Key result
Concomitant statins fail to preserve LVEF during chemotherapy but associate with better diastolic parameters.
Why the study?
Anthracycline-induced cardiotoxicity remains a major clinical challenge, and the association between statin use and pulmonary hemodynamic changes during anthracycline chemotherapy remains largely unexplored.
Does statin co-administration improve echocardiographic parameters in adult patients receiving anthracycline chemotherapy?
Cohort (n=285)
No
Does statin co-administration improve echocardiographic parameters in adult patients receiving anthracycline chemotherapy?
Mean Difference: 0.28 (95% CI -1.11–1.66)
Absolute Event Rate: -1.6% vs -4.3%
p-value: p=0.694
In patients receiving anthracycline chemotherapy, concomitant statin therapy was associated with preserved diastolic function and smaller changes in pulmonary artery pressure, but not with significant differences in left ventricular systolic function.
Statin co-administration was associated with preserved diastolic parameters without LVEF benefit; hypothesis-generating and requires prospective trials before practice change.
Background: Anthracycline-induced cardiotoxicity remains a major clinical challenge in oncology. The association between statin use and pulmonary hemodynamic changes during anthracycline chemotherapy remains largely unexplored. Methods: The primary endpoint was change in left ventricular ejection fraction from baseline to 12 months. Secondary endpoints included changes in left ventricular end-systolic volume index and mean e’ velocity. Exploratory endpoints included changes in other diastolic parameters, all estimated systolic pulmonary artery pressure (SPAP)-derived variables, and the descriptive incidence of cancer therapeutics-related cardiac dysfunction (CTRCD). Analyses included multivariable linear regression, 1:1 propensity score matching with baseline echocardiographic parameters included in the matching model, and multiple imputation for missing SPAP data. Results: After confounder adjustment, statin use was independently associated with a milder decline in mean e’ velocity (β = 0.75 cm/s, 95% CI 0.41 to 1.09, p < 0.001) and a smaller reduction in E/A ratio (β = 0.06, 95% CI 0.01 to 0.11, p = 0.02). No significant between-group difference was observed for adjusted ejection fraction change (β = 0.28%, 95% CI −1.11 to 1.66, p = 0.694). Statin use was associated with lower relative change amplitude of estimated SPAP (β = −4.55%, 95% CI −7.34 to −1.76, p = 0.001), with no significant effect on signed mean change. A descriptive component analysis showed a smaller signed mean change in estimated right atrial pressure in the statin group, with no significant difference in tricuspid regurgitant pressure gradient change. This comparison cannot mathematically decompose the absolute-change SPAP endpoint. The incidence of study-defined CTRCD was numerically lower in the statin group (1.25% vs. 4.8%, OR 0.25, 95% CI 0.05 to 1.28, p = 0.15), but this difference was not statistically significant and the study was underpowered for this clinical endpoint. Conclusions: In this retrospective cohort, concomitant statin therapy was associated with smaller changes in diastolic parameters and lower relative change amplitude of estimated SPAP between baseline and 12 month follow-up. No significant independent association with left ventricular systolic function was observed after multivariable adjustment. These hypothesis-generating findings require confirmation in appropriately powered prospective multicenter studies before any clinical implications can be considered.
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Wang et al. (2026) conducted a cohort in Malignancies receiving anthracycline chemotherapy (n=285). Statin therapy vs. Non-statin users was evaluated on Change in left ventricular ejection fraction from baseline to 12 months (β = 0.28%, 95% CI -1.11 to 1.66, p=0.694). Concomitant statin therapy was not independently associated with left ventricular ejection fraction change but was associated with smaller changes in diastolic parameters and lower relative change amplitude of estimated SPAP.
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