Evidence map›Paper›PMID 39763776›Full record

ArticlebioRxiv : the preprint server for biology2024

A precision oncology-focused deep learning framework for personalized selection of cancer therapy.

Casey Sederman, Chieh-Hsiang Yang, Emilio Cortes-Sanchez, Tony Di Sera, Xiaomeng Huang, Sandra D Scherer, Ling Zhao, Zhengtao Chu, Eliza R White, Aaron Atkinson and 7 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

17 authors.

Casey SedermanEccles Institute of Human Genetics, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0001-5999-7675
Chieh-Hsiang YangHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Emilio Cortes-SanchezHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Tony Di SeraEccles Institute of Human Genetics, University of Utah, Salt Lake City, Utah, USA.
Xiaomeng HuangEccles Institute of Human Genetics, University of Utah, Salt Lake City, Utah, USA.
Sandra D SchererHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Ling ZhaoHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Zhengtao ChuHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Eliza R WhiteHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Aaron AtkinsonHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Jadon WagstaffHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Katherine E VarleyHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Michael T LewisDepartments of Molecular and Cellular Biology and Radiology. Lester and Sue Smith Breast Center. Dan L Duncan Comprehensive Cancer Center. Baylor College of Medicine, Houston, Texas, USA.
Yi QiaoDepartment of Biomedical Informatics, School of Medicine, University of Utah, Salt Lake City, UT, USA.
Bryan E WelmHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Alana L WelmHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Gabor T MarthEccles Institute of Human Genetics, University of Utah, Salt Lake City, Utah, USA.

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Suzanne AW Fuqua · 2007 to 2026
$73.9M
UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Tolinapant efficacy in a subset of triple negative breast cancersU54CA224076 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Alana L. Welm · 2017 to 2026
$13.5M
Longitudinal models of breast cancer for studying mechanisms of therapy response and resistanceU01CA217617 · NCI · UNIVERSITY OF UTAH · PI MARTH, GABOR T, VARLEY, KATHERINE ELENA · 2018 to 2022
$4.2M
From genomics to natural language processing: A protected environment for research computing in the health scienceS10OD021644 · OD · UNIVERSITY OF UTAH · PI CHEATHAM, THOMAS E. · 2017 to 2017
$494k
NCI NIH HHS P30 CA042014NCI NIH HHS P30 CA125123NCI NIH HHS U01 CA217617NCI NIH HHS U54 CA224076NIH HHS S10 OD021644
6 · The paper itself

Abstract

Precision oncology matches tumors to targeted therapies based on the presence of actionable molecular alterations. However, most tumors lack actionable alterations, restricting treatment options to cytotoxic chemotherapies for which few data-driven prioritization strategies currently exist. Here, we report an integrated computational/experimental treatment selection approach applicable for both chemotherapies and targeted agents irrespective of actionable alterations. We generated functional drug response data on a large collection of patient-derived tumor models and used it to train ScreenDL, a novel deep learning-based cancer drug response prediction model. ScreenDL leverages the combination of tumor omic and functional drug screening data to predict the most efficacious treatments. We show that ScreenDL accurately predicts response to drugs with diverse mechanisms, outperforming existing methods and approved biomarkers. In our preclinical study, this approach achieved superior clinical benefit and objective response rates in breast cancer patient-derived xenografts, suggesting that testing ScreenDL in clinical trials may be warranted.

Identifiers

PMID39763776
PMCPMC11702554

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.