Hematopoietic Stem-Cell Transplantation for Advanced Systemic Mastocytosis
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Published:2014-10-10
Issue:29
Volume:32
Page:3264-3274
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ISSN:0732-183X
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Container-title:Journal of Clinical Oncology
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language:en
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Short-container-title:JCO
Author:
Ustun Celalettin1, Reiter Andreas1, Scott Bart L.1, Nakamura Ryotaro1, Damaj Gandhi1, Kreil Sebastian1, Shanley Ryan1, Hogan William J.1, Perales Miguel-Angel1, Shore Tsiporah1, Baurmann Herrad1, Stuart Robert1, Gruhn Bernd1, Doubek Michael1, Hsu Jack W.1, Tholouli Eleni1, Gromke Tanja1, Godley Lucy A.1, Pagano Livio1, Gilman Andrew1, Wagner Eva Maria1, Shwayder Tor1, Bornhäuser Martin1, Papadopoulos Esperanza B.1, Böhm Alexandra1, Vercellotti Gregory1, Van Lint Maria Teresa1, Schmid Christoph1, Rabitsch Werner1, Pullarkat Vinod1, Legrand Faezeh1, Yakoub-agha Ibrahim1, Saber Wael1, Barrett John1, Hermine Olivier1, Hagglund Hans1, Sperr Wolfgang R.1, Popat Uday1, Alyea Edwin P.1, Devine Steven1, Deeg H. Joachim1, Weisdorf Daniel1, Akin Cem1, Valent Peter1
Affiliation:
1. Celalettin Ustun, Ryan Shanley, Gregory Vercellotti, and Daniel Weisdorf, University of Minnesota, Minneapolis; William J. Hogan, Mayo Clinic, Rochester, MN; Andreas Reiter and Sebastian Kreil, Universitätsmedizin Mannheim, Mannheim; Herrad Baurmann, Stiftung Deutsche Klinik für Diagnostik, Wiesbaden; Bernd Gruhn, Jena University Hospital, Jena; Tanja Gromke, University of Essen, Essen; Eva Maria Wagner, Universitätsmedizin Mainz, Mainz; Martin Bornhäuser, Universitätsklinikum Dresden, Dresden; Christoph...
Abstract
Purpose Advanced systemic mastocytosis (SM), a fatal hematopoietic malignancy characterized by drug resistance, has no standard therapy. The effectiveness of allogeneic hematopoietic stem-cell transplantation (alloHCT) in SM remains unknown. Patients and Methods In a global effort to define the value of HCT in SM, 57 patients with the following subtypes of SM were evaluated: SM associated with clonal hematologic non–mast cell disorders (SM-AHNMD; n = 38), mast cell leukemia (MCL; n = 12), and aggressive SM (ASM; n = 7). Median age of patients was 46 years (range, 11 to 67 years). Donors were HLA-identical (n = 34), unrelated (n = 17), umbilical cord blood (n = 2), HLA-haploidentical (n = 1), or unknown (n = 3). Thirty-six patients received myeloablative conditioning (MAC), and 21 patients received reduced-intensity conditioning (RIC). Results Responses in SM were observed in 40 patients (70%), with complete remission in 16 patients (28%). Twelve patients (21%) had stable disease, and five patients (9%) had primary refractory disease. Overall survival (OS) at 3 years was 57% for all patients, 74% for patients with SM-AHNMD, 43% for those with ASM, and 17% for those with MCL. The strongest risk factor for poor OS was MCL. Survival was also lower in patients receiving RIC compared with MAC and in patients having progression compared with patients having stable disease or response. Conclusion AlloHCT was associated with long-term survival in patients with advanced SM. Although alloHCT may be considered as a viable and potentially curative therapeutic option for advanced SM in the meantime, given that this is a retrospective analysis with no control group, the definitive role of alloHCT will need to be determined by a prospective trial.
Publisher
American Society of Clinical Oncology (ASCO)
Subject
Cancer Research,Oncology
Cited by
147 articles.
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