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 RambaldiJaime Sanz, Pavel Jindra, Ghulam J. Mufti, Marie Robin, Nicolaus Kröger

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

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.
Original languageEnglish
Pages (from-to)507-513
Number of pages7
JournalBiology of Blood and Marrow Transplantation
Volume24
Issue number3
Early online date28 Nov 2017
DOIs
Publication statusPublished - Mar 2018

Keywords

  • MDS
  • del (5q)
  • Allogeneic stem cell transplantation

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