Evidence map›Paper›PMID 41646323›Full record

ArticleResearch square2026

PAIRWISE: Deep Learning-based Prediction of Effective Personalized Drug Combinations in Cancer.

Chengqi Xu, Ilkay Us, Jake Cohen-Setton, Marta Milo, Ben Sidders, Jude Fitzgibbon, Ari M Melnick, Heng Pan, Krishna C Bulusu, Olivier Elemento

Abstract readPreprint
In one paragraph

Article in Research square, 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.

Chengqi XuEnglander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.ORCID https://orcid.org/0000-0003-3361-8117
Ilkay UsEnglander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.
Jake Cohen-SettonOncology Data Science, AstraZeneca, Cambridge, UK.
Marta MiloOncology Data Science, AstraZeneca, Cambridge, UK.
Ben SiddersOncology Data Science, AstraZeneca, Cambridge, UK.
Jude FitzgibbonHematology R&D, AstraZeneca, Waltham, MA, USA.ORCID https://orcid.org/0000-0002-9069-1866
Ari M MelnickDivision of Hematology and Oncology, Department of Medicine and Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.ORCID https://orcid.org/0000-0002-8074-2287
Heng PanState Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-5407-5687
Krishna C BulusuOncology Data Science, AstraZeneca, Cambridge, UK.
Olivier ElementoEnglander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.ORCID https://orcid.org/0000-0002-8061-9617

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
Project 3: Targeting PRMT5 in Mantle Cell LymphomaP01CA214274 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BALLMAN, KARLA V. · 2018 to 2022
$8.9M
The identification and validation of mechanisms and biomarkers for relapse in diffuse large B-cell lymphoma (Administrative Supplement)R01CA194547 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ELEMENTO, OLIVIER, TAM, WAYNE · 2015 to 2019
$2.6M
Intercepting progression from pre-invasive to invasive lung adenocarcinomaUG3CA244697 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ALTORKI, NASSER KHALED, BORCZUK, ALAIN C · 2019 to 2021
$2.1M
NCATS NIH HHS UL1 TR001873NCATS NIH HHS UL1 TR002384NCI NIH HHS P01 CA214274NCI NIH HHS R01 CA194547NCI NIH HHS UG3 CA244697
6 · The paper itself

Abstract

Combination therapies offer promise for improving cancer treatment efficacy and preventing recurrence. Preclinical screening strategies can prioritize synergistic drug combinations. However, identifying optimal drug combinations tailored to specific cancer subtypes and individual patients is extremely challenging due to the vast number of possible combinations and tumor heterogeneity. To address this gap, we combined deep learning with transfer learning to incorporate prior scientific knowledge and predicted drug synergy based on tumor-specific transcriptome profiles. PAIRWISE explicitly modeled synergistic effects of drug combinations in cancer cell lines or individual tumor samples based on drug chemical structures, drug targets, and transcriptomes of inferred samples. Of note, PAIRWISE outperformed competing models with an AUROC (the area under the receiver operating characteristic curve) of 0.847 on held-out cancer cell lines. Moreover, when applied to an independent dataset of combinations with Bruton Tyrosine Kinase inhibitors (BTKi) in Diffuse Large B Cell Lymphoma (DLBCL) cell lines, PAIRWISE accurately predicted synergistic drug combinations with an AUROC of 0.720. To further confirm the robustness of PAIRWISE predictions, we selected 30 approved or investigational agents for DLBCL treatment and validated their synergy with BTKi across eight non-Hodgkin lymphoma cell lines. The synergistic predictions of PAIRWISE showed strong concordance with

Identifiers

PMID41646323
PMCPMC12869695

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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.