Osteosarcoma Explorer: A Data Commons With Clinical, Genomic, Protein, and Tissue Imaging Data for Osteosarcoma Research

Author:

Yang Donghan M.12ORCID,Zhou Qinbo1,Furman-Cline Lauren3,Cheng Xian1,Luo Danni1,Lai Hongyin14,Li Yueqi1,Jin Kevin W.1ORCID,Yao Bo1,Leavey Patrick J.23ORCID,Rakheja Dinesh5ORCID,Lo Tammy6,Hall David6ORCID,Barkauskas Donald A.67ORCID,Shulman David S.8,Janeway Katherine8ORCID,Khanna Chand9,Gorlick Richard10ORCID,Menzies Christopher11,Zhan Xiaowei12ORCID,Xiao Guanghua1212,Skapek Stephen X.23,Xu Lin12ORCID,Klesse Laura J.23ORCID,Crompton Brian D.813ORCID,Xie Yang1212ORCID

Affiliation:

1. Quantitative Biomedical Research Center, Peter O'Donnell Jr School of Public Health, The University of Texas Southwestern Medical Center, Dallas, TX

2. Simmons Comprehensive Cancer Center, The University of Texas Southwestern Medical Center, Dallas, TX

3. Department of Pediatrics, The University of Texas Southwestern Medical Center, Dallas, TX

4. Department of Biostatistics and Data Science, School of Public Health, University of Texas Health Science Center at Houston (UT Health), Houston, TX

5. Department of Pathology, The University of Texas Southwestern Medical Center, Dallas, TX

6. Children's Oncology Group Statistics and Data Center, Monrovia, CA

7. Department of Population and Public Health Sciences, Keck School of Medicine of the University of Southern California, Los Angeles, CA

8. Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA

9. Ethos Discovery, San Diego, CA

10. Division of Pediatrics, University of Texas MD Anderson Cancer Center, Houston, TX

11. Children's Medical Center, Dallas, TX

12. Department of Bioinformatics, The University of Texas Southwestern Medical Center, Dallas, TX

13. Broad Institute of Harvard and MIT, Cambridge, MA

Abstract

PURPOSE Osteosarcoma research advancement requires enhanced data integration across different modalities and sources. Current osteosarcoma research, encompassing clinical, genomic, protein, and tissue imaging data, is hindered by the siloed landscape of data generation and storage. MATERIALS AND METHODS Clinical, molecular profiling, and tissue imaging data for 573 patients with pediatric osteosarcoma were collected from four public and institutional sources. A common data model incorporating standardized terminology was created to facilitate the transformation, integration, and load of source data into a relational database. On the basis of this database, a data commons accompanied by a user-friendly web portal was developed, enabling various data exploration and analytics functions. RESULTS The Osteosarcoma Explorer (OSE) was released to the public in 2021. Leveraging a comprehensive and harmonized data set on the backend, the OSE offers a wide range of functions, including Cohort Discovery, Patient Dashboard, Image Visualization, and Online Analysis. Since its initial release, the OSE has experienced an increasing utilization by the osteosarcoma research community and provided solid, continuous user support. To our knowledge, the OSE is the largest (N = 573) and most comprehensive research data commons for pediatric osteosarcoma, a rare disease. This project demonstrates an effective framework for data integration and data commons development that can be readily applied to other projects sharing similar goals. CONCLUSION The OSE offers an online exploration and analysis platform for integrated clinical, molecular profiling, and tissue imaging data of osteosarcoma. Its underlying data model, database, and web framework support continuous expansion onto new data modalities and sources.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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