Evidence map›Paper›PMID 40523223›Full record

ArticleJCO clinical cancer informatics2025

Reliability of Large Language Model Knowledge Across Brand and Generic Cancer Drug Names.

Jack Gallifant, Shan Chen, Sandeep K Jain, Pedro Moreira, Umit Topaloglu, Hugo J W L Aerts, Jeremy L Warner, William G La Cava, Danielle S Bitterman

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

9 authors.

Jack GallifantArtificial Intelligence in Medicine (AIM) Program, Mass General Brigham, Harvard Medical School, Boston, MA.ORCID 0000-0003-1306-2334
Shan ChenArtificial Intelligence in Medicine (AIM) Program, Mass General Brigham, Harvard Medical School, Boston, MA.ORCID 0000-0001-7999-7410
Sandeep K JainCenter for Clinical Cancer Informatics and Data Science, Legorreta Cancer Center, Brown University, Providence, RI.ORCID 0000-0003-2455-2494
Pedro MoreiraUniversitat Pompeu Fabra, Barcelona, Spain.
Umit TopalogluInformatics and Data Science Program, National Cancer Institute, Rockville, MD.ORCID 0000-0002-3241-8773
Hugo J W L AertsArtificial Intelligence in Medicine (AIM) Program, Mass General Brigham, Harvard Medical School, Boston, MA.ORCID 0000-0002-2122-2003
Jeremy L WarnerCenter for Clinical Cancer Informatics and Data Science, Legorreta Cancer Center, Brown University, Providence, RI.
William G La CavaComputational Health Informatics Program, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Danielle S BittermanArtificial Intelligence in Medicine (AIM) Program, Mass General Brigham, Harvard Medical School, Boston, MA.ORCID 0000-0003-0345-2232

Funding

Shared Resource Core 2: Clinical Artificial Intelligence CoreU54CA274516 · NCI · DANA-FARBER CANCER INST · PI Ross I. Berbeco · 2023 to 2026
$8.1M
Enhancing the HemOnc Knowledgebase of Chemotherapy Drugs and RegimensU24CA265879 · NCI · RHODE ISLAND HOSPITAL · PI Jeremy L Warner · 2022 to 2026
$3.4M
Informatics strategies to improve immune-related adverse event detection in cancer patientsR01CA294033 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Hugo Aerts · 2024 to 2026
$1.3M
NCI NIH HHS R01 CA294033NCI NIH HHS U24 CA265879NCI NIH HHS U54 CA274516
6 · The paper itself

Abstract

purposeTo evaluate the performance and consistency of large language models (LLMs) across brand and generic oncology drug names in various clinical tasks, addressing concerns about potential fluctuations in LLM performance because of subtle phrasing differences that could affect patient care.

methodsThis study evaluated three LLMs (GPT-3.5-turbo-0125, GPT-4-turbo, and GPT-4o) using drug names from HemOnc ontology. The assessment included 367 generic-to-brand and 2,516 brand-to-generic pairs, 1,000 drug-drug interaction (DDI) synthetic patient cases, and 2,438 immune-related adverse event (irAE) cases. LLMs were tested on drug name recognition, word association, DDI (DDI) detection, and irAE diagnosis using both brand and generic drug names.

resultsLLMs demonstrated high accuracy in matching brand and generic names (GPT-4o: 97.38% for brand, 94.71% for generic,

conclusionDespite high proficiency in name-matching, LLMs exhibit inconsistencies when processing brand versus generic drug names in more complex tasks. These findings highlight the need for increased awareness, improved robustness assessment methods, and the development of more consistent systems for handling nomenclature variations in clinical applications of LLMs.

Indexed as

Antineoplastic AgentsDrugs, GenericLanguageNeoplasmsTerminology as TopicDrug InteractionsHumansLarge Language ModelsReproducibility of ResultsAntineoplastic AgentsDrugs, Generic

Identifiers

PMID40523223
PMCPMC13502066

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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.