Evidence map›Paper›PMID 42465958›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Assessment of Zero-Shot Large Language Model (LLM) Assisted Clinical Trial Matching Processes: A Metastatic Cancer Use Case.

Yingjie Weng, Himani Yalamaddi, Danning Fu, Ankita Mishra, Bryan J Bunning, Andrew B Martin, Jessica Hope, Vivek Charu, Allison Kurian, Manisha Desai

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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
–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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

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

10 authors.

Yingjie WengQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Himani YalamaddiQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Danning FuQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Ankita MishraQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Bryan J BunningQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Andrew B MartinQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Jessica HopeQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Vivek CharuQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.
Allison KurianStanford University School of Medicine, Stanford, CA.
Manisha DesaiQuantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA.

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI MICHAEL KENNEY · 2007 to 2026
$71.4M
Stanford Center for Clinical & Translational Education and Research (Spectrum)UL1TR003142 · NCATS · STANFORD UNIVERSITY · PI O'HARA, RUTH M · 2019 to 2023
$45.0M
NCATS NIH HHS UL1 TR003142NCI NIH HHS P30 CA124435
6 · The paper itself

Abstract

Introduction: For oncology patients with limited treatment options, clinical trials may be a critical lifesaving pathway. Identifying relevant trials, however, is a time-consuming and difficult task. Several patient-trial matching processes incorporating large language models (LLMs) have been proposed to alleviate the burden on patients and oncologists. We aim to explore the benefits and practical challenges of zero-shot LLM-assisted trial matching processes by analyzing the results for a single pancreatic cancer patient. Materials and Methods: The results of a simple zero-shot LLM-assisted clinical trial matching process for our patient were compared to those of a "human benchmark," which was developed manually by two of the authors interfacing directly with ClinicalTrials.gov. Performance metrics - sensitivity, specificity, precision, and accuracy - were calculated. In addition, a qualitative content analysis (QCA) of LLM reasoning text was done to identify patterns in "errors," which we define as a human-LLM discrepancy in final patient eligibility. Implications and severity of errors are discussed. Results: The zero-shot LLM-assisted process returned potential trials with a sensitivity, specificity, and precision of 81.1%, 89.3%, and 86.5% respectively compared to the human benchmark. Qualitative error analyses revealed that about 73% of errors could potentially be alleviated with improved prompting and information access. Overall performance seemed comparable to that of human reviewers. Conclusion: The results from this preliminary real-world case study provide additional evidence to the literature in support of the integration of LLMs in clinical trial matching to provide benefit to patients with metastatic cancer with limited options.

Indexed as

cancer careclinical trial matchinglarge language models

Identifiers

PMID42465958
PMCPMC13370548

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Registered trials

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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.