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Vinicius Anjos de Almeida

Publications and source records attributed to Vinicius Anjos de Almeida.

3 recordsLinked to original sources

Agentic systems for breast cancer treatment recommendations

Large language models (LLMs) are increasingly being explored for clinical decision support, but their reliability in complex oncology treatment planning remains unclear. We evaluated agentic LLM systems for breast cancer treatment recommendation generation using 72 real clinical cases across stages I to IV and 1,147 case-specific rubrics generated through Asymmetric Information Rubric Generation (AIRG), in which the rubric generator had access to real clinical decisions unavailable to the evaluated models. Seven pipelines were compared, including single-LLM baselines, tool-augmented systems, and multi-agent architectures with fact checking and autonomous subagent spawning. The best-performing configuration, Claude Opus 4.8 with the D&C+SA pipeline, achieved a global score of 0.594 $\pm$ 0.025. Tool use and increased agent autonomy had mixed effects, improving performance in some settings but degrading it in others. Performance varied by clinical domain and disease stage, and oncologist-led error analysis revealed persistent clinically relevant failures, including incorrect or missing recommendations, flawed justifications, citation errors, outdated claims, and overconfidence. These findings suggest that agentic LLM systems can generate clinically relevant breast cancer recommendations, but remain insufficient for unsupervised clinical use.

cs.CL↗

Clinical named entity recognition in the Portuguese language: a benchmark of modern BERT models and LLMs

Clinical notes contain valuable unstructured information. Named entity recognition (NER) enables the automatic extraction of medical concepts; however, benchmarks for Portuguese remain scarce. In this study, we aimed to evaluate BERT-based models and large language models (LLMs) for clinical NER in Portuguese and to test strategies for addressing multilabel imbalance. We compared BioBERTpt, BERTimbau, ModernBERT, and mmBERT with LLMs such as GPT-5 and Gemini-2.5, using the public SemClinBr corpus and a private breast cancer dataset. Models were trained under identical conditions and evaluated using precision, recall, and F1-score. Iterative stratification, weighted loss, and oversampling were explored to mitigate class imbalance. The mmBERT-base model achieved the best performance (micro F1 = 0.76), outperforming all other models. Iterative stratification improved class balance and overall performance. Multilingual BERT models, particularly mmBERT, perform strongly for Portuguese clinical NER and can run locally with limited computational resources. Balanced data-splitting strategies further enhance performance.

cs.CL↗

Large Language Models as Medical Codes Selectors: a benchmark using the International Classification of Primary Care

Background: Medical coding structures healthcare data for research, quality monitoring, and policy. This study assesses the potential of large language models (LLMs) to assign ICPC-2 codes using the output of a domain-specific search engine. Methods: A dataset of 437 Brazilian Portuguese clinical expressions, each annotated with ICPC-2 codes, was used. A semantic search engine (OpenAI's text-embedding-3-large) retrieved candidates from 73,563 labeled concepts. Thirty-three LLMs were prompted with each query and retrieved results to select the best-matching ICPC-2 code. Performance was evaluated using F1-score, along with token usage, cost, response time, and format adherence. Results: Twenty-eight models achieved F1-score > 0.8; ten exceeded 0.85. Top performers included gpt-4.5-preview, o3, and gemini-2.5-pro. Retriever optimization can improve performance by up to 4 points. Most models returned valid codes in the expected format, with reduced hallucinations. Smaller models (<3B) struggled with formatting and input length. Conclusions: LLMs show strong potential for automating ICPC-2 coding, even without fine-tuning. This work offers a benchmark and highlights challenges, but findings are limited by dataset scope and setup. Broader, multilingual, end-to-end evaluations are needed for clinical validation.

cs.CL↗