Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Nov 1;10(1):75.
doi: 10.1186/s40959-024-00275-5.

Cardiotoxicity of venetoclax in patients with acute myeloid leukemia: comparison with anthracyclines

Affiliations

Cardiotoxicity of venetoclax in patients with acute myeloid leukemia: comparison with anthracyclines

Takeshi Onoue et al. Cardiooncology. .

Abstract

Venetoclax is a promising drug for patients with acute myeloid leukemia (AML) ineligible for anthracycline-based treatments. In rats, venetoclax is reported to cause myocardial injury. Our objectives were to report the frequency of cardiovascular (CV) events in patients treated with venetoclax, and, subsequently, to compare CV outcomes in matched patients treated with venetoclax or anthracyclines. Patients diagnosed with AML and treated with venetoclax or anthracyclines from January 2017 to July 2021 were identified. Major adverse cardiac events (MACE, including new-onset heart failure (HF), acute myocardial infarction, new onset atrial fibrillation (AF)) were recorded. Propensity-score method was then used to compare patients treated with venetoclax or anthracyclines. Patients treated with venetoclax (n=103) were older, with more hyperlipidemia than patients treated with anthracyclines (n=217). However, only 63% of patients treated with venetoclax underwent echocardiographic screening (vs. 93% of patients treated with anthracyclines, P< 0.001). Eighteen patients with venetoclax (17%) and 27 patients with anthracyclines (12%) developed MACE, including 10 % of new HF in each group. The median time to MACE was 8 days (interquartile range 5-98 days). In the matched cohort (n=132 patients), the cumulative incidence of MACE at one year was not different (17.5 % venetoclax, 9.2% anthracyclines, p =0.27). Thus, MACE incidence is similar in matched patients receiving venetoclax or anthracyclines. Close CV monitoring during the early phase of treatment may be helpful in patients treated with venetoclax.

Keywords: Atrial fibrillation; Cardiotoxicity; Heart failure; Venetoclax.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Flowchart of the Study
Fig. 2
Fig. 2
Cumulative incidence of Major Adverse Cardiac Events in a matched cohort of patients with AML treated with venetoclax or anthracyclines. Central Illustration. Major Adverse Cardiac Events in Patients with AML treated with anthracyclines or venetoclax. (Left) Flowchart and outcomes of the study. (Right) Cumulative incidence curve of MACE in a matched cohort of patients treated with venetoclax or anthracyclines
Fig. 3
Fig. 3
Central Illustration

References

    1. DiNardo CD, Jonas BA, Pullarkat V, et al. Azacitidine and Venetoclax in Previously Untreated Acute Myeloid Leukemia. N Engl J Med. 2020;383:617–29. - PubMed
    1. Tian F, Chen L, Qian ZM, et al. Ranking age-specific modifiable risk factors for cardiovascular disease and mortality: evidence from a population-based longitudinal study. EClinicalMedicine. 2023;64:102230. - PMC - PubMed
    1. AlAsmari AF, Alghamdi A, Ali N, et al. Venetoclax Induces Cardiotoxicity through Modulation of Oxidative-Stress-Mediated Cardiac Inflammation and Apoptosis via NF-kappaB and BCL-2 Pathway. Int J Mol Sci. 2022;23(11):6260. - PMC - PubMed
    1. Johnson IM, Bezerra ED, Farrukh F, et al. Cardiac events in patients with acute myeloid leukemia treated with venetoclax combined with hypomethylating agents. Blood Adv. 2022;6:5227–31. - PMC - PubMed
    1. Johnson IM, Karrar O, Rana M, et al. Cardiac events in newly diagnosed acute myeloid leukaemia during treatment with venetoclax + hypomethylating agents. Br J Haematol. 2024;204:1232–7. - PubMed

Grants and funding

LinkOut - more resources