Unrelated donor hematopoietic stem cell transplantation for the treatment of non-malignant genetic diseases: An alemtuzumab based regimen is associated with cure of clinical disease; earlier clearance of alemtuzumab may be associated with graft rejection

Am J Hematol. 2015 Nov;90(11):1021-6. doi: 10.1002/ajh.24141. Epub 2015 Oct 12.

Abstract

Hematopoietic stem cell transplantation (HSCT) with matched unrelated donors (MUD), offers potentially curative therapy for patients with non-malignant genetic diseases. In this pilot study conducted from 2006 to 2014, we report the outcomes of 15 patients with non-malignant genetic diseases who received a myeloablative regimen with a reduced cyclophosphamide dose, adjunctive serotherapy and MUD HSCT [intravenous alemtuzumab (52 mg/m(2) ), busulfan (16 mg/kg), fludarabine (140mg/m(2) ), and cyclophosphamide (105 mg/kg)]. Graft-versus-host-disease (GVHD) prophylaxis consisted of tacrolimus/cyclosporine and methylprednisolone. Median (range) time to neutrophil engraftment (>500 cells/µL) and platelet engraftment (>20,000/mm(3) ) were 15 (12-28) and 25 (17-30) days, respectively. At a median follow-up of 2 (0.2-5.4) years, the overall survival (OS) was 93.3% (95% CI: 0.61-0.99) and disease-free survival (DFS) was 73.3% (95% CI: 0.44-0.89). Among this small sample, earlier alemtuzumab clearance was significantly associated with graft rejection (P = 0.047), earlier PHA response (P = 0.009) and a trend toward earlier recovery of recent thymic emigrants (RTE) (P = 0.06). This regimen was associated with durable donor engraftment and relatively low rates of regimen related toxicity (RRT); future alemtuzumab pharmacokinetic studies may improve outcomes, by allowing targeted alemtuzumab clearance to reduce graft rejection and promote more rapid immune reconstitution.

MeSH terms

  • Adolescent
  • Alemtuzumab
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Busulfan / therapeutic use
  • Child
  • Child, Preschool
  • Cyclophosphamide / therapeutic use
  • Cyclosporine / therapeutic use
  • Drug Administration Schedule
  • Female
  • Gene Expression
  • Genetic Diseases, Inborn / drug therapy*
  • Genetic Diseases, Inborn / genetics
  • Genetic Diseases, Inborn / mortality
  • Genetic Diseases, Inborn / pathology
  • Graft Rejection / genetics
  • Graft Rejection / mortality
  • Graft Rejection / pathology
  • Graft Rejection / prevention & control*
  • Graft vs Host Disease / genetics
  • Graft vs Host Disease / mortality
  • Graft vs Host Disease / pathology
  • Graft vs Host Disease / prevention & control*
  • HLA Antigens / genetics
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Infant
  • Male
  • Methylprednisolone / therapeutic use
  • Myeloablative Agonists / therapeutic use*
  • Pilot Projects
  • Survival Analysis
  • Tacrolimus / therapeutic use
  • Transplantation Conditioning
  • Transplantation, Homologous
  • Unrelated Donors
  • Vidarabine / analogs & derivatives
  • Vidarabine / therapeutic use

Substances

  • Antibodies, Monoclonal, Humanized
  • HLA Antigens
  • Immunosuppressive Agents
  • Myeloablative Agonists
  • Alemtuzumab
  • Cyclosporine
  • Cyclophosphamide
  • Vidarabine
  • Busulfan
  • fludarabine
  • Tacrolimus
  • Methylprednisolone