Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Yale University and Yale Cancer Center, New Haven, CT, USA.
Leuk Lymphoma. 2023 Jan;64(1):188-196. doi: 10.1080/10428194.2022.2136952. Epub 2022 Oct 26.
FLT3, IDH1 and IDH2 inhibitors as well as venetoclax in combination with hypomethylating agents or low-dose cytarabine have expanded treatment options for patients with acute myeloid leukemia (AML). However, little data exist on the efficacy of venetoclax-based therapies in AML patients previously treated with FLT3 or IDH1/2 inhibitors. In this multicenter, retrospective cohort study, we included 44 patients who received venetoclax-based therapy after FLT3, IDH1 or IDH2 inhibitors. The overall response rate (ORR; composite of complete remission [CR]/CR with incomplete count recovery, partial remission, and morphologic leukemia free state) was 56.8% (18.2% CR) and a median overall survival of 9.2 months. While 6 out of 7 patients with mutations who had previously been treated with ivosidenib responded to venetoclax-based therapy, ITD mutations were associated with a lower response rate. Our data suggest that venetoclax can be an effective salvage therapy in patients previously treated with IDH1/2 or FLT3 inhibitors.
FLT3、IDH1 和 IDH2 抑制剂以及维奈托克联合低剂量阿糖胞苷或去甲基化药物已为急性髓系白血病(AML)患者的治疗选择提供了扩展。然而,先前接受过 FLT3 或 IDH1/2 抑制剂治疗的 AML 患者中,基于维奈托克的治疗的疗效数据很少。在这项多中心回顾性队列研究中,我们纳入了 44 名在接受 FLT3、IDH1 或 IDH2 抑制剂治疗后接受维奈托克治疗的患者。总体缓解率(ORR;完全缓解[CR]/CR 不完全计数恢复、部分缓解和形态学白血病无状态的复合)为 56.8%(18.2% CR),中位总生存期为 9.2 个月。尽管先前接受ivosidenib 治疗的 7 名 突变患者中有 6 名对维奈托克治疗有反应,但 ITD 突变与较低的反应率相关。我们的数据表明,维奈托克可作为先前接受 IDH1/2 或 FLT3 抑制剂治疗的患者的有效挽救治疗方法。