Best Practice & Research Clinical Haematology
Volume 20, Issue 2 , Pages 311-327, June 2007

Disease relapse after haematopoietic stem cell transplantation: Risk factors and treatment

  • F. Dazzi, MD, PhD (Professor of Stem Cell Biology)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +44 208 383 2134; Fax: +44 208 742 9335.

Department of Haematology, Imperial College at Hammersmith Hospital, Du Cane Road, London W12 0NN, UK

Disease relapse is the commonest cause of treatment failure after allogeneic haematopoietic stem-cell transplantation. Adoptive immunotherapy based on donor lymphocyte infusions (DLI) has a prominent role in the management of disease recurrence. Although the highest remission rates are achieved in chronic myeloid leukaemia (CML), encouraging results have also been reported in chronic lymphoproliferative disorders. However, the experience of DLI in CML is not necessarily applicable to the management of lymphoproliferative diseases because of the heterogeneity of the conditioning regimens used in chronic lymphoid malignancies. We will review the role of DLI for different disease types in the context of conventional and reduced-intensity conditioning regimens. The factors influencing response and graft-versus-host disease as well as the optimal cell dose will be discussed. Finally, we will describe the main avenues currently being explored to improve the selectivity and efficacy of DLI.

Key words: allogeneic haematopoietic stem-cell transplantation, relapse, adoptive immunotherapy, donor lymphocyte infusions

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(06)00071-5

doi:10.1016/j.beha.2006.10.002

Best Practice & Research Clinical Haematology
Volume 20, Issue 2 , Pages 311-327, June 2007