Results of a prospective multicentre myeloablative double-unit cord blood transplantation trial in adult patients with acute leukaemia and myelodysplasia. Academic Article uri icon

Overview

abstract

  • Double-unit cord blood (CB) grafts may improve engraftment and relapse risk in adults with haematological malignancies. We performed a prospective high-dose myeloablative double-unit CB transplantation (CBT) trial in adults with high-risk acute leukaemia or myelodysplasia (MDS) between 2007 and 2011. The primary aim was to establish the 1-year overall survival in a multi-centre setting. Fifty-six patients (31 acute myeloid leukaemia, 19 acute lymphoblastic leukaemia, 4 other acute leukaemias, 2 myelodysplastic syndrome [MDS]) were transplanted at 10 centres. The median infused total nucleated cell doses were 2·62 (larger unit) and 2·02 (smaller unit) x 10(7) /kg. The cumulative incidence of day 100 neutrophil engraftment was 89% (95% confidence interval [CI]: 80-96). Day 180 grade II-IV acute graft-versus-host disease (GVHD) incidence was 64% (95%CI: 51-76) and 36% (95%CI: 24-49) of patients had chronic GVHD by 3-years. At 3-years post-transplant, the transplant-related mortality (TRM) was 39% (95%CI: 26-52), and the 3-year relapse incidence was 11% (95%CI: 4-21). With a median 37-month (range 23-71) follow-up of survivors, the 3-year disease-free survival was 50% (95%CI: 37-63). Double-unit CBT is a viable alternative therapy for high-risk acute leukaemia/ MDS in patients lacking a matched unrelated donor. This is especially important for minority patients. The relapse incidence was low but strategies to ameliorate TRM are needed.

authors

  • Barker, Juliet
  • Fei, Mingwei
  • Karanes, Chatchada
  • Horwitz, Mitchell
  • Devine, Steven
  • Kindwall-Keller, Tamila L
  • Holter, Jennifer
  • Adams, Alexia
  • Logan, Brent
  • Navarro, Willis H
  • Riches, Marcie

publication date

  • October 1, 2014

Research

keywords

  • Fetal Blood
  • Leukemia
  • Myelodysplastic Syndromes

Identity

PubMed Central ID

  • PMC5557396

Scopus Document Identifier

  • 84921434405

Digital Object Identifier (DOI)

  • 10.1111/bjh.13136

PubMed ID

  • 25272241

Additional Document Info

volume

  • 168

issue

  • 3