New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years

Blood. 2004 Aug 15;104(4):1201-3. doi: 10.1182/blood-2003-08-2800. Epub 2004 Mar 23.

Abstract

When prepared for transplantation with busulfan (BU) 14 mg/kg and cyclophosphamide (CY) 120 to 160 mg/kg, patients with thalassemia in risk class 3, aged younger than 17 years, who receive transplants from HLA-identical donors, had a 30% incidence of transplant rejection with recurrence of thalassemia. This, relatively poor, outcome was ascribed to insufficient immune suppression or to inadequate eradication of the thalassemic marrow, or both. In an attempt to enhance both immune suppression and eradication of the thalassemic clones, hydroxyurea, azathioprine, and fludarabine were added to the BU and CY. This regimen, called protocol 26, was applied to 33 consecutive patients with class 3 thalassemia aged younger than 17 years and was well tolerated with 93% survival. The incidence of recurrent thalassemia after the transplantation decreased from 30% to 8%.

Publication types

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

MeSH terms

  • Adolescent
  • Age Factors
  • Antineoplastic Agents / administration & dosage
  • Bone Marrow Transplantation / methods*
  • Bone Marrow Transplantation / mortality
  • Chelating Agents / administration & dosage
  • Child
  • Child, Preschool
  • Clinical Protocols
  • Deferoxamine / administration & dosage
  • Erythrocyte Transfusion
  • Female
  • Growth Substances / administration & dosage
  • Hematopoiesis / drug effects
  • Humans
  • Immunosuppressive Agents / administration & dosage
  • Male
  • Prognosis
  • Recurrence
  • Risk Assessment
  • Survival Analysis
  • Thalassemia / mortality
  • Thalassemia / therapy*

Substances

  • Antineoplastic Agents
  • Chelating Agents
  • Growth Substances
  • Immunosuppressive Agents
  • Deferoxamine