Department of Medicine - Division of Hematology/Oncology, Center for Clinical and Translational Science, UMass Chan Medical School, Worcester, Massachusetts, USA.
Br J Haematol. 2024 Apr;204(4):1137-1138. doi: 10.1111/bjh.19336. Epub 2024 Feb 9.
As we commemorate 50 years since the introduction of classical 7 + 3 induction chemotherapy for acute myeloid leukaemia (AML), we also embark upon new territory with the advent of novel targeted therapeutics, including BH3 mimetics. To date, we do not have much large-scale longitudinal data regarding the toxicities of such novel therapies. Johnson et al. perform a comprehensive analysis of cardiac toxicities with hypomethylating agents and venetoclax and offer valuable insight into risk-benefit analysis when considering front-line therapy for AML. Commentary on: Johnson et al. Cardiac events in newly diagnosed acute myeloid leukaemia during treatment with venetoclax + hypomethylating agents. Br J Haematol 2024;204:1232-1237.
在纪念引入经典的 7+3 诱导化疗治疗急性髓系白血病(AML)50 周年之际,随着新型靶向治疗药物(包括 BH3 模拟物)的出现,我们也进入了一个新的领域。迄今为止,我们还没有关于这些新型治疗药物毒性的大量大规模纵向数据。Johnson 等人对低甲基化药物和 venetoclax 的心脏毒性进行了全面分析,并在考虑 AML 一线治疗时对风险效益分析提供了有价值的见解。述评:Johnson 等人在 venetoclax+低甲基化药物治疗新发急性髓系白血病期间的心脏事件。Br J Haematol 2024;204:1232-1237。