| Literature DB >> 23380340 |
Mehdi Hamadani1, Wael Saber, Kwang Woo Ahn, Jeanette Carreras, Mitchell S Cairo, Timothy S Fenske, Robert Peter Gale, John Gibson, Gregory A Hale, Parameswaran N Hari, Jack W Hsu, David J Inwards, Rammurti T Kamble, Anderas Klein, Dipnarine Maharaj, David I Marks, David A Rizzieri, Bipin N Savani, Harry C Schouten, Edmund K Waller, Baldeep Wirk, Ginna G Laport, Silvia Montoto, David G Maloney, Hillard M Lazarus.
Abstract
Patients with chemorefractory non-Hodgkin lymphomas generally have a poor prognosis. We used the observational database of the Center for International Blood and Marrow Transplant Research to study the outcome of 533 patients with refractory diffuse large B cell lymphoma (DLBCL) or grade III follicular lymphoma (FL-III) who underwent allogeneic hematopoietic cell transplantation (allo-HCT) using either myeloablative (MA; n = 307) or reduced-intensity/nonmyeloablative conditioning (RIC/NST; n = 226) between 1998 and 2010. We analyzed nonrelapse mortality (NRM), relapse/progression, progression-free survival (PFS), and overall survival (OS). Only 45% of the patients at transplantation had a Karnofsky performance score of ≥90%. Median follow-up of surviving patients after MA and RIC/NST allo-HCT is 35 months and 30 months, respectively. At 3 years, MA allo-HCT was associated with a higher NRM compared with RIC/NST (53% versus 42%; P = .03), similar PFS (19% versus 23%; P = .40), and lower OS (19% versus 28%; P = .02), respectively. On multivariate analysis, FL-III histology was associated with lower NRM (relative risk [RR], .52), reduced risk of relapse/progression (RR, .42), and superior PFS (RR, .51) and OS (RR, .53), whereas MA conditioning was associated with reduced risk of relapse/progression (RR, .66). Despite a refractory state, a small subset of DLBCL and FL-III patients can attain durable remissions after allo-HCT. Conditioning regimen intensity was not associated with PFS and OS despite a higher risk of relapse/progression with RIC/NST allo-HCT.Entities:
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Year: 2013 PMID: 23380340 PMCID: PMC3650915 DOI: 10.1016/j.bbmt.2013.01.024
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742