Performance of large language models for extracting clinical data from breast cancer pathology reports: a systematic review

Breast cancer pathology reports contain critical clinical information, yet manual extraction of structured data remains resource-intensive and error-prone. Large language models (LLMs) offer promising automated approaches, but no systematic synthesis examines their performance specifically for breast cancer pathology report processing. Following PRISMA guidelines, we searched seven databases from inception to December 2025, with two reviewers independently screening studies and extracting data. Methodological quality was assessed using PROBAST + AI and reporting completeness using TRIPOD + AI. Nine studies met inclusion criteria, evaluating over 30 distinct LLM architectures across datasets totaling approximately 14,161 reports. Best-performing models achieved study-specific accuracy ranging from 87.7% to 97.4%, though figures are not directly comparable across studies due to differences in task formulation, target data elements, and evaluation metrics. PROBAST + AI assessment found 55.6% of studies at low concern/risk across all domains, with the Outcome domain showing greatest variability. TRIPOD + AI revealed gaps in fairness reporting, open science practices, and patient/public involvement. LLMs demonstrate promising performance approaching human-level accuracy, but methodological quality varies, with key concerns regarding reference standard development, limited external validation, and inadequate fairness reporting.

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Publication Details

Journal
npj Digital Medicine
Published
2026-05-22
DOI
https://doi.org/10.1038/s41746-026-02789-x
Primary Topic
AI in cancer detection
Type
article
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article

Performance of large language models for extracting clinical data from breast cancer pathology reports: a systematic review

Pei Yi Sin, Vahul Sundar, Ern Yu Tan, Ravi Shankar et al.
npj Digital Medicine
AI in cancer detection
article

Performance of large language models for extracting clinical data from breast cancer pathology reports: a systematic review

Pei Yi Sin, Vahul Sundar, Ern Yu Tan, Ravi Shankar, Ziyu Goh
article en

Abstract

Breast cancer pathology reports contain critical clinical information, yet manual extraction of structured data remains resource-intensive and error-prone. Large language models (LLMs) offer promising automated approaches, but no systematic synthesis examines their performance specifically for breast cancer pathology report processing. Following PRISMA guidelines, we searched seven databases from inception to December 2025, with two reviewers independently screening studies and extracting data. Methodological quality was assessed using PROBAST + AI and reporting completeness using TRIPOD + AI. Nine studies met inclusion criteria, evaluating over 30 distinct LLM architectures across datasets totaling approximately 14,161 reports. Best-performing models achieved study-specific accuracy ranging from 87.7% to 97.4%, though figures are not directly comparable across studies due to differences in task formulation, target data elements, and evaluation metrics. PROBAST + AI assessment found 55.6% of studies at low concern/risk across all domains, with the Outcome domain showing greatest variability. TRIPOD + AI revealed gaps in fairness reporting, open science practices, and patient/public involvement. LLMs demonstrate promising performance approaching human-level accuracy, but methodological quality varies, with key concerns regarding reference standard development, limited external validation, and inadequate fairness reporting.

npj Digital Medicine
Agency for Science, Technology and Research (SG), National University of Singapore (SG), Nanyang Technological University (SG), Tan Tock Seng Hospital (SG), Institute of Molecular and Cell Biology (SG)
Openalex Percentile: Top 4%
AI in cancer detection
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Performance of large language models for extracting clinical data from breast cancer pathology reports: a systematic review — Pei Yi Sin, Vahul Sundar, et al. · npj Digital Medicine (2026) | TGRS Research Map | TGRS