Evidence map›Paper›PMID 41756848›Full record

ArticlebioRxiv : the preprint server for biology2026

A Pan-Cancer Ex Vivo Drug Screen Atlas for Functional Precision Oncology.

Karl Pichotta, Jessica B White, Jeffrey F Quinn, Anneliese Markus, Christopher Tosh, Antoine De Mathelin, Erin Coyne, Feiyang Huang, Wesley Tansey

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

9 authors.

Karl PichottaComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Jessica B WhiteComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Jeffrey F QuinnComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Anneliese MarkusJacobs School of Medicine and Biomedical Sciences, SUNY University at Buffalo, Buffalo, NY 14203, United States.
Christopher ToshComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Antoine De MathelinComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Erin CoyneDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, IN 46556, United States.
Feiyang HuangComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.
Wesley TanseyComputational Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, United States.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
The Center for Tumor-Immune Systems Biology at MSKCCU54CA274492 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Alexander Y Rudensky · 2022 to 2026
$16.3M
Probabilistic Multiscale Modeling of the Tumor MicroenvironmentR37CA271186 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Wesley Tansey · 2023 to 2026
$2.7M
NCI NIH HHS P30 CA008748NCI NIH HHS R37 CA271186NCI NIH HHS U54 CA274492
6 · The paper itself

Abstract

Compared to immortalized cell lines, patient-derived organoids and other ex vivo models have been shown to better recapitulate patient responses to therapy. High cost and technical complexity have prevented the creation of pan-cancer ex vivo datasets, limiting comprehensive analyses and predictive modeling for ex vivo drug response. We present the Pan-PreClinical (PPC) project: a drug screen atlas of 2.1M experiments across 1,982 ex vivo samples and 3,100 drugs spanning 134 cancer indications tested across 26 studies. We develop a contrastive Bayesian model to harmonize across studies, identifying 303 tissue-specific drug sensitivities and demonstrating drug sensitivities are predictive of clinically-relevant molecular profiles. Integrating established cell line databases reveals systematic biases across 55 cancer subtypes, with cell line screens favoring drugs targeting highly proliferative cells and undervaluing cell-cell communication targets. We leverage PPC to establish an ex vivo foundation model and computational platform for scalable ex vivo cancer biology and predictive oncology.

Identifiers

PMID41756848
PMCPMC12934811

What OpenQuestion holds

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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.