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Opportunities and Challenges for Analyzing Cancer Data at the Inter- and Intra-Institutional Levels.

Publication ,  Journal Article
Wu, J; Bryan, J; Rubinstein, SM; Wang, L; Lenoue-Newton, M; Zuhour, R; Levy, M; Micheel, C; Xu, Y; Bhavnani, SK; Mackey, L; Warner, JL
Published in: JCO precision oncology
January 2020

Our goal was to identify the opportunities and challenges in analyzing data from the American Association of Cancer Research Project Genomics Evidence Neoplasia Information Exchange (GENIE), a multi-institutional database derived from clinically driven genomic testing, at both the inter- and the intra-institutional level. Inter-institutionally, we identified genotypic differences between primary and metastatic tumors across the 3 most represented cancers in GENIE. Intra-institutionally, we analyzed the clinical characteristics of the Vanderbilt-Ingram Cancer Center (VICC) subset of GENIE to inform the interpretation of GENIE as a whole.We performed overall cohort matching on the basis of age, ethnicity, and sex of 13,208 patients stratified by cancer type (breast, colon, or lung) and sample site (primary or metastatic). We then determined whether detected variants, at the gene level, were associated with primary or metastatic tumors. We extracted clinical data for the VICC subset from VICC's clinical data warehouse. Treatment exposures were mapped to a 13-class schema derived from the HemOnc ontology.Across 756 genes, there were significant differences in all cancer types. In breast cancer, ESR1 variants were over-represented in metastatic samples (odds ratio, 5.91; q < 10-6). TP53 mutations were over-represented in metastatic samples across all cancers. VICC had a significantly different cancer type distribution than that of GENIE but patients were well matched with respect to age, sex, and sample type. Treatment data from VICC was used for a bipartite network analysis, demonstrating clusters with a mix of histologies and others being more histology specific.This article demonstrates the feasibility of deriving meaningful insights from GENIE at the inter- and intra-institutional level and illuminates the opportunities and challenges of the data GENIE contains. The results should help guide future development of GENIE, with the goal of fully realizing its potential for accelerating precision medicine.

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Published In

JCO precision oncology

DOI

EISSN

2473-4284

ISSN

2473-4284

Publication Date

January 2020

Volume

4

Start / End Page

PO.19.00394

Related Subject Headings

  • 3211 Oncology and carcinogenesis
 

Citation

APA
Chicago
ICMJE
MLA
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Wu, J., Bryan, J., Rubinstein, S. M., Wang, L., Lenoue-Newton, M., Zuhour, R., … Warner, J. L. (2020). Opportunities and Challenges for Analyzing Cancer Data at the Inter- and Intra-Institutional Levels. JCO Precision Oncology, 4, PO.19.00394. https://doi.org/10.1200/po.19.00394
Wu, Julie, Jordan Bryan, Samuel M. Rubinstein, Lucy Wang, Michele Lenoue-Newton, Raed Zuhour, Mia Levy, et al. “Opportunities and Challenges for Analyzing Cancer Data at the Inter- and Intra-Institutional Levels.JCO Precision Oncology 4 (January 2020): PO.19.00394. https://doi.org/10.1200/po.19.00394.
Wu J, Bryan J, Rubinstein SM, Wang L, Lenoue-Newton M, Zuhour R, et al. Opportunities and Challenges for Analyzing Cancer Data at the Inter- and Intra-Institutional Levels. JCO precision oncology. 2020 Jan;4:PO.19.00394.
Wu, Julie, et al. “Opportunities and Challenges for Analyzing Cancer Data at the Inter- and Intra-Institutional Levels.JCO Precision Oncology, vol. 4, Jan. 2020, p. PO.19.00394. Epmc, doi:10.1200/po.19.00394.
Wu J, Bryan J, Rubinstein SM, Wang L, Lenoue-Newton M, Zuhour R, Levy M, Micheel C, Xu Y, Bhavnani SK, Mackey L, Warner JL. Opportunities and Challenges for Analyzing Cancer Data at the Inter- and Intra-Institutional Levels. JCO precision oncology. 2020 Jan;4:PO.19.00394.

Published In

JCO precision oncology

DOI

EISSN

2473-4284

ISSN

2473-4284

Publication Date

January 2020

Volume

4

Start / End Page

PO.19.00394

Related Subject Headings

  • 3211 Oncology and carcinogenesis