Evidence map›Paper›PMID 42422657›Full record

ArticleCureus2026

Large Language Model Morphology-to-Genotype Inference for Microsatellite Instability From Colorectal Carcinoma Histopathology Reports.

Mimna V M

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Mimna V MPathology, All India Institute of Medical Sciences, Gorakhpur, Gorakhpur, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microsatellite instability (MSI) is an important prognostic and predictive biomarker in colorectal carcinoma and is associated with several characteristic histomorphological features. While large language models (LLMs) have been investigated for structured data extraction from histopathology reports, their ability to infer molecular genotype from text-based morphologic descriptions remains underexplored. This study evaluated structured data extraction, MSI prediction performance, confidence behavior, and biological reasoning quality of two LLMs using colorectal carcinoma pathology reports with The Cancer Genome Atlas (TCGA)-assigned MSI status as the reference standard. Fifty colorectal carcinoma reports, including 25 MSI-high (MSI-H) and 25 microsatellite-stable (MSS), from TCGA database were stratified by morphologic signal strength. ChatGPT 5.2 (OpenAI, San Francisco, CA) and Gemini 3 (Google, Mountain View, CA) were given an identical zero-shot prompt to extract 17 histopathologic variables across structural, staging, invasion, and MSI-associated morphologic categories, predict MSI status with confidence scores, and provide biological justification. Both models demonstrated high extraction accuracy for structural variables (85.0-88.5%) but substantially lower performance for MSI-associated morphologic variables (ChatGPT 5.2: 39.4%; Gemini 3: 43.9%), with mucinous differentiation showing the highest omission rate and signet ring cell morphology the lowest extraction accuracy. Overall, MSI prediction accuracy was 64.0% for Gemini 3 and 16.0% for ChatGPT 5.2. Among committed predictions, ChatGPT 5.2 demonstrated perfect specificity and positive predictive value, whereas Gemini 3 showed a morphologic signal-dependent accuracy gradient and a substantially higher rate of high-confidence incorrect predictions (20.0% versus 2.0%). General-purpose LLMs demonstrated variable ability to recognize MSI-associated histomorphologic descriptors, with systematic failures in extraction directly limiting downstream genotype inference.

Indexed as

colorectal carcinomadigital pathologyhistopathology reportslarge language modelsmedical artificial intelligencemicrosatellite instability

Identifiers

PMID42422657
PMCPMC13344910

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.