Cardiovascular disease risk among long-term testicular cancer survivors following contemporary cisplatin-based chemotherapy

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Authors: Sarah L. Kerns, Paul C. Dinh, Patrick O. Monahan, Chunkit Fung, Howard D. Sesso, Darren Richard Feldman, Robert J. Hamilton, Phillip Pierazio, Robert Anthony Huddart, Christian Kollmannsberger, Neil E. Martin, Lawrence H. Einhorn
+1 more Lois B. Travis
Cited by: 0

Abstract

Testicular cancer survivors (TCS) experience excess cardiovascular disease (CVD) incidence and mortality. To address the urgent need for new risk prediction tools, we evaluated the AHA's 2024 PREVENT-equation among 1,759 TC survivors (TCS; median baseline age = 37 years). Baseline median 10- and 30-year CVD risks were 1.3% and 9.1%. Among evaluated survivors with follow-up (N = 737; median age = 45), each 5% increase in 10-year PREVENT risk conferred 2.94-fold odds (95%CI = 1.99-4.35, P < .001) of incident CVD. Those with 10-year PREVENT absolute risk defined as intermediate-high (≥7.5% per AHA) had 12.11-fold higher odds (P < .001). Associations were strongest after four cycles of etoposide/cisplatin (EPX4) (OR = 4.93, P < .001), possibly driven by lower eGFR and slightly older age (P < .001 each), and among TCS without vigorous baseline physical-activity (OR = 4.25, P < .001). EPX4 patients were among those less engaged in activity (P = .005). PREVENT equations, utilizing routine measures, can identify high-risk TCS, highlighting physical-activity as a key modifiable factor for early intervention.

Fields of Study & Subjects

Chemotherapy-induced cardiotoxicity and mitigation Cancer survivorship and care Testicular diseases and treatments

Publication details

Journal / source
JNCI Journal of the National Cancer Institute
Publication date
6 February 2026
Language
EN