- Menden, Michael P;
- Wang, Dennis;
- Mason, Mike J;
- Szalai, Bence;
- Bulusu, Krishna C;
- Guan, Yuanfang;
- Yu, Thomas;
- Kang, Jaewoo;
- Jeon, Minji;
- Wolfinger, Russ;
- Nguyen, Tin;
- Zaslavskiy, Mikhail;
- Jang, In Sock;
- Ghazoui, Zara;
- Ahsen, Mehmet Eren;
- Vogel, Robert;
- Neto, Elias Chaibub;
- Norman, Thea;
- Tang, Eric KY;
- Garnett, Mathew J;
- Veroli, Giovanni Y Di;
- Fawell, Stephen;
- Stolovitzky, Gustavo;
- Guinney, Justin;
- Dry, Jonathan R;
- Saez-Rodriguez, Julio
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.