Outcomes after Unrelated Umbilical Cord Blood Transplantation for Children with Osteopetrosis.

نویسندگان

  • Robert Chiesa
  • Annalisa Ruggeri
  • Annalisa Paviglianiti
  • Marco Zecca
  • Marta Gónzalez-Vicent
  • Victoria Bordon
  • Jerry Stein
  • Sarah Lawson
  • Sophie Dupont
  • Edoardo Lanino
  • Manuel Abecasis
  • Amal Al-Seraihy
  • Chantal Kenzey
  • Marc Bierings
  • Franco Locatelli
  • Eliane Gluckman
  • Ansgar Schulz
  • Andrew Gennery
  • Kristin Page
  • Joanne Kurtzberg
  • Vanderson Rocha
چکیده

Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for most children with osteopetrosis (OP). Timing of HSCT is critical; therefore, umbilical cord blood transplantation (UCBT) is an attractive option. We analyzed outcomes after UCBT in 51 OP children. Median age at UCBT was 6 months. Seventy-seven percent of the cord blood grafts had 0 or 1 HLA disparity with the recipient. Conditioning regimen was myeloablative (mostly busulfan-based in 84% and treosulfan-based in 10%). Antithymocyte globulin was given to 90% of patients. Median number of total nucleated and CD34+ cells infused was 14 × 107/kg and 3.4 × 105/kg, respectively. Median follow-up for survivors was 74 months. Cumulative incidence (CI) of neutrophil recovery was 67% with a median time to recovery of 23 days; 33% of patients had graft failure, 81% of engrafted patients had full donor engraftment, and 19% had mixed donor chimerism. Day 100 CI of acute graft-versus-host disease (grades II to IV) was 31% and 6-year CI of chronic graft-versus-host disease was 21%. Mechanical ventilation was required in 28%, and veno-occlusive disease was diagnosed in 16% of cases. Six-year overall survival rate was 46%. Comparative studies with other alternative donors should be performed to evaluate whether UCBT remains a valid alternative for children with OP without an HLA-matched donor.

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عنوان ژورنال:
  • Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

دوره 22 11  شماره 

صفحات  -

تاریخ انتشار 2016