Specialized model for Clinical Entity Recognition - Clinical entities related to Chronic Lymphocytic Leukemia
Model Overview
This model is a state-of-the-art fine-tuned transformer engineered to deliver enterprise-grade accuracy for clinical entity recognition - clinical entities related to chronic lymphocytic leukemia. This specialized model excels at identifying and extracting biomedical entities from clinical texts, research papers, and healthcare documents, enabling applications such as drug interaction detection, medication extraction from patient records, adverse event monitoring, literature mining for drug discovery, and biomedical knowledge graph construction with production-ready reliability for clinical and research applications.
Key Features
- High Precision: Optimized for biomedical entity recognition
- Domain-Specific: Trained on curated CLL dataset
- Production-Ready: Validated on clinical benchmarks
- Easy Integration: Compatible with Hugging Face Transformers ecosystem
Supported Entity Types
This model can identify and classify the following biomedical entities:
Dataset
CLL corpus is specialized for chronic lymphocytic leukemia entity recognition in hematology and cancer research.
The CLL (Chronic Lymphocytic Leukemia) corpus is a domain-specific biomedical NER dataset focused on entities related to chronic lymphocytic leukemia, a type of blood cancer. This specialized corpus contains annotations for CLL-specific terminology, biomarkers, treatment entities, and clinical concepts relevant to hematology and oncology research. The dataset is designed to support the development of clinical NLP systems for leukemia research, hematological disorder analysis, and cancer informatics applications. It is particularly valuable for identifying disease-specific entities, therapeutic interventions, and prognostic factors mentioned in CLL research literature. The corpus serves as a benchmark for evaluating NER models in specialized medical domains and clinical research.
Performance Metrics
Current Model Performance
- F1 Score:
0.96
- Precision:
0.93
- Recall:
0.99
- Accuracy:
0.98
Comparative Performance on CLL Dataset
Rankings based on F1-score performance across all models trained on this dataset.
Figure: OpenMed (Open-Source) vs. Latest SOTA (Closed-Source) performance comparison across biomedical NER datasets.
Quick Start
Installation
pip install transformers torch
Usage
from transformers import pipeline
# Load the model and tokenizer
# Model: https://huggingface.co/OpenMed/OpenMed-NER-BloodCancerDetect-ElectraMed-560M
model_name = "OpenMed/OpenMed-NER-BloodCancerDetect-ElectraMed-560M"
# Create a pipeline
medical_ner_pipeline = pipeline(
model=model_name,
aggregation_strategy="simple"
)
# Example usage
text = "The patient presented with chronic lymphocytic leukemia symptoms."
entities = medical_ner_pipeline(text)
print(entities)
token = entities[0]
print(text[token["start"] : token["end"]])
NOTE: The aggregation_strategy parameter defines how token predictions are grouped into entities. For a detailed explanation, please refer to the Hugging Face documentation.
Here is a summary of the available strategies:
- none: Returns raw token predictions without any aggregation.
- simple: Groups adjacent tokens with the same entity type (e.g., B-LOC followed by I-LOC).
- first: For word-based models, if tokens within a word have different entity tags, the tag of the first token is assigned to the entire word.
- average: For word-based models, this strategy averages the scores of tokens within a word and applies the label with the highest resulting score.
- max: For word-based models, the entity label from the token with the highest score within a word is assigned to the entire word.
Batch Processing
For efficient processing of large datasets, use proper batching with the batch_size parameter:
texts = [
"The patient presented with chronic lymphocytic leukemia symptoms.",
"B-cell proliferation was observed in bone marrow samples.",
"Treatment with ibrutinib showed promising results.",
"Flow cytometry confirmed the diagnosis of chronic lymphocytic leukemia.",
"The patient had del(17p), a high-risk feature in CLL.",
]
# Efficient batch processing with optimized batch size
# Adjust batch_size based on your GPU memory (typically 8, 16, 32, or 64)
results = medical_ner_pipeline(texts, batch_size=8)
for i, entities in enumerate(results):
print(f"Text {i+1} entities:")
for entity in entities:
print(f" - {entity['word']} ({entity['entity_group']}): {entity['score']:.4f}")
Large Dataset Processing
For processing large datasets efficiently:
from transformers.pipelines.pt_utils import KeyDataset
from datasets import Dataset
import pandas as pd
# Load your data
# Load a medical dataset from Hugging Face
from datasets import load_dataset
# Load a public medical dataset (using a subset for testing)
medical_dataset = load_dataset("BI55/MedText", split="train[:100]") # Load first 100 examples
data = pd.DataFrame({"text": medical_dataset["Completion"]})
dataset = Dataset.from_pandas(data)
# Process with optimal batching for your hardware
batch_size = 16 # Tune this based on your GPU memory
results = []
for out in medical_ner_pipeline(KeyDataset(dataset, "text"), batch_size=batch_size):
results.extend(out)
print(f"Processed {len(results)} texts with batching")
Performance Optimization
Batch Size Guidelines:
- CPU: Start with batch_size=1-4
- Single GPU: Try batch_size=8-32 depending on GPU memory
- High-end GPU: Can handle batch_size=64 or higher
- Monitor GPU utilization to find the optimal batch size for your hardware
Memory Considerations:
# For limited GPU memory, use smaller batches
medical_ner_pipeline = pipeline(
model=model_name,
aggregation_strategy="simple",
device=0 # Specify GPU device
)
# Process with memory-efficient batching
for batch_start in range(0, len(texts), batch_size):
batch = texts[batch_start:batch_start + batch_size]
batch_results = medical_ner_pipeline(batch, batch_size=len(batch))
results.extend(batch_results)
Dataset Information
- Dataset: CLL
- Description: Clinical Entity Recognition - Clinical entities related to Chronic Lymphocytic Leukemia
Training Details
- Base Model: multilingual-e5-large-instruct
- Training Framework: Hugging Face Transformers
- Optimization: AdamW optimizer with learning rate scheduling
- Validation: Cross-validation on held-out test set
Model Architecture
- Base Architecture: multilingual-e5-large-instruct
- Task: Token Classification (Named Entity Recognition)
- Labels: Dataset-specific entity types
- Input: Tokenized biomedical text
- Output: BIO-tagged entity predictions
Use Cases
This model is particularly useful for:
- Clinical Text Mining: Extracting entities from medical records
- Biomedical Research: Processing scientific literature
- Drug Discovery: Identifying chemical compounds and drugs
- Healthcare Analytics: Analyzing patient data and outcomes
- Academic Research: Supporting biomedical NLP research
License
Licensed under the Apache License 2.0. See LICENSE for details.
Contributing
We welcome contributions of all kinds! Whether you have ideas, feature requests, or want to join our mission to advance open-source Healthcare AI, we'd love to hear from you.
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Citation
If you use this model in your research or applications, please cite the following paper:
@misc{panahi2025openmedneropensourcedomainadapted,
title={OpenMed NER: Open-Source, Domain-Adapted State-of-the-Art Transformers for Biomedical NER Across 12 Public Datasets},
author={Maziyar Panahi},
year={2025},
eprint={2508.01630},
archivePrefix={arXiv},
primaryClass={cs.CL},
url={https://arxiv.org/abs/2508.01630},
}
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