| Literature DB >> 29728701 |
Peter Dreger1,2,3, Mauricette Michallet4, Paul Bosman5, Sascha Dietrich6,7, Mohamad Sobh4, Ariane Boumendil6, Arnon Nagler8, Christof Scheid9, Jan Cornelissen10, Dietger Niederwieser11, Lutz Müller12, Elizabeth Vandenberghe13, Ilaria Scortechini14, Helene Schoemans15, Niels S Andersen16, Jürgen Finke17, Domenico Russo18, Per Ljungman19, Jakob Passweg20, Michel van Gelder5,21, Nadira Durakovic22, Helene Labussiere-Wallet23, Tobias Berg24, Gerald Wulf25, Wolfgang Bethge26, Donald Bunjes27, Stefan Stilgenbauer27, Maria Elisa Canepari28, Michel Schaap29, Christopher P Fox30, Nicolaus Kröger5,31, Silvia Montoto6,32, Johannes Schetelig5,33.
Abstract
The aim of this retrospective study was to investigate the safety and efficacy of allogeneic hematopoietic cell transplantation (alloHCT) in patients pre-treated with ibrutinib. Eligible were patients aged >18 years allotransplanted for chronic lymphocytic leukemia (CLL) or mantle cell lymphoma (MCL) after prior exposure to ibrutinib who were registered with the EBMT registry. Seventy patients (CLL 48, MCL 22) were included. At the time of alloHCT, 73% of the patients were ibrutinib responsive. All patients except one engrafted, and acute GVHD grade 2-4 (3-4) was observed in 49% (12%) of 68 evaluable patients. The cumulative incidence of chronic GVHD was 54% 1 year after transplant. In the CLL group, 12-month non-relapse mortality, relapse incidence (RI), progression-free survival (PFS), and overall survival (OS) were 10, 30, 60, and 72%, respectively, and in the MCL group 5, 19, 76, and 86%, respectively. Pre-transplant ibrutinib failure and poor performance status predicted inferior RI, PFS and OS in the CLL group. In conclusion, ibrutinib does not affect the safety of a subsequent alloHCT. While the relatively high post-transplant relapse risk in ibrutinib-exposed patients with CLL deserves further study, in patients with MCL consolidating disease responses to ibrutinib with alloHCT seems to be a promising option.Entities:
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Year: 2018 PMID: 29728701 DOI: 10.1038/s41409-018-0207-4
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483