ArticleCardiovascular toxicology2026
Clinical Characteristics and Outcomes of Heart Failure with Preserved Ejection Fraction Versus Reduced Ejection Fraction in Patients Receiving Anticancer Drugs.
Article in Cardiovascular toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
This study aimed to compare prevalence, clinical features, and outcomes between patients with heart failure (HF) with preserved ejection fraction (HFpEF) and those with reduced ejection fraction (HFrEF) who received anticancer drugs. This single-center, retrospective study included 126 patients who developed new-onset HF or worsening HF after starting anticancer drug treatment between April 2018 and December 2023. HFrEF was defined as HF symptoms and signs with left ventricular ejection fraction (LVEF) < 50%, and HFpEF as LVEF ≥ 50%. Among the cohort, 49 patients (39%) had HF with New York Heart Association functional class ≥ 3, and the proportions of HFrEF and HFpEF were similar (61 [48%] vs. 65 [52%], respectively). Patients with HFrEF had a significantly higher history of anthracycline use, whereas fluoropyrimidine or other cytotoxic chemotherapy use was lower. Overall, 84% discontinued or interrupted anticancer therapy after HF onset. There were no significant differences in overall survival (log-rank p = 0.27) or cancer treatment continuation rates (log-rank p = 0.83) between HFpEF and HFrEF. All-cause mortality was associated with anemia (odds ratio [OR]: 3.46, 95% confidence interval [CI]; 1.36-8.82, p = 0.009) and performance status ≥ 3 (OR: 3.13, 95% CI; 1.18-8.26, p = 0.021), but not with LVEF. In patients who developed HF after anticancer treatment, HFrEF and HFpEF occurred at similar rates. There were no significant differences in overall survival or cancer treatment continuation between groups. Anemia and poor performance status, but not LVEF, independently predicted all-cause mortality.
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