Biology of Blood and Marrow Transplantation
Volume 14, Issue 4 , Pages 458-468, April 2008

Transplantation in Remission Improves the Disease-Free Survival of Patients with Advanced Myelodysplastic Syndromes Treated with Myeloablative T Cell-Depleted Stem Cell Transplants from HLA-Identical Siblings

  • Hugo Castro-Malaspina

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
    • Corresponding Author InformationCorrespondence and reprint requests: Hugo Castro-Malaspina, MD, Bone Marrow Transplantation Service, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021. Phone: (212) 639-8197. Fax: (212) 717-3371.
  • ,
  • Ann A. Jabubowski

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Esperanza B. Papadopoulos

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Farid Boulad

      Affiliations

    • Bone Marrow Transplantation Service, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • James W. Young

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Nancy A. Kernan

      Affiliations

    • Bone Marrow Transplantation Service, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Miguel A. Perales

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Trudy N. Small

      Affiliations

    • Bone Marrow Transplantation Service, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Katharine Hsu

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Michelle Chiu

      Affiliations

    • Bone Marrow Transplantation Service, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Glenn Heller

      Affiliations

    • Department of Epidemiology and Statistics, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Nancy H. Collins

      Affiliations

    • Bone Marrow Transplantation Service, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Suresh C. Jhanwar

      Affiliations

    • Cytogenetics Laboratory, Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Marcel van den Brink

      Affiliations

    • The Allogeneic Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Stephen D. Nimer

      Affiliations

    • Hematology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY
  • ,
  • Richard J. O'Reilly

      Affiliations

    • Bone Marrow Transplantation Service, Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY

Abstract 

From 1985 to 2004, 49 patients with advanced myelodysplastic syndromes (MDS) (≥5% blasts) or acute myeloid leukemia (AML) transformed from MDS underwent T cell depleted bone marrow or peripheral blood hematopoietic stem cell transplantation (HSCT) from HLA-identical siblings following conditioning with a myeloablative regimen that included total body irradiation (44 patients) or busulfan (5 patients). Thirty-six patients received chemotherapy (3 low dose and 33 induction doses) before conditioning, and 13 patients did not receive any chemotherapy. Prior to transplantation, 22 of the 36 treated patients were in hematologic remission; 4 were in a second refractory cytopenia phase (26 responders); 8 had failed to achieve remission; and 2 of the responders had progression or relapse of their MDS (10 failures). No post-transplantation pharmacologic prophylaxis for graft-versus-host disease (GVHD) was given. The median age was 48 yrs (range 13-61). Forty-five of the 49 patients engrafted; 2 had primary graft failure; and 2 died before engraftment. Only 3 patients developed acute GVHD (aGVHD) (grades I and III) and 1 chronic GVHD (cGVHD). At 3 yrs post-transplantation, the overall survival (OS) was 54% in the responders; 31% in the untreated group; and 0% in the failure group (P=.0004). The disease free survival (DFS) was 50%, 15% and 0% in each group respectively (P=.0008). In multivariate analysis, disease status before cytoreduction remained highly correlated with DFS (P<.001). The cumulative incidence (CI) of relapse at 2-yrs post-transplantation for the responders was 23%; for the untreated group was 38%; and for the failures was 50%. The CI of non-relapse mortality at 2-yrs post-transplantation, for the responders was 23%; for the untreated group was 38%; and for the failures was 40%. All survivors achieved a Karnofsky Performance Status (KPS) of ≥90. These results indicate that patients with advanced MDS who achieve and remain in remission or a second refractory cytopenia phase with chemotherapy before conditioning can achieve successful long-term remissions following a myeloablative T cell depleted allogeneic HSCT.

Key Words: Myelodysplastic syndromes, Hematopoietic stem cell transplantation, T cell depletion

 

PII: S1083-8791(08)00069-4

doi:10.1016/j.bbmt.2008.02.006

Biology of Blood and Marrow Transplantation
Volume 14, Issue 4 , Pages 458-468, April 2008