This work introduces OpenMTB-Audit, an open-source benchmark of 500 synthetic non-small cell lung cancer cases spanning five adversarial error categories and four safety labels, and developed MTB-AuditAgent, a deterministic seven-module framework separating evidence verification, missing-information detection, safety classification, and abstention.
Abstract
Molecular tumor boards integrate genomic findings, clinical context, and therapeutic evidence to support precision oncology. As AI enters this workflow, a key safety challenge is distinguishing truly unsupported recommendations from evidence-supported options that still require oncologist review because of incomplete information, poor ECOG performance status, or other clinical caveats. We introduce OpenMTB-Audit, an open-source benchmark of 500 synthetic non-small cell lung cancer cases spanning five adversarial error categories and four safety labels: Supported, Partially Supported, Unsupported, and Insufficient Information. Across eight large language model configurations, we identify pervasive over-refusal: all LLM configurations failed to retain the Partially Supported label in 83.3-100% of true Partially Supported cases, achieving high aggregate safety scores through label collapse rather than clinically calibrated reasoning. To address this limitation, we developed MTB-AuditAgent, a deterministic seven-module framework separating evidence verification, missing-information detection, safety classification, and abstention. It reduces over-refusal to 6.7% and achieves 91.2% accuracy (95% CI: 88.6-93.6%). A two-oncologist annotation study found disagreement concentrated at the boundary between information sufficiency and treatment optimization, underscoring the need to preserve clinically meaningful distinctions.
Artificial intelligence (AI) is increasingly embedded in precision oncology, shaping molecular classification, biomarker interpretation, treatment selection, toxicity prediction, trial matching, and disease monitoring—yet institutional governance has not kept pace with clinical adoption. An original cross-sectional s...
Yan Leyfman, A. Loaiza-Bonilla· AI in Precision Oncology· 0 citations
Together, these findings identify two complementary dimensions of open-ended decision support: coverage of clinically relevant content and coherent links among pathways, conditions and subsequent actions.
Dao-Yun Wang, Zhi-Cheng Huang, Hua-Yu Sun et al.· 0 citations
CHESTPHENOT is a compact 0.5-3B language model that jointly extracts finding labels, three-class status (present/absent/uncertain), and verbatim supporting evidence spans and demonstrates that locally deployable models can provide competitive and directly auditable radiology-report extraction without relying on externa...
Kai Yu, Chen-Yu Zhu, Zai-Fu Zhan et al.· 0 citations
This Viewpoint defines an AI agent as a feedback-driven system that maintains task state, selects among governed tools, observes results, and revises its plan under explicit safety constraints, and separates agents from multimodal foundation models, retrieval-augmented generation, and fixed workflow automation.
Liu-Yang Yang, Liyu Shan, Xiang-Mei Yao et al.· JMIR Cancer· 0 citations
OncoGenRAG is a research framework that combines a parameter-efficiently fine-tuned BioBERT classifier with an entity-aware retrieval system over a curated, multi-source oncology knowledge base and provides a transparent design for evidence retrieval and abstention.
Amaan Arif, J. V. dos Santos· bioRxiv· 0 citations
LLMs delivered promising results as assistive tools for RCA in radiation oncology, with the ability to generate relevant and accurate analyses aligned with expert expectations.
Yun-Tao Wang, M. De Ornelas, M. T. Studenski et al.· PLOS Digital Health· 0 citations
Assistant Professor Benjamin Lindquist studies how engineers deliberately injected randomness into early AI, giving rise to deep-learning models that sometimes hallucinate.