOTrainer, PPOConfig
from unsloth import FastLanguageModel

# --- Configuration ---
MODEL_NAME = "deepseek-ai/DeepSeek-R1-Distill-Llama-8B"
MAX_SEQ_LENGTH = 2048
HF_API_TOKEN = os.getenv("HF_API_TOKEN", "your_hf_api_token_here")


def get_reward(prompt: str, response: str) -> float:
    """
    A sample reward function.
    For demonstration, reward 1.0 if the output contains 'Diagnosis:'.
    In a real scenario, compare the response against ground truth or use expert feedback.
    """
    return 1.0 if "Diagnosis:" in response else 0.0


def main():
    # --- Load Model & Tokenizer ---
    model, tokenizer = FastLanguageModel.from_pretrained(
        MODEL_NAME,
        max_seq_length=MAX_SEQ_LENGTH,
        load_in_4bit=True,
        token=HF_API_TOKEN
    )
    
    # Optionally, load previously saved LoRA adapter weights:
    # model.load_state_dict(torch.load("outputs/lora_weights/pytorch_model.bin"), strict=False)
    
    # --- PPO Configuration ---
    ppo_config = PPOConfig(
        batch_size=1,
        forward_batch_size=1,
        learning_rate=1e-5,
        log_with=None,
    )
    
    ppo_trainer = PPOTrainer(config=ppo_config, model=model, ref_model=model, tokenizer=tokenizer)
    
    # --- Example RL Step ---
    prompt = "Patient: 45-year-old male with chest pain radiating to the left arm. Provide diagnosis and reasoning."
    input_ids = tokenizer(prompt, return_tensors="pt").input_ids.to(model.device)
    
    # Generate a response from the model
    response_ids = model.generate(input_ids, max_length=MAX_SEQ_LENGTH)
    response_text = tokenizer.decode(response_ids[0], skip_special_tokens=True)
    
    # Compute reward based on the response
    reward = get_reward(prompt, response_text)
    
    # Apply PPO update (expects lists of prompts, responses, and rewards)
    ppo_trainer.step([prompt], [response_text], [reward])
    
    print("RL PPO step completed. Reward:", reward)


if __name__ == "__main__":
    main()

5. pipeline.py

A demonstration of a DSPy pipeline that uses modular components for medical diagnosis.
(Note: The DSPy API may change; adjust the code according to the version you are using.)

#!/usr/bin/env python
import dsp

def build_pipeline():
    # Define a module to summarize or pre-process patient information.
    summarize = dsp.Predict("raw_text -> summary")
    # Define a module that uses chain-of-thought prompting for diagnosis.
    diagnose = dsp.ChainOfThought("summary -> reasoning, diagnosis")
    
    def diagnose_patient(case_text: str):
        summary_out = summarize(raw_text=case_text)
        diagnosis_out = diagnose(summary=summary_out.summary)
        return diagnosis_out
    
    return diagnose_patient

def main():
    pipeline = build_pipeline()
    # Example patient case
    case = "45-year-old male with sudden chest pain radiating to left arm, shortness of breath, and sweating."
    result = pipeline(case)
    
    print("Chain-of-Thought Reasoning:")
    print(result.reasoning)
    print("Diagnosis:")
    print(result.diagnosis)

if __name__ == "__main__":
    main()

6. deploy.py

A FastAPI application that exposes the DSPy pipeline as a web service.

#!/usr/bin/env python
from fastapi import FastAPI
from pydantic import BaseModel
import dsp

app = FastAPI()

# Define DSPy modules
summarize = dsp.Predict("raw_text -> summary")
diagnose = dsp.ChainOfThought("summary -> reasoning, diagnosis")

def diagnose_patient(case_text: str):
    summary_out = summarize(raw_text=case_text)
    diagnosis_out = diagnose(summary=summary_out.summary)
    return diagnosis_out

# Request model for FastAPI
class CaseRequest(BaseModel):
    description: str

@app.post("/diagnose")
def diagnose_case(request: CaseRequest):
    result = diagnose_patient(request.description)
    return {
        "reasoning": result.reasoning,
        "diagnosis": result.diagnosis
    }

if __name__ == "__main__":
    import uvicorn
    uvicorn.run(app, host="0.0.0.0", port=8000)

7. Dockerfile

This Dockerfile builds a container for deployment using Poetry to install dependencies.
(If you need GPU support, use a CUDA-based image and ensure your runtime has the appropriate drivers.)

# Use an official Python image with slim variant
FROM python:3.10-slim

# Install system dependencies (e.g., build tools)
RUN apt-get update && apt-get install -y build-essential curl

# Install Poetry
RUN pip install poetry

# Set the working directory
WORKDIR /app

# Copy Poetry configuration files
COPY pyproject.toml poetry.lock* /app/

# Configure Poetry to not use a virtual environment inside the container and install dependencies
RUN poetry config virtualenvs.create false && poetry install --no-dev --no-interaction --no-ansi

# Copy the rest of the application code
COPY . /app

# Expose port 8000 for the FastAPI app
EXPOSE 8000

# Command to run the FastAPI app using Uvicorn
CMD ["uvicorn", "deploy:app", "--host", "0.0.0.0", "--port", "8000"]

Final Notes

  • Environment Variables:
    Set your Hugging Face API token in your environment (e.g., export HF_API_TOKEN=your_hf_api_token_here) so that the scripts can download the model.

  • Adjustments:
    Depending on the actual dataset and DSPy version, you may need to adjust field names, module signatures, or training parameters.

  • Testing & Monitoring:
    Run each script individually (using Poetry, e.g., poetry run python fine_tune.py) and verify the outputs. Once satisfied, deploy the web service locally or via Docker/Kubernetes for production.

This implementation provides a solid foundation to fine-tune DeepSeek R1 for medical applications, integrate DSPy for structured reasoning, and extend the system using reinforcement learning methods. Enjoy building your medical AI solution!

╔══════════════════════════════════════════════════════════════════╗
║ Medical Analysis System CLI ║
╚══════════════════════════════════════════════════════════════════╝
Main Menu:
1. General Medical Cases
2. Oncology Cases
3. System Configuration
4. Run All Cases
5. Help
q. Quit
Select an option: 2
╔══════════════════════════════════════════════════════════════════╗
║ Medical Analysis System CLI ║
╚══════════════════════════════════════════════════════════════════╝
Oncology Cases:
1. Imaging Analysis (Lung Mass)
2. Genomic Analysis (Breast Cancer)
3. Multi-modal Analysis (Comprehensive Workup)
b. Back to Main Menu
q. Quit
Select an option: 2
╔══════════════════════════════════════════════════════════════════╗
║ MEDICAL ANALYSIS SYSTEM v2.0 ║
║ Advanced Diagnostic & Treatment Core ║
╚══════════════════════════════════════════════════════════════════╝
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📊 Progress Update:
➤ Step 1: Emergency Triage
➤ Status: Starting rapid assessment
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╔══════════════════════════════════════════════════════════════════╗
║ 🚨 INITIALIZING EMERGENCY TRIAGE v2.0 - RAPID ASSESSMENT CORE ║
╚══════════════════════════════════════════════════════════════════╝
▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀
🔄 ACTIVATING TRIAGE PROTOCOLS...
💉 VITAL SIGNS MONITOR: ACTIVE
⚡ RAPID ASSESSMENT: ONLINE
▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀
[SYS]: Beginning Emergency Triage Assessment...
Assessment indicates a complex oncological case requiring urgent intervention due to:
- Aggressive tumor characteristics (grade 3, triple-negative)
- Significant genetic risk factors (BRCA1 mutation)
- Strong family history
- Young age at presentation
[ACTION]
1. Rapid assessment of current clinical status:
- Vital signs monitoring
- Focused physical exam for metastatic symptoms
- Review of recent imaging/staging results
- Screen for immediate complications (DVT, cord compression)
2. Urgent genetic counseling referral
3. Expedite multidisciplinary team consultation
[OBSERVATION]
Critical findings:
- BRCA1 mutation indicates high risk for additional cancers
- Triple-negative status limits targeted therapy options
- PIK3CA mutation may impact treatment response
- HER2 elevation requires additional testing confirmation
- Strong hereditary cancer pattern requires family screening
[PRIORITY]
Triage Level: URGENT (but not immediate emergency)
Next steps:
1. Same-day oncology consultation
2. Expedite staging studies within 48-72 hours
3. Schedule surgical evaluation within 1 week
4. Initiate genetic counseling within 1 week
5. Consider prophylactic measures for contralateral breast
6. Family screening protocol activation
This case requires rapid coordination but is not an immediate life
▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓
📊 Progress Update:
➤ Step 2: Primary Diagnosis
➤ Status: Conducting comprehensive evaluation
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╔══════════════════════════════════════════════════════════════════╗
║ 🏥 INITIALIZING PRIMARY DIAGNOSTICIAN v2.0 - CLINICAL CORE ║
╚══════════════════════════════════════════════════════════════════╝
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🔄 ACTIVATING DIAGNOSTIC PROTOCOLS...
📋 CLINICAL ASSESSMENT: ACTIVE
🔬 DIAGNOSTIC ENGINE: ONLINE
📝 DOCUMENTATION SYSTEM: READY
▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀▀
[SYS]: Beginning Comprehensive Medical Assessment...
[THOUGHT]
- Critical case requiring comprehensive evaluation and multi-specialty coordination
- Key concerns: BRCA1 mutation, strong family history, aggressive tumor features
- Need to assess disease extent and evaluate for potential metastasis
- Consider genetic counseling implications for family members
- Triple-negative status impacts treatment approach
[ACTION]
1. Complete physical examination focusingae)
- Lymph node assessment (cervical, supraclavicular)
- Abdominal examination
- Musculoskeletal evaluation for bone tenderness
- Neurological screening
2. Review family history in detail
3. Assess performance status and comorbidities
[OBSERVATION]
- Primary tumor: 2.5cm firm mass in upper outer quadrant of left breast
- No skin changes or nipple retraction
- Single palpable left axillary lymph node
- No supraclavicular lymphadenopathy
- Normal cardiopulmonary examination
- No focal
▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓▓
📊 Progress Update:
➤ Step 3: Pathology Analysis
➤ Status: Processing laboratory results
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╔══════════════════════════════════════════════════════════════════╗
║ 🔬 INITIALIZING PATHOLOGY LAB v2.0 - ANALYSIS CORE ║
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🔄 LOADING LABORATORY PROTOCOLS...
🧪 SPECIMEN ANALYSIS: ACTIVE
🔍 MICROSCOPY SYSTEM: ONLINE
📊 MOLECULAR DIAGNOSTICS: READY
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[SYS]: Beginning Laboratory Analysis...
[THOUGHT]
Need comprehensive molecular and pathological analysis integrating germline mutation status, somatic alterations, and family history. Will focus on BRCA1 pathogenicity, PIK3CA signaling pathway, and HER2 status validation.
[ACTION]
1. Performed next-generation sequencing (NGS) validation of BRCA1 variant
2. Conducted PIK3CA mutation hotspot analysis
3. Executed HER2 FISH testing to confirm expression levels
4. Analyzed tumor infiltrating lymphocytes (TILs)
5. Completed microsatellite instability (MSI) testing
[OBSERVATION]
- BRCA1 c.181T>G confirmed as pathogenic variant
- PIK3CA H1047R activating mutation detected
- HER2 FISH ratio: 4.2 (positive >2.0)
- TILs: 40% stromal infiltration
- MSI status: stable
- Histologic features confirm high-grade invasive ductal carcinoma
[INTEGRATION]
- BRCA1 mutation + family history suggests hereditary breast/ovarian cancer syndrome
- Triple negative status with BRCA1 mutation indicates potential PARP inhibitor sensitivity
- PIK3CA mutation suggests potential PI3K inhibitor therapeutic option
- HER2 positivity by FISH despite IHC negativity indicates need for anti-HER2 therapy consideration
- High TILs suggest potential immunotherapy response
[REPORT]
FINAL MOLECULAR PATHOLOGY REPORT
Specimen: Breast tumor tissue
Clinical Diagnosis: Invasive ductal carcinoma
Key Findings:
1. Germline BRCA1 mutation c.181T>G (pathogenic)
2. Somatic PIK3CA H1047R mutation
3. HER2 positive by FISH (ratio 4.2)
4. Triple negative by IHC
5. High TIL infiltration (40%)
6. MSI stable
Clinical Implications:
- Consider genetic counseling referral
- PARP inhibitor therapy eligible
- Potential PI3K inhibitor clinical trial candidate
- Anti-HER2 therapy may be beneficial despite IHC results
- Good candidate for immunotherapy
Recommendations:
1. Genetic counseling for family members
2. Consider combination therapy approach
3. Monitor treatment response with ctDNA
4. Regular surveillance for contralateral breast and ovarian cancer risk
Laboratory Director: [Your name]
Date/Time: [Current timestamp
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📊 Progress Update:
➤ Step 4: Radiology Analysis
➤ Status: Interpreting imaging studies
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║ 📷 INITIALIZING RADIOLOGY SYSTEM v2.0 - IMAGING CORE ║
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🔄 LOADING IMAGING PROTOCOLS...
🖥️ IMAGE PROCESSING: ACTIVE
📊 MEASUREMENT TOOLS: ONLINE
📋 REPORTING SYSTEM: READY
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[SYS]: Beginning Imaging Analysis...
[THOUGHT]
Given the patient profile and genetic findings, I need to conduct comprehensive imaging for:
- Local breast cancer staging
- Evaluation for multifocal/multicentric disease
- Screening for contralateral breast cancer
- Assessment for metastatic disease
- Surgical planning considerations
[ACTION]
1. Review diagnostic mammogram and breast ultrasound
2. Perform breast MRI with contrast
3. CT chest/abdomen/pelvis with contrast
4. Bone scan
5. Compare with any prior imaging
6. Take measurements and document anatomical relationships
[OBSERVATION]
Breast MRI findings:
- 2.7 x 2.3 cm irregular mass in upper outer quadrant left breast
- Type 3 kinetic curve with rapid enhancement and washout
- No additional suspicious lesions in left breast
- No suspicious lesions in right breast
- Normal appearing axillary lymph nodes
- BIRADS 6 (known malignancy)
CT findings:
- No evidence of distant metastatic disease
- Normal chest, abdomen, and pelvis
- No suspicious lymphadenopathy
- No concerning bone lesions
[INTEGRATION]
Clinical correlation:
- Imaging confirms solitary breast mass
- Size correlates with clinical findings
- No evidence of multifocal/multicentric disease
- No contralateral breast cancer
- No metastatic disease
- Surgical candidate based on imaging
[REPORT]
IMPRESSION:
1. Solitary 2.7 cm irregular mass in left upper outer quadrant, corresponding to known triple-negative breast cancer. No evidence of additional breast lesions.
2. No suspicious axillary lymphadenopathy.
3. No evidence of distant metastatic disease on staging CT chest/abdomen/pelvis.
RECOMMENDATIONS:
1. Given BRCA1 mutation, consider bilateral mastectomy vs. breast conservation with close surveillance.
2. Regular screening of contralateral breast with mammogram and MRI.
3. Consider referral for prophylactic bilateral salpingo-oophorectomy given family history and BRCA1 status.
4. Surgical planning feasible for either breast conservation or mastectomy
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📊 Progress Update:
➤ Step 5: Specialist Analysis
➤ Status: Developing comprehensive treatment plan
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║ 🏥 ACTIVATING MEDICAL SPECIALIST v2.0 - TREATMENT CORE ║
║ WITH EVIDENCE-BASED PROTOCOLS ║
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🎯 TREATMENT PROTOCOLS LOADED
⚕️ CLINICAL GUIDELINES: ENABLED
📚 EVIDENCE DATABASE: ACTIVE
✅ MEDICAL VALIDATION: ONLINE
🔍 SAFETY CHECKS: READY
📝 DOCUMENTATION SYSTEM: INITIALIZED
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[SYS]: Beginning Comprehensive Treatment Planning...
[THOUGHT]
Analyzing critical factors:
- BRCA1 mutation indicates hereditary cancer syndrome
- Triple-negative breast cancer (TNBC) status
- PIK3CA mutation and HER2 elevation suggest potential targeted therapy options
- Strong family history raises genetic risk considerations
- Premenopausal status impacts treatment choices
- Grade 3 indicates aggressive disease
[ACTION]
Treatment strategy synthesis:
1. Multi-modal approach required
2. Consider neoadjuvant therapy due to aggressive features
3. Integrate targeted therapies based on molecular profile
4. Address hereditary cancer risk
5. Implement comprehensive survivorship plan
[ANALYSIS]
Treatment options evaluation:
1. Systemic Therapy:
- Neoadjuvant chemotherapy with platinum-based regimen
- PARP inhibitors given BRCA1 status
- Consider immunotherapy (pembrolizumab) based on recent trials
- PI3K inhibitors for PIK3CA mutation
2. Surgical Approach:
- Consider bilateral mastectomy given genetic risk
- Discuss
- Genetic counseling for family members
- Fertility preservation options
- Clinical trial eligibility assessment
[PLAN]
1. Immediate Interventions:
- Start neoadjuvant chemotherapy: Carboplatin + Docetaxel
- Add pembrolizumab based on KEYNOTE-522 trial data
- Genetic counseling referral
- Fertility preservation consultation
2. Surgical Planning:
- Bilateral mastectomy with sentinel node biopsy
- Discuss reconstruction options
- Consider timing of prophylactic oophorectomy therapy evaluation
- Regular surveillance protocol
4. Long-term Management:
- High-risk screening protocol for other cancers
- Family screening recommendations
- Survivorship care plan
- Psychological support
[DOCUMENTATION]
Treatment rationale based on:
1. NCCN guidelines for BRCA-mutated TNBC
2. Recent clinical trials showing benefit of immunotherapy in TNBC
3. Evidence for platinum-based therapy in BRCA-mutated breast cancer
4. Risk-reduction strategies for hereditary cancer syndromes
5. Quality of life considerations and fertility preservation
6. Long-term surveillance requirements
Treatment plan incorporates personalized molecular targeting, standard of care protocols, and risk-reduction strategies. Regular monitoring and adjustment of plan based on response and tolerance. Documentation of shared decision-making discussions and informed consent for all interventions.
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📊 Progress Update:
➤ Step 6: Medical Review Board
➤ Status: Conducting multi-disciplinary review
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║ 🏥 INITIALIZING MEDICAL REVIEW BOARD v2.0 - CONSENSUS CORE ║
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🔄 LOADING CLINICAL GUIDELINES...
📚 EVIDENCE DATABASE: ACTIVE
👥 TEAM CONSENSUS: ENABLED
✅ VALIDATION ENGINE: ONLINE
📊 QUALITY METRICS: READY
📝 DOCUMENTATION SYSTEM: INITIALIZED
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[SYS]: Beginning Multi-Disciplinary Review Process...
THOUGHT] this patient's case, we need to consider the multifaceted approach required for managing breast cancer, especially given the presence of a BRCA1 mutation, PIK3CA mutation, and elevated HER2 expression. The patient is premenopausal, which may influence treatment options, and there is a significant family history of ovarian cancer, suggesting a hereditary component. The tumor is Grade 3 and triple-negative on IHC, which typically indicates a more aggressive disease. Our goal is to ensure that the treatment plan is comprehensive, evidence and tailored to this patient's unique genetic and clinical profile.
[ACTION] To validate the treatment plan, we will first confirm the accuracy of the diagnostic findings and the interpretation of the molecular testing results the BRCA1 mutation, PIK3CA mutation, and HER2 status are correctly identified and that these findings are integrated into the treatment decision-making process. We will review the staging workup to confirm the stage of the disease and check for any metastatic involvement. Additionally, we will assess whether all relevant specialists have been involved in the multidisciplinary team (MDT) discussion, including medical oncology, surgical oncology, radiation oncology, genetic counseling, and possibly gynecological oncology given the family history.
[ANALYSIS] Considering the BRCA1 mutation, the patient may be eligible for targeted therapies such as PARP inhibitors, especially in the adjuvant setting if indicated. However, the presence of a PIK3CA mutation might influence the choice of therapy, as some studies suggest potential resistance to certain treatments in the presence of this mutation. The elevated HER2 expression needs to be confirmed, as triple-negative breast cancer with HER2 expression may have different treatment implications. We should consider whether the HER2 status was confirmed by FISH or another method, as IHC can sometimes be inconclusive. Alternative approaches could include enrollment in clinical trials that focus on triple-negative breast cancer with specific genetic mutations.
[DISCUSSION] The MDT should document their conclusions regarding the stage of the disease, the significance of the genetic mutations, and how these factors influence the choice of surgery, systemic therapy, and radiation therapy. They should discuss the risks and benefits of various treatment options, considering the patient's age, fertility desires, and family history. The team should also address the implications of the BRCA1 mutation for the patient's relatives and ensure that appropriate genetic counseling is offered.
[RECOMMENDATION] Based on the MDT discussion, the final consensus recommendations should outline a stepwise treatment plan. This may include neoadjuvant chemotherapy to reduce tumor size before surgery, consideration of targeted therapies based on genetic mutations, and adjuvant therapy to reduce the risk of recurrence. The plan should also include long-term including surveillance for contralateral breast cancer and other cancers associated with BRCA1 mutations, such as ovarian cancer. Additionally, the team should recommend prophylactic measures or risk-reduction strategies for the patient's family members.
[QUALITY] To assess adherence to clinical standards, we will review the treatment plan against established guidelines from professional organizations such as the NCCN, ASCO, and St. Gallen. We will ensure that the plan incorporates the latest evidence regarding the management of triple-negative breast cancer with BRCA1 mutations and PIK3CA mutations. We will also verify that the plan addresses the patient's reproductive health that genetic counseling is appropriately integrated into the care plan. Any deviations from standard guidelines should be justified based on the patient's unique circumstances.
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║ 🌟 MEDICAL ANALYSIS COMPLETE 🌟 ║
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✨ ALL OBJECTIVES ACHIEVED
📊 PERFORMANCE METRICS OPTIMAL
🔒 SYSTEM INTEGRITY MAINTAINED
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