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ACEIs and Beta Blockers Show Cardioprotective Effects in ChemotherapyACE Inhibitors and Beta Blockers May Protect Hearts During Chemotherapy

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Key Takeaway
ACEIs and beta blockers modestly preserve cardiac function and reduce heart failure risk during chemotherapy, but evidence quality is low.

An umbrella review of 35 meta-analyses (108 associations) evaluated the cardioprotective effects of ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), and beta blockers in patients undergoing chemotherapy. The primary outcome was preservation of left ventricular (LV) ejection fraction. ACEIs showed a mean difference of 4.22% (95% CI 1.56% to 6.88%) in LV ejection fraction preservation, while beta blockers showed a mean difference of 2.77% (95% CI 1.40% to 4.14%). Beta blockers also reduced the incidence of heart failure (RR 0.29, 95% CI 0.26 to 0.34) and cardiotoxicity (RR 0.44, 95% CI 0.26 to 0.75). Additionally, ACEIs reduced arrhythmias (RR 0.17, 95% CI 0.03 to 0.91). Beta blockers mitigated the decline in the E-wave to A-wave velocity ratio (MD 0.07, 95% CI 0.01 to 0.13). However, the certainty of evidence was low to very low for most outcomes, and no significant impact on hypotension was noted. The authors caution that routine prophylactic use is not yet recommended due to the lack of robust randomized controlled trials with standardized endpoints. Further high-quality research is needed to confirm these findings and establish definitive guidelines.

How this fits prior evidence

This umbrella review extends previous findings that beta-blockers may reduce cardiotoxicity risk during cancer therapy. It provides more specific data on ejection fraction preservation (MD 2.77% for beta blockers) and arrhythmia reduction (RR 0.17 for ACEIs), while also addressing the broader scope of ACE inhibitors and angiotensin receptor blockers in chemotherapy settings.

Researchers analyzed 35 meta-analyses to see how certain medications affect heart health in patients undergoing chemotherapy. The study looked at the effects of ACE inhibitors, angiotensin receptor blockers, and beta blockers on cardiac structure and function.

The findings suggest that both ACE inhibitors and beta blockers may help preserve left ventricular ejection fraction. Specifically, ACE inhibitors showed a mean difference of 4.22% and beta blockers showed an increase of 2.77%. Additionally, beta blockers were associated with a lower risk of heart failure and cardiotoxicity, while ACE inhibitors were linked to fewer arrhythmias.

While these results are promising, the researchers noted that the evidence for some findings is of low certainty. Because the study relied on various types of data rather than many high-quality trials, it is not yet recommended as a routine way to prevent heart issues. Patients should talk to their doctors about how these medications might fit into their specific treatment plan.

What this means for you:
Certain heart medications may offer some protection during chemotherapy, but evidence is currently limited.

Common questions

Can these medications help my heart during chemotherapy?

The study suggests that ACE inhibitors and beta blockers may offer some protection for heart function, such as preserving ejection fraction. However, because the evidence quality is currently low to moderate, doctors do not yet recommend using them routinely as a preventative measure for everyone.

What specific benefits did beta blockers show?

Beta blockers were associated with a 0.29 relative risk for heart failure and a 0.44 relative risk for cardiotoxicity. They also showed an increase in left ventricular ejection fraction by 2.77% and helped reduce the decline of E-wave to A-wave velocity.

Are there any risks or side effects mentioned?

The study did not report significant impacts on blood pressure (hypotension) for these medications. However, because many parts of the study had low certainty, you should consult your medical team to discuss how these findings apply to your specific health needs.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
BACKGROUND: Chemotherapy-induced cardiotoxicity is a major contributor to long-term cardiovascular morbidity among cancer survivors. ACE inhibitors (ACEIs), angiotensin receptor blockers and beta blockers have been proposed as prophylactic therapies; however, the robustness of existing evidence is unclear. We aimed to evaluate the strength, consistency and certainty of evidence from meta-analyses of randomised controlled trials (RCTs) assessing antihypertensive agents for preventing chemotherapy-related cardiac dysfunction. METHODS: We conducted an umbrella review of meta-analyses of RCTs following Preferred Reporting Items for Overviews of Reviews guidelines. Systematic searches were performed in PubMed, Embase and Cochrane Database through May 2025. Data were extracted and reanalysed using random-effects models (DerSimonian-Laird if ≥10 studies; Hartung-Knapp-Sidik-Jonkman if <10). Certainty of evidence was graded using the Grading of Recommendations, Assessment, Development and Evaluation (GRADE) framework. Primary outcomes included measures of cardiac function and structure; secondary outcomes were clinical and adverse events. RESULTS: 35 meta-analyses comprising 108 associations were included. Preservation of left ventricular (LV) ejection fraction was observed with ACEIs (mean difference, MD, 4.22%, 95% CI 1.56% to 6.88%; GRADE: very low) and beta blockers (MD 2.77%, 95% CI 1.40% to 4.14%; low). Beta blockers reduced ratio of the early (E-wave) to late (A-wave) velocity decline (MD 0.07, 95% CI 0.01 to 0.13; moderate). No significant effect was noted on LV dimensions or biomarkers. Beta blockers reduced incidence of heart failure (relative risk, RR, 0.29, 95% CI 0.26 to 0.34) and cardiotoxicity (RR 0.44, 95% CI 0.26 to 0.75), while ACEIs reduced arrhythmias (RR 0.17, 95% CI 0.03 to 0.91); certainty was low. No significant impact was detected on all-cause mortality or hypotension. CONCLUSIONS: ACEIs and beta blockers appear to confer modest cardioprotective effects during chemotherapy, particularly regarding systolic function and heart failure incidence, although with predominantly low-certainty evidence. Larger, robust RCTs with standardised endpoints are required before routine prophylactic use is recommended. PROSPERO REGISTRATION NUMBER: CRD420251046471.
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