1. Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort.
- Author
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Shi, Zhuqing, Wei, Jun, Rifkin, Andrew S., Wang, Chi-Hsiung, Billings, Liana K., Woo, Jonathan S.H., Talamonti, Mark S., Vogel, Tilley Jenkins, Moore, Elena, Brockstein, Bruce E., Khandekar, Janardan D., Dunnenberger, Henry M., Hulick, Peter J., Duggan, David, Zheng, S. Lilly, Lee, Cheong Jun, Helfand, Brian T., Tafur, Alfonso J., and Xu, Jianfeng
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THROMBOSIS , *THROMBOEMBOLISM , *GENETIC mutation - Abstract
Cancer-associated thrombosis (CAT) is common and associated with mortality. We estimated CAT rate by cancer sites and inherited factors among cancer patients from the UK Biobank (N =70,406). The 12-month CAT rate after cancer diagnosis was 2.37% overall but varied considerably among cancer sites. Among the 10 cancer sites classified as 'high-risk' of CAT by the National Comprehensive Cancer Network guidelines, 6 had CAT rate <5%. In contrast, 5 cancer sites classified as 'average-risk' by the guidelines had CAT rate >5%. For inherited risk factors, both known mutation carriers in two genes (F5/F2) and polygenic score for venous thromboembolism (VTE) (PGS VTE) were independently associated with increased CAT risk. While F5/F2 identified 6% patients with high genetic-risk for CAT, adding PGS VTE identified 13 % patients at equivalent/higher genetic-risk to CAT than that of F5/F2 mutations. Findings from this large prospective study, if confirmed, provide critical data to update guidelines for CAT risk assessment. • Cancer-associated thrombosis (CAT) is common; its rate differs by cancer site and genetic factor. • CAT rates by cancer site and inherited factor were estimated in a large population-based cohort. • Cancer sites that are at increased risk for CAT differ considerably from current guidelines. • Both polygenic score and known mutations in F5 / F2 genes are associated with CAT risk. • Polygenic score and F5 / F2 gene mutations can identify 13% cancer patients at increased risk for CAT. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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