Allogeneic Stem Cell Transplantation for Myelodysplastic Syndrome Patients with a 5Q Deletion

  • Laurent Garderet
  • Dimitris Ziagkos
  • Anja van Biezen
  • Simona Iacobelli
  • Jürgen Finke
  • Johan Maertens
  • Liisa Volin
  • Per Ljungman
  • Patrice Chevallier
  • Jakob Passweg
  • Nicolaas Schaap
  • Dietrich Beelen
  • Arnon Nagler
  • Didier Blaise
  • Xavier Poiré
  • Ibrahim Yakoub-Agha
  • Stig Lenhoff
  • Charles Craddock
  • Rik Schots
  • Alessandro Rambaldi
  • Jaime Sanz
  • Pavel Jindra
  • Ghulam J Mufti
  • Marie Robin
  • Nicolaus Kröger

Abstract

The deletion (5q) karyotype (del [5q]) in patients with myelodysplastic syndrome (MDS) is the most common karyotypic abnormality in de novo MDS. An increased number of blasts and additional karyotypic abnormalities (del [5q]+) are associated with a poor outcome. We analyzed the outcome of allogeneic hematopoietic cell transplants (HCT) in patients suffering from MDS with only del (5q) or del (5q)+ . A total of 162 patients, of median age 54 years (range, 9 to 73), having MDS and del (5q) abnormalities received HCT from identical siblings (n = 87) or unrelated donors (n = 75). The cumulative incidence of nonrelapse mortality and relapse incidence at 4 years was 29% (95% CI, 22 to 36) and 46% (95% CI, 38 to 54), whereas the estimated 4 year survival, relapse-free and overall, was 25% (95% CI, 18 to 33) and 30% (95% CI, 23 to 38), respectively. In a multivariate analysis patients with del (5q) and a blast excess displayed poorer survival (hazard ratio, 2.38; 95% CI, 1.44 to 3.93; P < .001), whereas female recipient sex resulted in improved survival (hazard ratio, .61; 95% CI, .41 to .90; P = .01). We conclude that allogeneic HCT can cure a subset of patients with MDS and a del (5q) abnormality.

Bibliografische Daten

OriginalspracheEnglisch
ISSN1083-8791
DOIs
StatusVeröffentlicht - 03.2018
PubMed 29196078