Salvage allogeneic hematopoietic cell transplantation with fludarabine and low-dose total body irradiation after rejection of first allografts. Academic Article uri icon

Overview

abstract

  • We summarized results in 38 consecutive patients (median age=56 years) with hematologic malignancies (n=35), aplastic anemia (n=2), or renal cell carcinoma (n=1), who underwent salvage hematopoietic cell transplantation (HCT) for allograft rejection. In 14 patients, the original donors were used for salvage HCT, and, in 24 cases, different donors were used. Conditioning for salvage HCT consisted of fludarabine (Flu) and either 3 or 4 Gy total body irradiation (TBI). Sustained engraftment was achieved in 33 patients (87%). Grafts were rejected in 5 patients (13%), 4 of whom had myelofibrosis. With a median follow-up of 2 years (range: 0.3 to 7.8 years), the 2- and 4-year estimated survivals were 49% and 42%, respectively. The 2-year relapse rate and nonrelapse mortality (NRM) were 36% and 24%, respectively. The 2-year cumulative incidences of grades II-IV acute and moderate-severe chronic graft-versus-host disease (aGVHD, cGVHD) were 42% and 41%, respectively. In this cohort, TBI dose, grafts from original versus different donors, related versus unrelated donors, and HCT comorbidity scores did not have an impact on outcomes. We concluded that graft rejection after allogeneic HCT could be overcome by salvage transplantation using conditioning with Flu and low-dose TBI.

authors

  • Gyurkocza, Boglarka
  • Cao, Thai M
  • Storb, Rainer F
  • Lange, Thoralf
  • Leisenring, Wendy
  • Franke, Georg N
  • Sorror, Mohamed
  • Hoppe, Richard
  • Maloney, David G
  • Negrin, Robert S
  • Shizuru, Judith A
  • Sandmaier, Brenda M

publication date

  • August 3, 2009

Research

keywords

  • Graft Rejection
  • Hematopoietic Stem Cell Transplantation
  • Living Donors
  • Myeloablative Agonists
  • Salvage Therapy
  • Transplantation Conditioning
  • Vidarabine
  • Whole-Body Irradiation

Identity

PubMed Central ID

  • PMC2757150

Scopus Document Identifier

  • 69849114854

Digital Object Identifier (DOI)

  • 10.1016/j.bbmt.2009.06.011

PubMed ID

  • 19747640

Additional Document Info

volume

  • 15

issue

  • 10