Abstract

BackgroundPost-transplant relapse remains a principal leading cause of failure after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with adult acute lymphoblastic leukemia (ALL). The aim of this study was to investigate the efficacy and safety of low-dose decitabine on the prevention of adult ALL relapse after allo-HSCT.MethodsIn this prospective study, we enrolled 34 patients with ALL who underwent allo-HSCT from August 2016 to April 2020 and received low-dose decitabine maintenance treatment after transplantation. The primary objectives were cumulative incidence of relapse rate (CIR), overall survival (OS), and disease-free survival (DFS). The secondary objectives were graft-versus-host disease (GVHD) and safety.ResultsAmong the enrolled 34 patients, 6 patients relapsed and 6 patients died. The 2-year CIR, OS, and DFS were 20.2, 77.5, and 73.6%, respectively. Subgroup analysis revealed the 2-year CIR, OS, and DFS rates of 12 patients with T-ALL/lymphoblastic lymphoma (LBL) were 8.3, 90, and 81.5%, respectively. None of the seven patients with T-ALL relapsed. During maintenance treatment, only one patient (2.9%) developed grade IV acute GVHD and four (11.8%) patients had severe chronic GVHD. Thirty-two patients (94.1%) developed only grade I to II myelosuppression, and two patients (5.8%) developed grade III to IV granulocytopenia.ConclusionsMaintenance treatment with low-dose decitabine after allo-HSCT may be used as a therapeutic option to reduce relapse in patients with adult ALL, especially in patients with T-ALL. Our findings require confirmation in larger-scale controlled trials.Clinical Trial RegistrationChinese Clinical Trials Registry, identifier ChiCTR1800014888.

Highlights

  • Post-transplant relapse remains a leading cause of failure after allogeneic hematopoietic stem cell transplantation

  • Only one patient (2.9%) developed grade IV acute graft-versus-host disease (GVHD) and four (11.8%) patients had severe chronic GVHD

  • Maintenance treatment with low-dose decitabine after allo-HSCT may be used as a therapeutic option to reduce relapse in patients with adult acute lymphoblastic leukemia (ALL), especially in patients with T-ALL

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Summary

Introduction

Post-transplant relapse remains a leading cause of failure after allogeneic hematopoietic stem cell transplantation (allo-HSCT). The downregulation of human leukocyte antigen II (HLA-II) molecules leads to the inability of donor T cells to recognize leukemic cells, which limits the use of DLI in the treatment of relapse after transplantation in patients with acute myeloid leukemia (AML) [4, 5], and the 3-year overall survival (OS) rate of these patients is only 10–20% [6]. It is urgent to explore novel approaches to prevent leukemia relapse after allo-HSCT in adult ALL. Post-transplant relapse remains a principal leading cause of failure after allogeneic hematopoietic stem cell transplantation (allo-HSCT) in patients with adult acute lymphoblastic leukemia (ALL). The aim of this study was to investigate the efficacy and safety of low-dose decitabine on the prevention of adult ALL relapse after allo-HSCT

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