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Outcomes after allogeneic hematopoietic cell transplant in patients diagnosed with blast phase of myeloproliferative neoplasms: A retrospective study from the Chronic Malignancies Working Party of the European Society for Blood and Marrow Transplantation.
Ortí, Guillermo; Gras, Luuk; Zinger, Nienke; Finazzi, Maria Chiara; Sockel, Katja; Robin, Marie; Forcade, Edouard; Avenoso, Daniele; Kröger, Nicolaus; Finke, Jürgen; Radujkovic, Aleksandar; Hunault-Berger, Mathilde; Schroyens, Wilfried; Zuckerman, Tsila; Bourhis, Jean Henri; Chalandon, Yves; Bloor, Adrian; Schots, Rik; de Wreede, Liesbeth C; Drozd-Sokolowska, Joana; Raj, Kavita; Polverelli, Nicola; Czerw, Tomasz; Hernández-Boluda, Juan Carlos; McLornan, Donal; Yakoub-Agha, Ibrahim.
Afiliación
  • Ortí G; Department of Hematology, Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • Gras L; EBMT Statistical Unit, Leiden, The Netherlands.
  • Zinger N; EBMT Leiden Study Unit, Leiden, The Netherlands.
  • Finazzi MC; Department of Oncology and Hematology, University of Milan and Papa Giovanni XXIII, Bergamo, Italy.
  • Sockel K; Medical Clinic I, University Hospital Dresden, TU Dresden, Germany.
  • Robin M; Hopital Saint Louis, APHP, Université de Paris Cité, Paris, France.
  • Forcade E; Service d'Hématologie Clinique et Thérapie Cellulaire, Bordeaux, France.
  • Avenoso D; Kings College Hospital, London, UK.
  • Kröger N; University Hospital Eppendorf, Hamburg, Germany.
  • Finke J; University of Freiburg, Freiburg, Germany.
  • Radujkovic A; University of Heidelberg, Heidelberg, Germany.
  • Hunault-Berger M; CHRU, Angers, France.
  • Schroyens W; Antwerp University Hospital (UZA), Antwerp, Edegem, Belgium.
  • Zuckerman T; Rambam Medical Center, Haifa, Israel.
  • Bourhis JH; Gustave Roussy Cancer Campus, Villejuif, France.
  • Chalandon Y; Hôpitaux Universitaire Genève, Département d'Oncologie, Service d'Hématologie, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
  • Bloor A; Christie NHS Trust Hospital, Manchester, UK.
  • Schots R; Universitair Ziekenhuis Brussel, Brussels, Belgium.
  • de Wreede LC; Leiden University Medical Center, Leiden, The Netherlands.
  • Drozd-Sokolowska J; University Clinical Centre, Medical University of Warsaw, Warsaw, Poland.
  • Raj K; University College London Hospital, London, UK.
  • Polverelli N; USD Trapianti di Midollo, Adulti, Brescia, Italy.
  • Czerw T; Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, Poland.
  • Hernández-Boluda JC; Department of Hematology, Hospital Clínico Universitario, Valencia, Spain.
  • McLornan D; Department of Stem Cell Transplantation, University College London Hospital, London, UK.
  • Yakoub-Agha I; CHU de Lille, Univ. Lille, INSERM U1286, Lille, France.
Am J Hematol ; 98(4): 628-638, 2023 04.
Article en En | MEDLINE | ID: mdl-36606718
ABSTRACT
Allogeneic hematopoietic cell transplant (allo-HCT) provides the only potential route to long-term remission in patients diagnosed with blast phase transformation of myeloproliferative neoplasm (BP-MPN). We report on a large, retrospective European Society for Blood and Marrow Transplantation registry-based study of BP-MPN patients undergoing allo-HCT. BP-MPN patients undergoing first allo-HCT between 2005 and 2019 were included. A total of 663 patients were included. With a median follow-up of 62 months, the estimated 3-year overall survival (OS) was 36% (95% confidence interval [CI], 32-36). Factors associated with lower OS were Karnofsky Performance Score (KPS) <90 (hazard ratio [HR] 1.65, p < .001) and active disease at allo-HCT (HR 1.45, p < .001), whereas patients undergoing allo-HCT more recently associated with a higher OS (HR 0.96, p = .008). In a selected patient's population, the 3-year OS of patients undergoing allo-HCT in complete response (CR) and with a KPS ≥90 was 60%. KPS < 90 (HR 1.4, p = .001) and active disease (HR 1.44, p = .0004) were associated with a lower progression-free survival (PFS). Conversely, most recent allo-HCT associated with a higher PFS (HR 0.96, p = .008). Active disease at allo-HCT (HR 1.34, p = .03) was associated with a higher cumulative incidence of relapse (RI) and allo-HCT in earlier calendar years (HR 0.96, p = .02) associated with a lower RI. Last, KPS < 90 (HR 1.91, p < .001), active disease (HR 1.74, p = .003) and allo-HCT from mismatched related donors were associated with a higher non-relapse mortality (HR 2.66, p = .003). In this large series of BP-MPN patients, about one third were alive at 3 years after transplantation. Patients undergoing allo-HCT in the more recent era, with a KPS ≥90 and in CR at transplant had a better prognosis.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Hematol Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Hematol Año: 2023 Tipo del documento: Article