[Clinical Analysis for Patients with AML Treated after Allo-HSCT]

Qing-Yun Wang1, Yu-Jun Dong1, Ze-Yin Liang1

  • 1Department of Hematology, Peking University First Hospital, Beijing 100034, China.

Insights

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) improves survival for acute myeloid leukemia (AML) patients, but relapse remains a challenge. Maintenance therapy with hypomethylation agents and donor lymphocyte infusion (DLI) shows promise for relapsed AML post-transplant.

Area of Science:

  • Hematology
  • Oncology
  • Transplantation Medicine

Background:

  • Acute myeloid leukemia (AML) survival has improved with allogeneic hematopoietic stem cell transplantation (allo-HSCT).
  • Relapse remains a significant factor impacting long-term survival in AML patients post-allo-HSCT.
  • Identifying risk factors and effective salvage therapies for relapsed AML is crucial.

Purpose of the Study:

  • To identify risk factors influencing survival and relapse in AML patients undergoing allo-HSCT.
  • To investigate therapeutic strategies for managing AML relapse after allo-HSCT.

Main Methods:

  • Retrospective analysis of clinical data from 180 AML patients who achieved complete remission before allo-HSCT.
  • COX regression analysis was employed to determine risk factors for survival and relapse.

Main Results:

  • The 5-year overall survival (OS), event-free survival (EFS), and cumulative relapse rates were 74.3%, 42.5%, and 25.0%, respectively.
  • Independent risk factors for OS included high-risk status, adverse cytogenetics, CR2 at HSCT, and absence of cGvHD.
  • High-risk status, MRD positivity, adverse cytogenetics, and absence of cGVHD were associated with relapse; hypomethylation agents plus DLI improved OS in relapsed patients (2-year OS 62.5%).

Conclusions:

  • Allo-HSCT significantly enhances AML survival, yet relapse remains a primary determinant of patient outcomes.
  • Maintenance therapy combining hypomethylation agents with donor lymphocyte infusion (DLI) presents a potential effective treatment for relapsed AML post-allo-HSCT.
Abstract