| Literature DB >> 31498883 |
Ali Bazarbachi1, Ariane Boumendil2, Hervé Finel2, Luca Castagna3, Alida Dominietto4, Didier Blaise5, Jose L Diez-Martin6, Johanna Tischer7, Zafer Gülbas8, Hélène L Wallet9, Lucia L Corral10, Mohamad Mohty11, Yener Koc12, Ibrahim Yakoub-Agha13, Christoph Schmid14, Jean El Cheikh1, Mutlu Arat15, Edouard Forcade16, Peter Dreger17, Vanderson Rocha18, Gonzalo G García19, Yves Chalandon20, Christelle Ferra21, Corentin Orvain22, Stephen Robinson23, Silvia Montoto24, Anna Sureda25.
Abstract
Haploidentical stem cell transplantation (haploSCT) is becoming a major transplant modality for lymphoma. To assess the effects of donor characteristics, stem cell source and conditioning on outcomes, we identified 474 adults with Hodgkin (HL; 240), peripheral T-cell (PTCL; 88), diffuse large B-cell (77), mantle cell (40) or follicular lymphoma (FL; 29), who received haploSCT with post-transplant cyclophosphamide. Median follow-up of alive patients was 32 months. On multivariate analysis, acute graft-versus-host disease (GVHD) grade 2-4 was lower with offspring donors or bone marrow cells, whereas extensive chronic GVHD was higher in partial response at haploSCT or when using sisters, haploidentical donors beyond first degree, or female donors in male patients. Progression-free survival (PFS) was better for FL, HL and PTCL, whereas overall survival (OS) was better for HL and PTCL. Complete remission at haploSCT improved PFS and OS whereas these were negatively affected by cytomegalovirus donor positive/recipient positive status. No other donor characteristics (age, gender, human leucocyte antigen mismatch, ABO incompatibility) affected PFS or OS except use of haploidentical donors beyond first degree, which negatively affected OS. PFS and OS are mostly influenced by disease status and lymphoma subtype, supporting the use of any first degree haploidentical family member as a donor.Entities:
Keywords: conditioning; donor type; haploidentical transplant; lymphoma; stem cell source
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Year: 2019 PMID: 31498883 DOI: 10.1111/bjh.16182
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998