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Salvage therapy using FLT3 inhibitors may improve long‐term outcome of relapsed or refractory AML in patients with FLT3‐ITD
Authors:Koichi Takahashi  Hagop Kantarjian  Naveen Pemmaraju  Michael Andreeff  Gautam Borthakur  Stefan Faderl  Guillermo Garcia‐Manero  Sherry Pierce  Rajyalakshmi Luthra  Marylou Cardenas‐Turanzas  Zeev Estrov  Farhad Ravandi  Jorge Cortes
Institution:1. Divison of Cancer Medicine, MD Anderson Cancer Center, The University of Texas, , Houston, TX, USA;2. Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, , Kyoto, Japan;3. Department of Leukemia, MD Anderson Cancer Center, The University of Texas, , Houston, TX, USA;4. Department of Hematopathology, MD Anderson Cancer Center, The University of Texas, , Houston, TX, USA
Abstract:To determine the long‐term efficacy of FLT3 inhibitors (FLT3i) in the salvage setting for relapsed and refractory (rel/ref) acute myeloid leukemia (AML) with FLT3 internal tandem duplication (AML FLT3‐ITD), we conducted a retrospective study of 120 patients with rel/ref AML FLT3‐ITD who received salvage therapy with either FLT3i‐containing regimen (FLT3i group, N = 45) or conventional cytotoxic regimen (conventional group, N = 75). The median overall survival (OS) after the first salvage in the FLT3i group was 6·9 vs. 4·6 months in the conventional group (P = 0·17). The OS was better in the FLT3i group among patients with initial complete remission (CR) duration ≤12 months or with primary refractory disease (6·9 vs. 3·7 months; P < 0·01). The OS was better when FLT3i was combined with cytotoxic agents versus monotherapy (17 vs. 4·8 months; P = 0·017). Multivariate analysis revealed that the use of FLT3i was an independent predictor of OS (hazard ratio 0·58; 95% confidence interval, 0·38–0·88). Incorporating FLT3i into salvage strategies may improve long‐term outcome of patients with AML FLT3‐ITD. Prospective studies to validate this conclusion are warranted.
Keywords:acute myeloid leukemia  FLT3 inhibitors  FLT3‐ITD
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