Davide, P., Luca, F., David, B., Pooja, B., M, P.G., & C, D.C. (2026). Cardioprotective Effects of Prophylactic Angiotensin-Converting Enzyme Inhibitors in Anthracycline-Induced Cardiotoxicity: A Systematic Review and Meta-analysis of Randomized Trials.. Journal of cardiovascular pharmacology.
Davide P, Luca F, David B, Pooja B, M PG, C DC. Cardioprotective Effects of Prophylactic Angiotensin-Converting Enzyme Inhibitors in Anthracycline-Induced Cardiotoxicity: A Systematic Review and Meta-analysis of Randomized Trials.. Journal of cardiovascular pharmacology. 2026; PMID: 41774060
Davide P, Luca F, David B, et al. Cardioprotective Effects of Prophylactic Angiotensin-Converting Enzyme Inhibitors in Anthracycline-Induced Cardiotoxicity: A Systematic Review and Meta-analysis of Randomized Trials.[J]. Journal of cardiovascular pharmacology. 2026.
@article{davide2026,
author = {Pizzi Davide and Fazzini Luca and Bassil David and Bajaj Pooja and Pugliesi Giordano M and Dessalvi Christian C},
title = {Cardioprotective Effects of Prophylactic Angiotensin-Converting Enzyme Inhibitors in Anthracycline-Induced Cardiotoxicity: A Systematic Review and Meta-analysis of Randomized Trials.},
journal = {Journal of cardiovascular pharmacology},
year = {2026},
note = {PMID: 41774060},
}
TY - JOUR AU - Pizzi Davide AU - Fazzini Luca AU - Bassil David AU - Bajaj Pooja AU - Pugliesi Giordano M AU - Dessalvi Christian C TI - Cardioprotective Effects of Prophylactic Angiotensin-Converting Enzyme Inhibitors in Anthracycline-Induced Cardiotoxicity: A Systematic Review and Meta-analysis of Randomized Trials. T2 - Journal of cardiovascular pharmacology PY - 2026 AN - PMID:41774060 ER -
This study aimed to evaluate the efficacy of angiotensin-converting enzyme inhibitors (ACEi) in preventing anthracycline-induced cardiotoxicity in patients undergoing anthracycline-based chemotherapy. PubMed, Embase, and Cochrane databases were searched for randomized controlled trials (RCTs) comparing ACEi with standard treatment/placebo for cardiotoxicity prevention in patients undergoing anthracycline-based chemotherapy. We pooled outcomes of echocardiographic and cardiac biomarker changes. A random-effects model was used for all outcomes. We included 7 RCTs with 686 patients, of whom 346 (50%) received prophylaxis with ACEi. The most common malignancy was breast cancer, and the follow-up ranged from 6 to 31 months. Prophylactic use of ACEi was associated with a significantly smaller reduction in left ventricular ejection fraction (LVEF) compared with the control group {mean difference (MD) -5% [95% confidence interval (CI) -8% to -2%]; P < 0.010}. Subgroup analysis limited to studies excluding trastuzumab from the chemotherapy regimens showed no significant difference [MD -7% (95% CI -16% to 2%); P = 0.110]. By contrast, in studies including trastuzumab-containing regimens, ACEi demonstrated a statistically significant effect in limiting LVEF reduction [MD -3%, (95% CI -4 to -1); P < 0.010]. Diastolic function (E/A ratio) changes [MD 0.0 (95% CI -0.1 to 0.09); I 2 = 36.3%] and relative risk of increased troponin I at follow-up [Risk-Ratios 0.58 (95% CI 0.17-1.94); I 2 = 69.6%] were not statistically significant. Prophylactic ACEi administration in patients undergoing anthracycline-based chemotherapy was associated with a smaller decline in LVEF. This protective role may be more relevant in patients also receiving trastuzumab. More powered and longer follow-up studies are needed to confirm these findings.