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

•Outcome was studied of del 5q myelodysplastic syndrome patients undergoing allogeneic transplantation.•Patients with <5% bone marrow blasts and female recipients have the best prognosis.•Additional cytogenetic abnormalities do not influence the outcome. The deletion (5q) karyotype (del [5q]) in...

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Published inBiology of blood and marrow transplantation Vol. 24; no. 3; pp. 507 - 513
Main Authors Garderet, Laurent, Ziagkos, Dimitris, van Biezen, Anja, Iacobelli, Simona, Finke, Jürgen, Maertens, Johan, Volin, Liisa, Ljungman, Per, Chevallier, Patrice, Passweg, Jakob, Schaap, Nicolaas, Beelen, Dietrich, Nagler, Arnon, Blaise, Didier, Poiré, Xavier, Yakoub-Agha, Ibrahim, Lenhoff, Stig, Craddock, Charles, Schots, Rik, Rambaldi, Alessandro, Sanz, Jaime, Jindra, Pavel, Mufti, Ghulam J., Robin, Marie, Kröger, Nicolaus
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2018
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Abstract •Outcome was studied of del 5q myelodysplastic syndrome patients undergoing allogeneic transplantation.•Patients with <5% bone marrow blasts and female recipients have the best prognosis.•Additional cytogenetic abnormalities do not influence the outcome. 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.
AbstractList 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 &lt; .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.
•Outcome was studied of del 5q myelodysplastic syndrome patients undergoing allogeneic transplantation.•Patients with <5% bone marrow blasts and female recipients have the best prognosis.•Additional cytogenetic abnormalities do not influence the outcome. 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.
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.
Author Schaap, Nicolaas
Schots, Rik
Sanz, Jaime
Robin, Marie
Poiré, Xavier
Garderet, Laurent
Ziagkos, Dimitris
Jindra, Pavel
Yakoub-Agha, Ibrahim
Nagler, Arnon
Maertens, Johan
Mufti, Ghulam J.
Craddock, Charles
Volin, Liisa
Kröger, Nicolaus
Ljungman, Per
Chevallier, Patrice
van Biezen, Anja
Passweg, Jakob
Blaise, Didier
Rambaldi, Alessandro
Finke, Jürgen
Iacobelli, Simona
Lenhoff, Stig
Beelen, Dietrich
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  organization: Department of Haematology, University of Freiburg, Freiburg, Germany
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  organization: Department of Haematology, HUCH Comprehensive Cancer Center, Helsinki, Finland
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  organization: Department of Haematology, Karolinska University Hospital, Stockholm, Sweden
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  surname: Chevallier
  fullname: Chevallier, Patrice
  organization: Department of Haematology, CHU Nantes, Nantes, France
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  organization: Department of Haematology, University Hospital, Basel, Switzerland
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  organization: Department of Haematology, Radboud University—Nijmegen Medical Centre, Nijmegen, The Netherlands
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  fullname: Beelen, Dietrich
  organization: Department of Haematology, University Hospital, Essen, Germany
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  organization: Department of Haematology, Chaim Sheba Medical Center, Tel-Hashomer, Israel
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  fullname: Blaise, Didier
  organization: Department of Haematology, Centre de Recherche en Cancérologie de Marseille, Marseille, France
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  fullname: Poiré, Xavier
  organization: Department of Haematology, Cliniques Universitaires St. Luc, Brussels, Belgium
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  surname: Yakoub-Agha
  fullname: Yakoub-Agha, Ibrahim
  organization: Department of Haematology, Hospital Huriez, Lille, France
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  surname: Lenhoff
  fullname: Lenhoff, Stig
  organization: Department of Haematology, Skanes University Hospital, Lund, Sweden
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  surname: Craddock
  fullname: Craddock, Charles
  organization: Department of Haematology, Centre for Clinical Haematology, Birmingham, UK
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  surname: Schots
  fullname: Schots, Rik
  organization: Department of Haematology, Universitair Ziekenhuis Brussel, Brussels, Belgium
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  givenname: Alessandro
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  fullname: Rambaldi, Alessandro
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  givenname: Jaime
  surname: Sanz
  fullname: Sanz, Jaime
  organization: Department of Haematology, University Hospital La Fe, University of Valencia, Valencia, Spain
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  givenname: Pavel
  surname: Jindra
  fullname: Jindra, Pavel
  organization: Department of Haematology, Charles University Hospital, Pilsen, Czech Republic
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  givenname: Ghulam J.
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  organization: Department of Haematology, Hospital St. Louis, Paris, France
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  givenname: Nicolaus
  surname: Kröger
  fullname: Kröger, Nicolaus
  organization: Department of Haematology, University Hospital Eppendorf, Hamburg, Germany
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Keywords Allogeneic stem cell transplantation
MDS
del (5q)
Language English
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Snippet •Outcome was studied of del 5q myelodysplastic syndrome patients undergoing allogeneic transplantation.•Patients with <5% bone marrow blasts and female...
The deletion (5q) karyotype (del [5q]) in patients with myelodysplastic syndrome (MDS) is the most common karyotypic abnormality in de novo MDS. An increased...
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SubjectTerms Allogeneic stem cell transplantation
del (5q)
MDS
Medicin och hälsovetenskap
Title Allogeneic Stem Cell Transplantation for Myelodysplastic Syndrome Patients with a 5q Deletion
URI https://dx.doi.org/10.1016/j.bbmt.2017.11.017
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