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PAIRWISE: Deep Learning-based Prediction of Effective Personalized Drug Combinations in Cancer
Olivier Elemento1,2,3, Chengqi Xu1, Ilkay Us4
1Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.
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 in vitro screening results. These findings highlight PAIRWISE's potential as a powerful in silico tool to prioritize candidate personalized drug combinations for further experimental validation.
Insights
This study introduces PAIRWISE, a novel computational model for predicting synergistic drug combinations in cancer. PAIRWISE accurately identifies effective personalized cancer therapies, advancing precision oncology.
Area of Science:
- Computational biology
- Oncology
- Pharmacology
Background:
- Combination therapies are crucial for enhancing cancer treatment efficacy and preventing recurrence.
- Identifying optimal drug combinations is challenging due to numerous possibilities and tumor heterogeneity.
- Preclinical screening can prioritize synergistic drug combinations, but personalized approaches are needed.
Purpose of the Study:
- To develop a computational model, PAIRWISE, for predicting synergistic drug combinations in cancer.
- To address the challenge of identifying personalized drug combinations tailored to specific cancer subtypes and patients.
- To accelerate the development of precision oncology through effective nomination of drug combinations.
Main Methods:
- Developed PAIRWISE, a model explicitly designed to predict synergistic effects of drug combinations.
- Applied PAIRWISE to held-out cancer cell lines and an independent dataset of Diffuse Large B Cell Lymphoma (DLBCL) treated with Bruton Tyrosine Kinase (BTK) inhibitors.
- Validated predictions using high-throughput screening (HTS) of approved or investigational agents for DLBCL.
Main Results:
- PAIRWISE demonstrated superior performance compared to competing models, achieving an AUROC of 0.847 on cancer cell lines.
- The model accurately predicted synergistic combinations in DLBCL with an AUROC of 0.720.
- PAIRWISE showed strong concordance with in vitro screening results, validating its predictive capability.
Conclusions:
- PAIRWISE effectively models synergistic drug effects and nominates personalized drug combinations for cancer treatment.
- The model shows significant potential for accelerating precision oncology development.
- This approach can guide the selection of effective combination therapies for individual patients.
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