Allogeneic stem cell transplantation after reduced-intensity conditioning in patients with myelofibrosis: a prospective, multicenter study of the Chronic Leukemia Working Party of the European Group for Blood and Marrow Transplantation

Nicolaus Kröger(Universität Hamburg), Ernst Holler(University Hospital Regensburg), Guido Kobbe(Düsseldorf University Hospital), Martin Bornhäuser, Rainer Schwerdtfeger(Deutsche Klinik für Diagnostik), H. Baurmann(Deutsche Klinik für Diagnostik), Arnon Nagler(Sheba Medical Center), Wolfgang Bethge(University Children's Hospital Tübingen), Matthias Stelljes(University Hospital Münster), Lutz Uharek, Hannes Wandt(Nuremberg Hospital), Andreas Burchert(Philipps University of Marburg), Paolo Corradini(University of Milan), Jörg Schubert, Martin Kaufmann(Robert Bosch Hospital), Peter Dreger(Heidelberg University), Gerald Wulf(Universitätsmedizin Göttingen), Hermann Einsele(Universitätsklinikum Würzburg), Tatjana Zabelina(Universität Hamburg), Hans Michael Kvasnicka(University Hospital Cologne), Jürgen Thiele(University Hospital Cologne), Ronald Brand(Leiden University Medical Center), Axel R. Zander(Universität Hamburg), Dietger Niederwieser(University Hospital Leipzig), Theo M. de Witte(Radboud University Nijmegen)
Blood
October 7, 2009
Cited by 394Open Access
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Abstract

From 2002 to 2007, 103 patients with primary myelofibrosis or postessential thrombocythemia and polycythemia vera myelofibrosis and a median age of 55 years (range, 32-68 years) were included in a prospective multicenter phase 2 trial to determine efficacy of a busulfan (10 mg/kg)/fludarabine (180 mg/m(2))-based reduced-intensity conditioning regimen followed by allogeneic stem cell transplantation from related (n = 33) or unrelated donors (n = 70). All but 2 patients (2%) showed leukocyte and platelet engraftment after a median of 18 and 22 days, respectively. Acute graft-versus-host disease grade 2 to 4 occurred in 27% and chronic graft-versus-host disease in 43% of the patients. Cumulative incidence of nonrelapse mortality at 1 year was 16% (95% confidence interval, 9%-23%) and significantly lower for patients with a completely matched donor (12% vs 38%; P = .003). The cumulative incidence of relapse at 3 years was 22% (95% confidence interval, 13%-31%) and was influenced by Lille risk profile (low, 14%; intermediate, 22%; and high, 34%; P = .02). The estimated 5-year event-free and overall survival was 51% and 67%, respectively. In a multivariate analysis, age older than 55 years (hazard ratio = 2.70; P = .02) and human leukocyte antigen-mismatched donor (hazard ratio = 3.04; P = .006) remained significant factors for survival. The study was registered at www.clinicaltrials.gov as #NCT 00599547.


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