| Literature DB >> 31730920 |
Suman Paul1, Hua-Ling Tsai1, Patrick Lowery1, Ephraim J Fuchs1, Leo Luznik1, Javier Bolaños-Meade1, Lode J Swinnen1, Satish Shanbhag1, Nina Wagner-Johnston1, Ravi Varadhan1, Richard F Ambinder1, Richard J Jones1, Douglas E Gladstone2.
Abstract
Allogeneic blood or marrow transplantation (allo-BMT) remains the only treatment for chronic lymphocytic leukemia (CLL) with curative potential. Although post-transplantation cyclophosphamide (PTCy) reduces allo-BMT toxicity by decreasing the risk of graft-versus-host disease (GVHD), its effect on CLL allo-BMT outcomes is unknown. We studied 64 consecutive patients with CLL who underwent nonmyeloablative (NMA) haploidentical allo-BMT at Johns Hopkins Sidney Kimmel Comprehensive Cancer Center. In this cohort, the 4-year overall survival was 52% (95% confidence interval [CI], 40% to 68%), and progression-free survival was 37% (95% CI, 26% to 54%). Six patients experienced engraftment failure. PTCy prophylaxis was associated with a modest cumulative incidence of 1-year grade II-IV acute GVHD (27%; %95% CI, 15% to 38%) and %%%2-year chronic GVHD (17%; 95% CI, 7% to 26%). We demonstrate that NMA haploidentical allo-BMT with PTCy is a safe and effective treatment option.Entities:
Keywords: Allogeneic blood or marrow transplantation; Chronic lymphocytic leukemia; Graft-versus-host-disease; Haploidentical; Post-transplantation cyclophosphamide
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Year: 2019 PMID: 31730920 PMCID: PMC9353745 DOI: 10.1016/j.bbmt.2019.11.008
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.609