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Blood ; 121(16): 3095-102, 2013 Apr 18.
Artículo en Inglés | MEDLINE | ID: mdl-23412094

RESUMEN

The optimal treatments for relapsed acute promyelocytic leukemia (APL) remain equivocal. We conducted a phase 2 study to evaluate the efficacy and feasibility of a sequential treatment consisting of induction and consolidation with arsenic trioxide (ATO), peripheral blood stem cell (PBSC) harvest after high-dose cytarabine chemotherapy, and autologous hematopoietic cell transplantation (HCT). Between 2005 and 2009, 35 patients (26 with hematologic and 9 with molecular relapse) were enrolled. Induction therapy resulted in complete remission in 81% of those with hematologic relapse, and most patients became negative for PML-RARα after the first ATO consolidation course, but 4 remained positive. Administration of the second ATO consolidation course further decreased the transcript levels in 3 patients. In total, 25 patients proceeded to PBSC harvest, all of whom successfully achieved the target CD34+ cell doses, and 23 underwent autologous HCT with PML-RARα-negative PBSC graft. Posttransplant relapse occurred in 3 patients, and there was no transplant-related mortality. With a median follow-up of 4.9 years, the 5-year event-free and overall survival rates were 65% and 77%, respectively. These findings demonstrate the outstanding efficacy and feasibility of the sequential treatment featuring ATO and autologous HCT for relapsed APL. This study was registered at http://www.umin.ac.jp/ctr/ as #C000000302.


Asunto(s)
Antineoplásicos/uso terapéutico , Arsenicales/uso terapéutico , Trasplante de Células Madre Hematopoyéticas/métodos , Leucemia Promielocítica Aguda/tratamiento farmacológico , Leucemia Promielocítica Aguda/cirugía , Recurrencia Local de Neoplasia/tratamiento farmacológico , Recurrencia Local de Neoplasia/cirugía , Óxidos/uso terapéutico , Adulto , Trióxido de Arsénico , Citarabina/uso terapéutico , Femenino , Estudios de Seguimiento , Humanos , Leucemia Promielocítica Aguda/genética , Masculino , Persona de Mediana Edad , Recurrencia Local de Neoplasia/genética , Proteínas de Fusión Oncogénica/genética , Inducción de Remisión , Transcripción Genética , Trasplante Autólogo , Adulto Joven
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