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Published on: July 25, 2020
ClinicalOmicsDB: exploring molecular associations of oncology drug responses in clinical trials
Chang In Moon1,2, John Michael Elizarraras1,2, Jonathan Thomas Lei1,2
1Lester and Sue Smith Breast Center and Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Abstract:
Matching patients to optimal treatment is challenging, in part due to the limited availability of real-world clinical datasets for predictive biomarker identification. The growing integration of omics profiling into clinical trials presents a new opportunity to tackle this challenge. Here, we introduce ClinicalOmicsDB, a web application for exploring molecular associations of oncology drug responses in clinical trials. This database includes transcriptomic data from 40 clinical trial studies, with 5913 patients spanning 11 cancer types. These studies include 67 treatment arms with a variety of chemotherapy, targeted therapy and immunotherapy drugs, and their combinations, which we organize based on an established ontology for easier navigation. The web application provides users with three options to explore molecular associations of oncology drug responses, focusing on studies, treatments or genes, respectively. Gene set analysis further connects treatment response to pathway activity and tumor microenvironment attributes. The user-friendly web interface of ClinicalOmicsDB streamlines interactive analysis. A Rust-based backend speeds up response time, and application programming interfaces and an R package enable programmatic access. We use three case studies to demonstrate the utility of this resource in human cancer studies. ClinicalOmicsDB is freely available at http://trials.linkedomics.org/.
Insights
ClinicalOmicsDB is a new web tool linking omics data from clinical trials to cancer drug responses. It helps identify predictive biomarkers for personalized oncology treatments.
Area of Science:
- Computational Biology
- Bioinformatics
- Oncology
Background:
- Predictive biomarker identification for optimal cancer treatment is hindered by limited real-world clinical data.
- The integration of omics profiling in clinical trials offers a novel approach to address this challenge.
Purpose of the Study:
- To introduce ClinicalOmicsDB, a web application designed for exploring molecular associations with oncology drug responses within clinical trial data.
- To facilitate the identification of predictive biomarkers for personalized cancer therapy.
Main Methods:
- Compiled transcriptomic data from 40 clinical trials (5913 patients, 11 cancer types, 67 treatment arms) including various drug types and combinations.
- Organized data using an established ontology for intuitive navigation.
- Developed a user-friendly web interface with options to explore associations by study, treatment, or gene.
- Integrated gene set analysis for pathway and tumor microenvironment attributes.
- Implemented a Rust-based backend for performance and provided API/R package for programmatic access.
Main Results:
- ClinicalOmicsDB provides a comprehensive resource linking molecular data to drug response across diverse cancer types and treatments.
- The platform enables interactive exploration of gene expression patterns associated with treatment efficacy.
- Case studies demonstrate the utility of ClinicalOmicsDB in uncovering potential predictive biomarkers for human cancer studies.
Conclusions:
- ClinicalOmicsDB serves as a valuable, freely accessible resource for researchers in oncology and bioinformatics.
- The tool streamlines the analysis of complex omics data from clinical trials to advance personalized medicine.
- Facilitates the discovery of novel molecular associations to improve patient treatment selection.
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