Evidence map›Paper›PMID 40778147›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Implementing a context-augmented large language model to guide precision cancer medicine.

Hyeji Jun, Yutaro Tanaka, Shreya Johri, Filipe Lf Carvalho, Alexander C Jordan, Chris Labaki, Matthew Nagy, Tess A O'Meara, Theodora Pappa, Erica Maria Pimenta and 6 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

5 · Who and what money

Authors and funding

16 authors.

Hyeji JunDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.ORCID 0000-0002-5796-7103
Yutaro TanakaBroad Institute of Harvard and MIT, Cambridge, MA 02142, USA.ORCID 0009-0004-1060-7065
Shreya JohriDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Filipe Lf CarvalhoDepartment of Urology, Brigham and Women's Hospital, Boston, MA 02115, USA.ORCID 0000-0003-2378-6512
Alexander C JordanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Chris LabakiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Matthew NagyBroad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Tess A O'MearaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Theodora PappaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Erica Maria PimentaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Eddy SaadDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
David D YangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.ORCID 0000-0002-5146-218X
Riaz GillaniBroad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Alok K TewariDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.ORCID 0000-0003-2617-7499
Brendan ReardonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.ORCID 0000-0002-1716-5720
Eliezer Van AllenDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.ORCID 0000-0002-0201-4444

Funding

Molecular Determinants of Response and Resistance to EZH2 and PARP inhibition in Prostate CancerP50CA272390 · NCI · DANA-FARBER CANCER INST · PI Steven P. Balk, Himisha Beltran · 2023 to 2026
$12.0M
NCI NIH HHS P50 CA272390
6 · The paper itself

Abstract

The rapid expansion of molecularly informed therapies in oncology, coupled with evolving regulatory FDA approvals, poses a challenge for oncologists seeking to integrate precision cancer medicine into patient care. Large Language Models (LLMs) have demonstrated potential for clinical applications, but their reliance on general knowledge limits their ability to provide up-to-date and niche treatment recommendations. To address this challenge, we developed a RAG-LLM workflow augmented with Molecular Oncology Almanac (MOAlmanac), a curated precision oncology knowledge resource, and evaluated this approach relative to alternative frameworks (i.e. LLM-only) in making biomarker-driven treatment recommendations using both unstructured and structured data. We evaluated performance across 234 therapy-biomarker relationships. Finally, we assessed real-world applicability of the workflow by testing it on actual queries from practicing oncologists. While LLM-only achieved 62-75% accuracy in biomarker-driven treatment recommendations, RAG-LLM achieved 79-91% accuracy with an unstructured database and 94-95% accuracy with a structured database. In addition to accuracy, structured context augmentation significantly increased precision (49% to 80%) and F1-score (57% to 84%) compared to unstructured data augmentation. In queries provided by practicing oncologists, RAG-LLM achieved 81-90% accuracy. These findings demonstrate that the RAG-LLM framework effectively delivers precise and reliable FDA-approved precision oncology therapy recommendations grounded in individualized clinical data, and highlight the importance of integrating a well-curated, structured knowledge base in this process. While our RAG-LLM approach significantly improved accuracy compared to standard LLMs, further efforts will enhance the generation of reliable responses for ambiguous or unsupported clinical scenarios.

Identifiers

PMID40778147
PMCPMC12330419

What OpenQuestion holds

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LicenceCC BY-NC
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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.