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Characteristics and Outcomes of Adult Patients in the PETHEMA Registry with Relapsed or Refractory FLT3 -ITD Mutation-Positive Acute Myeloid Leukemia.

David Martínez-CuadrónJosefina SerranoJosé Mário MarizCristina GilMar TormoPilar Martínez-SánchezEduardo Rodríguez-ArbolíRaimundo García-BoyeroCarlos Rodríguez-MedinaCarmen Martínez-ChamorroMarta PoloJuan BerguaEliana AguiarMaría L AmigoPilar HerreraJuan Manuel Alonso-DomínguezTeresa Bernal Del CastilloAna EspadanaMaría J SayasLorenzo AlgarraMaria Vidriales VicenteGraça VasconcelosSusana VivesManuel Mateo Pérez EncinasAurelio LópezVíctor NoriegaMaría García-FortesMaría C ChillónJuan I Rodríguez-GutiérrezMaría-José CalasanzJorge Labrador-GomezJuan A LópezBlanca BoludaRebeca Rodríguez-VeigaJoaquin Martinez LopezEva BarragánMiguel Angel SanzPau Montesinosnull On Behalf Of The Pethema Group
Published in: Cancers (2022)
This retrospective study investigated outcomes of 404 patients with relapsed/refractory (R/R) FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) acute myeloid leukemia (AML) enrolled in the PETHEMA registry, pre-approval of tyrosine kinase inhibitors. Most patients (63%) had received first-line intensive therapy with 3 + 7. Subsequently, patients received salvage with intensive therapy ( n = 261), non-intensive therapy ( n = 63) or supportive care only ( n = 80). Active salvage therapy (i.e., intensive or non-intensive therapy) resulted in a complete remission (CR) or CR without hematological recovery (CRi) rate of 42%. More patients achieved a CR/CRi with intensive (48%) compared with non-intensive (19%) salvage therapy ( p < 0.001). In the overall population, median overall survival (OS) was 5.5 months; 1- and 5-year OS rates were 25% and 7%. OS was significantly ( p < 0.001) prolonged with intensive or non-intensive salvage therapy compared with supportive therapy, and in those achieving CR/CRi versus no responders. Of 280 evaluable patients, 61 (22%) had an allogeneic stem-cell transplant after they had achieved CR/CRi. In conclusion, in this large cohort study, salvage treatment approaches for patients with FLT3 -ITD mutated R/R AML were heterogeneous. Median OS was poor with both non-intensive and intensive salvage therapy, with best long-term outcomes obtained in patients who achieved CR/CRi and subsequently underwent allogeneic stem-cell transplant.
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