FLT3 Inhibitors as Maintenance Therapy after Allogeneic Stem-Cell Transplantation

被引:6
作者
Blackmon, Amanda [1 ]
Aldoss, Ibrahim [1 ]
Ball, Brian J. [1 ,2 ]
机构
[1] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplantat, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Dept Hematol & HCT, Div Leukemia, 1500 E Duarte Rd, Duarte, CA 91010 USA
关键词
FLT3; inhibitor; posttransplantation; maintenance; stem -cell transplantation; midostaurin; sorafenib; ACUTE MYELOID-LEUKEMIA; INTERNAL TANDEM DUPLICATION; MINIMAL RESIDUAL DISEASE; TYROSINE KINASE INHIBITORS; ACUTE MYELOGENOUS LEUKEMIA; PHASE-I; PROGNOSTIC-SIGNIFICANCE; SORAFENIB MAINTENANCE; ALLELIC RATIO; AML;
D O I
10.2147/BLCTT.S281252
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations in the FLT3 gene are associated with poor prognosis in patients with AML, even after consolidation with allogeneic hematopoietic cell transplantation (alloHCT) in first remission. Treatment failure in FLT3-mutated AML is largely driven by excessive risk of relapse compared to other genetic subtypes, including in patients post-alloHCT. As a result, there is substantial interest in studying posttransplant maintenance therapy in FLT3-mutated AML as an approach to optimize disease control and improve long-term outcomes. Clinical trials utilizing posttransplant FLT3 inhibitors, such as sorafenib and midostaurin, have shown feasibility, safety, and encouraging posttransplant outcomes, and there are ongoing studies using newer-generation tyrosine-kinase inhibitors as posttransplant maintenance therapy. Here, we review the toxicities and efficacy of FLT3 inhibitors as posttransplant maintenance, recommendations on the use of FLT3 inhibitors by international consensus guidelines, and highlight key remaining questions.
引用
收藏
页码:137 / 147
页数:11
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