Seminars in Hematology
Volume 44, Issue 4 , Pages 259-266, October 2007

Acute Myeloid Leukemia and the Position of Autologous Stem Cell Transplantation

  • Dimitri A. Breems

      Affiliations

    • Department of Hematology, Hospital Network Antwerp, General Hospital Stuivenberg, Antwerp, Belgium.
  • ,
  • Bob Löwenberg

      Affiliations

    • Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
    • Corresponding Author InformationAddress correspondence to Bob Löwenberg, MD, PhD, Erasmus University Medical Center, Department of Hematology, PO Box 2040, 3000 CA Rotterdam, The Netherlands.

Most adult patients with acute myeloid leukemia (AML) who reach a complete remission (CR) after induction chemotherapy will relapse if they do not receive further therapy. Autologous stem cell transplantation (SCT) represents one of the options of postremission therapy in AML. Here we discuss the therapeutic impact of consolidation treatment with autologous SCT that has been studied extensively. Meta-analyses of published randomized trials using bone marrow as the source of stem cells show a modest improvement of disease-free survival as compared to nonmyeloablative chemotherapy. However, there is no apparent improvement of overall survival, probably due to the slightly increased mortality associated with autologous bone marrow transplantation (BMT). Subsequently, the value of autologous SCT in different prognostic subsets of AML is discussed. Autologous mobilized peripheral blood stem cell (PBSC) transplantation offers a much faster hematopoietic recovery and is associated with reduced morbidity and treatment-related mortality. To fully appreciate the role of autologous PBSC transplantation, the results of a recently closed randomized trial must be awaited.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0037-1963(07)00119-9

doi:10.1053/j.seminhematol.2007.08.002

Seminars in Hematology
Volume 44, Issue 4 , Pages 259-266, October 2007