Department of Hematology, Hemostasis, Oncology & Stem Cell Transplantation, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Servier International, 92284, Suresnes, France.
Future Oncol. 2023 Apr;19(11):789-810. doi: 10.2217/fon-2022-1286. Epub 2023 May 12.
To review clinical evidence for current and emerging treatments for patients with acute myeloid leukemia (AML) who are ineligible for first-line induction chemotherapy. A systematic literature review was performed (28 October 2021) to identify clinical outcomes including overall survival (OS), event-free survival (EFS), relapse-free survival (RFS) and adverse events (AEs). Of 233 references that met prespecified criteria, 26 studies were included. Adding targeted therapies (venetoclax/ivosidenib) to hypomethylating agents (HMAs) yielded better OS hazard ratios (HRs) (0.44-0.66) and EFS HRs (0.33-0.63) compared with other agents. AEs were more frequent with combination therapies than control arms, except with ivosidenib plus azacitidine. Targeted therapy combined with a HMA shows the most promising results in this difficult-to-treat population.
回顾不适合一线诱导化疗的急性髓系白血病(AML)患者的现有和新兴治疗方法的临床证据。进行了系统的文献回顾(2021 年 10 月 28 日),以确定包括总生存期(OS)、无事件生存期(EFS)、无复发生存期(RFS)和不良事件(AE)在内的临床结局。在符合预设标准的 233 篇参考文献中,纳入了 26 项研究。与其他药物相比,靶向治疗(venetoclax/ivosidenib)联合低甲基化剂(HMAs)可获得更好的 OS 风险比(HR)(0.44-0.66)和 EFS HR(0.33-0.63)。除ivosidenib 加阿扎胞苷外,联合治疗组的 AE 发生率高于对照组。在这种难以治疗的人群中,靶向治疗联合 HMA 显示出最有希望的结果。