Blood and marrow transplantation for sickle cell disease: Is less more?

Research output: Contribution to journalArticle

Abstract

Blood and marrow transplantation is a curative therapy for patients with sickle cell disease yet this option is seldom used. Clinical studies have shown however that children transplanted for this condition can achieve excellent results. In children with sickle cell disease transplanted following conditioning with busulfan, cyclophosphamide, and anti-thymocyte globulin, cure rates in excess of 80% can be obtained when an HLA-matched sibling is used as the donor. However, the large majority of patients with sickle cell disease will not have such a donor, or will not be able to tolerate high dose conditioning regimens. Therefore novel approaches such as non-myeloablative regimes, and alternative donors such as haploidentical, unrelated, or cord blood grafts are currently being explored in clinical trials. Recent reports on non-myeloablative conditioning (HLA-matched or haploidentical donors) highlight the safety and efficacy of these approaches with low mortality and high efficacy suggesting that in the near future non-myeloablation could be the preferred type of conditioning and donor availability will not be a barrier anymore to proceed to transplant. This review will focus on the results obtained when bone marrow transplants are used to treat sickle cell disease and will discuss the results obtained with these novel approaches.

Original languageEnglish (US)
Pages (from-to)243-248
Number of pages6
JournalBlood Reviews
Volume28
Issue number6
DOIs
StatePublished - Jan 1 2014

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Keywords

  • Alternative donors
  • Bone marrow transplant
  • Graft-versus-host disease
  • Sickle cell disease

ASJC Scopus subject areas

  • Hematology
  • Oncology

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