Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen

Jun 17, 2019·
Michael P. Menden
,
Dennis Wang
,
Mike J. Mason
,
Bence Szalai
,
Krishna C. Bulusu
,
Yuanfang Guan
,
Thomas Yu
,
Jaewoo Kang
,
Minji Jeon
,
Russ Wolfinger
,
Tin Nguyen
,
Mikhail Zaslavskiy
,
AstraZeneca-Sanger Drug Combination DREAM Consortium Including Feng GAO
,
In Sock Jang
,
Zara Ghazoui
,
Mehmet Eren Ahsen
,
Robert Vogel
,
Elias Chaibub Neto
,
Thea Norman
,
Eric K. Y. Tang
,
Mathew J. Garnett
,
Giovanni Y. Di Veroli
,
Stephen Fawell
,
Gustavo Stolovitzky
,
Justin Guinney
,
Jonathan R. Dry
,
Julio Saez-Rodriguez
· 0 min read
Abstract
The effectiveness of most cancer targeted therapies is short-lived. Tumors often develop resistance that might be overcome with drug combinations. However, the number of possible combinations is vast, necessitating data-driven approaches to find optimal patient-specific treatments. Here we report AstraZeneca’s large drug combination dataset, consisting of 11,576 experiments from 910 combinations across 85 molecularly characterized cancer cell lines, and results of a DREAM Challenge to evaluate computational strategies for predicting synergistic drug pairs and biomarkers. 160 teams participated to provide a comprehensive methodological development and benchmarking. Winning methods incorporate prior knowledge of drug-target interactions. Synergy is predicted with an accuracy matching biological replicates for >60% of combinations. However, 20% of drug combinations are poorly predicted by all methods. Genomic rationale for synergy predictions are identified, including ADAM17 inhibitor antagonism when combined with PIK3CB/D inhibition contrasting to synergy when combined with other PI3K-pathway inhibitors in PIK3CA mutant cells.
Type
Publication
Nature Communications
publication