Best Practice & Research Clinical Haematology
Volume 19, Issue 2 , Pages 329-332, June 2006

How good is allogeneic transplantation for high-risk patients with AML?

  • Hans A. Messner, MD (Professor of Medicine, Director BMT Program)

      Affiliations

    • Corresponding Author InformationTel.: +1 4169462266; fax: +1 4169466485.

University Health Network, Princess Margaret Hospital, University of Toronto, 610 University Avenue, Toronto, Ont., Canada M5G 2M9

Patients with acute myeloid leukemia (AML) may differ significantly in their response to therapy and long-term outcome. A number of risk factors have been identified that characterize patients at diagnosis as well as during their clinical course. At diagnosis these parameters include age, cytogenetic configuration, hemopoietic elements, and a previous history of myelodysplasia or cytoreductive therapy for a preexisting malignancy. They are complemented by the response to induction therapy and subsequent treatments as well as by the duration of response. More recently, gene expression profiling of leukemic cells has added a new dimension to simultaneously assess biological risk factors that may ultimately lead to individualization of therapy. This presentation will review data to address the question of whether or not allogeneic transplants are effective in the management of patients with AML presenting with adverse cytogenetics and older age, showing a poor response to induction therapy, and relapsing after achieving a remission.

Keywords: AML, allogeneic BMT, risk factors

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: S1521-6926(05)00109-X

doi:10.1016/j.beha.2005.11.007

Best Practice & Research Clinical Haematology
Volume 19, Issue 2 , Pages 329-332, June 2006