4.6 Article

Decitabine-Intensified Modified Busulfan/Cyclophosphamide Conditioning Regimen Improves Survival in Acute Myeloid Leukemia Patients Undergoing Related Donor Hematopoietic Stem Cell Transplantation: A Propensity Score Matched Analysis

Journal

FRONTIERS IN ONCOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.844937

Keywords

decitabine; busulfan; cyclophosphamide; acute myeloid leukemia; related donor hematopoietic stem cell transplantation

Categories

Funding

  1. National Natural Science Foundation of China [81770134, 82100233]
  2. Beijing Medical Award Foundation of China [YXJL-2019-0163-0114]
  3. Chen Xiao-ping Foundation for the Development of Science and Technology of Hubei Province, China [CXPJJH12000009-114]

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This study found that decitabine-intensified myeloablative conditioning could reduce the incidence of acute graft-versus-host disease and improve the overall survival and GVHD-free relapse-free survival in patients with acute myeloid leukemia after related donor hematopoietic stem cell transplantation.
To identify the benefit of decitabine (Dec)-intensified myeloablative conditioning on the outcomes of patients with acute myeloid leukemia (AML) after related donor hematopoietic stem cell transplantation (HSCT), we performed a retrospective matched-pair study from a pool of 156 patients to evaluate Dec [20 mg/m(2)/day intravenously (i.v.) on days -11 to -7]-intensified modified busulfan/cyclophosphamide (mBuCy) conditioning regimen vs. mBuCy regimen in 92 AML patients, with 46 patients in each cohort. The cumulative incidence of grade II-IV acute graft-versus-host disease (aGVHD) was lower in the Dec group (15.2% +/- 0.3% vs. 32.6% +/- 0.5%, P = 0.033). Compared with mBuCy group (15.5% +/- 0.3%), a significantly higher proportion of limited chronic GVHD (cGVHD) in Dec group (35% +/- 0.6%) was observed (P = 0.025). Dec-intensified mBuCy conditioning was associated with better 2-year overall survival (OS) and GVHD-free relapse-free survival (GRFS) (81% +/- 6.2% vs. 59.4% +/- 7.5%, P = 0.03; 58.7% +/- 8.1% vs. 40.9% +/- 7.3%, P = 0.042; respectively). Our results also elucidated that the Dec group had better 2-year OS and lower 2-year cumulative incidence of relapse (CIR) in patients acquiring haploidentical HSCT than that of the mBuCy group (84.8% +/- 7.1% vs. 58.2% +/- 10.3%, P = 0.047; 17.9% +/- 0.8% vs. 40.0% +/- 1.0%, P = 0.036; respectively), which did not increase the treatment-related mortality and regimen-associated toxicities. Dec-intensified myeloablative regimen and high-risk stratification were the variables associated with OS, leukemia-free survival (LFS), and GRFS in multivariate analysis. In high-risk patients, no differences were found in CIR, OS, LFS, and GRFS between the two groups. These data indicated that Dec-intensified mBuCy conditioning regimen was associated with better survival than mBuCy regimen in AML patients, especially in patients undergoing haploidentical HSCT.

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