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Comparison of Intensive Chemotherapy and Hypomethylating Agents before Allogeneic Stem Cell Transplantation for Advanced Myelodysplastic Syndromes: A Study of the Myelodysplastic Syndrome Subcommittee of the Chronic Malignancies Working Party of the European Society for Blood and Marrow Transplant Research.
Potter, Victoria T; Iacobelli, Simona; van Biezen, Anja; Maertens, Johann; Bourhis, Jean-Henri; Passweg, Jakob R; Yakhoub-Agha, Ibrahim; Tabrizi, Reza; Bay, Jacques-Olivier; Chevallier, Patrice; Chalandon, Yves; Huynh, Anne; Cahn, Jean Yves; Ljungman, Per; Craddock, Charles; Lenhoff, Stig; Russell, N H; Fegueux, Nathalie; Socié, Gerard; Bruno, Benedetto; Meijer, Ellen; Mufti, G J; de Witte, Theo; Robin, Marie; Kröger, Nicolaus.
Affiliation
  • Potter VT; Department of Haematological Medicine, Kings College Hospital, London, United Kingdom. Electronic address: victoriapotter@nhs.net.
  • Iacobelli S; Centro Interdipartimentale di Biostatistica e Bioinformatica, Università Tor Vergata, Roma, Italy.
  • van Biezen A; European Society for Blood and Marrow Transplant Research Data Office, Leiden University Medical Centre, Leiden, Netherlands.
  • Maertens J; Division of Hematology, Uz Gasthuisberg, Leuven, Belgium.
  • Bourhis JH; Division of Hematology, Institut Gustave Roussy, Villejuif, France.
  • Passweg JR; Division of Hematology, University Hospital of Basel, Basel, Switzerland.
  • Yakhoub-Agha I; Hôpital HURIEZ, Lille, France.
  • Tabrizi R; Division of Hematology, CHU, Bordeaux, France.
  • Bay JO; Service de Thérapie Cellulaire et d'hématologie clinique adulte, Hotel-Dieu, Clermont-Ferrand, France.
  • Chevallier P; Division of Hematology, CHU, Nantes, France.
  • Chalandon Y; Division of Hematology, HUG, Geneva, Switzerland.
  • Huynh A; Hopital de Purpan, Toulouse, France.
  • Cahn JY; Hématologie Clinique, Hospital A. Michallon, Grenoble, France.
  • Ljungman P; Department of Hematology, Karolinska University Hospital, Stockholm, Sweden.
  • Craddock C; Centre for Clinical Haematology, Queen Elizabeth Hospital, Birmingham, United Kingdom.
  • Lenhoff S; Department of Hematology, Skanes University Hospital, Lund, Sweden.
  • Russell NH; Nottingham City Hospital, Nottingham, United Kingdom.
  • Fegueux N; Départment d'Hématologie Clinique, Montpellier, France.
  • Socié G; Department of Hematologie-BMT, Hospital St. Louis, Paris, France.
  • Bruno B; S.S.C.V.D. Trapianto di Cellule Staminali, A.O.U. Citta della Salute e della Scienza di Torino Presidio Molinette, Torino, Italy.
  • Meijer E; Department of Hematology, VU University Medical Center, Amsterdam, Netherlands.
  • Mufti GJ; Department of Haematological Medicine, Kings College London, United Kingdom.
  • de Witte T; Department of Tumorimmunology Radboud University Medical Centre, Nijmegen, Netherlands.
  • Robin M; Division of Hematology - Bone Marrow Transplantation, Saint-Louis Hospital, Paris, France.
  • Kröger N; Department of Stem Cell Transplantation University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Biol Blood Marrow Transplant ; 22(9): 1615-1620, 2016 09.
Article in En | MEDLINE | ID: mdl-27264633
ABSTRACT
The European Society for Blood and Marrow Transplant Research data set was used to retrospectively analyze the outcomes of hypomethylating therapy (HMA) compared with those of conventional chemotherapy (CC) before hematopoietic stem cell transplantation (HSCT) in 209 patients with advanced myelodysplastic syndromes. Median follow-up was 22.1 months and the median age of the group was 57.6 years with 37% of the population older than > 60 years. The majority of patients (59%) received reduced-intensity conditioning and 34% and 27% had intermediate-2 and high international prognostic scoring system (IPSS) scores. At time of HSCT, 32% of patients did not achieve complete remission (CR) and 13% had primary refractory disease. On univariate analysis, outcomes at 3 years were not significantly different between HMA and CC for overall survival (OS), relapse-free survival (RFS), cumulative incidence of relapse (CIR), and nonrelapse mortality (NRM) OS (42% versus 35%), RFS (29% versus 31%), CIR (45% versus 40%), and NRM (26% versus 28%). Comparing characteristics of the groups, there were more patients < 55 years old, more patients in CR (68% versus 32%), and fewer patients with primary refractory disease in the CC group than in the HMA group (10% versus 19%, P < .001). Patients with primary refractory disease had worse outcomes than those in CR with regard to OS (hazard ratio [HR], 2.42; 95% confidence interval [CI], 1.41 to 4.13; P = .001), RFS (HR, 2.27; 95% CI, 1.37 to 3.76; P = .001), and NRM (HR, 2.49; 95% CI, 1.18 to 5.26; P = .016). In addition, an adverse effect of IPSS-R cytogenetic risk group was evident for RFS. In summary, outcomes after HSCT are similar for patients receiving HMA compared with those receiving CC, despite the higher proportion of patients with primary refractory disease in the HMA group.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myelodysplastic Syndromes / Antimetabolites, Antineoplastic / Antineoplastic Agents Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Biol Blood Marrow Transplant Journal subject: HEMATOLOGIA / TRANSPLANTE Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myelodysplastic Syndromes / Antimetabolites, Antineoplastic / Antineoplastic Agents Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Biol Blood Marrow Transplant Journal subject: HEMATOLOGIA / TRANSPLANTE Year: 2016 Document type: Article