Current status of reduced-intensity-conditioning allogeneic stem cell transplantation for acute myeloid leukemia

Haematologica. 2007 Apr;92(4):533-41. doi: 10.3324/haematol.10867.

Abstract

Allogeneic stem cell transplantation (allo-SCT) is the most efficient antileukemic treatment for acute myeloblastic leukemia (AML). However, elderly patients can rarely benefit from standard myeloablative allo-SCT because of an unacceptable rate of procedure-related toxicities. This point is critical when considering AML patients in first complete remission. The development of the so-called reduced-intensity conditioning (RIC) regimens appears to decrease allo-SCT-related toxicities, and has emerged as an attractive modality in AML patients not eligible for standard allo-SCT. Such RIC regimens aim primarily to provide the immune graft-versus-leukemia effect while causing little toxicity. Of note, treatment-related toxicity appears to be lower with RIC regimens as compared to standard myeloablative regimens. Nevertheless, toxicity might represent only one aspect of the problem, since AML encompasses a group of chemosensitive diseases, raising concerns that significant reduction of the intensity of the preparative regimen may have a negative impact on long-term leukemic control. Furthermore, no prospective studies have been reported thus far establishing RIC allo-SCT as the preferred option in AML. Investigators are currently faced with a dilemma on how to optimize the potential role of RIC allo-SCT in AML patients, while delivering minimal myeloablation and maximizing allogeneic immunotherapy. The aim of this review is to analyze the available research evidence in this field.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / adverse effects
  • Antilymphocyte Serum / administration & dosage
  • Antilymphocyte Serum / adverse effects
  • Antineoplastic Agents, Alkylating / administration & dosage
  • Antineoplastic Agents, Alkylating / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bone Marrow Diseases / chemically induced
  • Bone Marrow Diseases / prevention & control
  • Clinical Trials as Topic / statistics & numerical data
  • Combined Modality Therapy
  • Disease-Free Survival
  • Female
  • Graft vs Leukemia Effect
  • Hematopoietic Stem Cell Transplantation* / mortality
  • Hematopoietic Stem Cell Transplantation* / statistics & numerical data
  • Humans
  • Leukemia, Myeloid / drug therapy
  • Leukemia, Myeloid / surgery*
  • Lymphocyte Depletion
  • Male
  • Middle Aged
  • Recurrence
  • Remission Induction
  • Survival Analysis
  • T-Lymphocytes
  • Time Factors
  • Transplantation Conditioning / adverse effects
  • Transplantation Conditioning / methods*
  • Transplantation Conditioning / mortality
  • Transplantation Conditioning / statistics & numerical data
  • Transplantation, Homologous
  • Treatment Outcome
  • Vidarabine / administration & dosage
  • Vidarabine / adverse effects
  • Vidarabine / analogs & derivatives

Substances

  • Antibodies, Monoclonal
  • Antilymphocyte Serum
  • Antineoplastic Agents, Alkylating
  • Vidarabine
  • fludarabine