Senapati Jayastu, Kadia Tapan Mahendra
Department of Leukemia, MD Anderson Cancer Center, 1515 Holcombe Blvd. - Unit 428, Houston, 77030, USA.
Curr Treat Options Oncol. 2022 Mar;23(3):359-380. doi: 10.1007/s11864-022-00952-6. Epub 2022 Mar 8.
Treatment options in acute myeloid leukemia (AML) have improved significantly over the last decade with better understanding of disease biology and availability of a multitude of targeted therapies. The use of FLT3 inhibitors (FLT3i) in FLT3-mutated (FLT3) AML is one such development; however, the clinical decisions that govern their use and dictate the choice of the FLT3i are evolving. Midostaurin and gilteritinib are FDA-approved in specific situations; however, available data from clinical trials also shed light on the utility of sorafenib maintenance post-allogeneic stem cell transplantation (allo-SCT) and quizartinib as part of combination therapy in FLT3 AML. The knowledge of the patient's concurrent myeloid mutations, type of FLT3 mutation, prior FLT3i use, and eligibility for allo-SCT helps to refine the choice of FLT3i. Data from ongoing studies will further precisely define their use and help in making more informed choices. Despite improvements in FLT3i therapy, the definitive aim is to enable the eligible patient with FLT3 AML (esp. ITD) to proceed to allo-SCT with regimens containing FLT3i incorporated prior to SCT and as maintenance after SCT.
在过去十年中,随着对疾病生物学的深入了解以及多种靶向治疗方法的出现,急性髓系白血病(AML)的治疗选择有了显著改善。在FLT3突变(FLT3)的AML中使用FLT3抑制剂(FLT3i)就是这样一种进展;然而,指导其使用并决定FLT3i选择的临床决策正在不断演变。米哚妥林和吉瑞替尼在特定情况下已获得美国食品药品监督管理局(FDA)批准;不过,临床试验的现有数据也揭示了索拉非尼在异基因干细胞移植(allo-SCT)后维持治疗的效用,以及 quizartinib作为FLT3 AML联合治疗一部分的效用。了解患者同时存在的髓系突变、FLT3突变类型、既往FLT3i使用情况以及allo-SCT的资格,有助于优化FLT3i的选择。正在进行的研究数据将进一步精确界定它们的使用方式,并有助于做出更明智的选择。尽管FLT3i治疗有所改善,但最终目标是使符合条件的FLT3 AML患者(尤其是伴有内部串联重复突变[ITD]的患者)能够接受含有在SCT前加入并在SCT后作为维持治疗的FLT3i的方案进行allo-SCT。