Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/214889
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dc.contributor.authorBerning, Philipp-
dc.contributor.authorFekom, Mathilde-
dc.contributor.authorNgoya, Maud-
dc.contributor.authorGoldstone, Anthony H.-
dc.contributor.authorDreger, Peter-
dc.contributor.authorMontoto, Silvia-
dc.contributor.authorFinel, Hervé-
dc.contributor.authorShumilov, Evgenii-
dc.contributor.authorChevallier, Patrice-
dc.contributor.authorBlaise, Didier-
dc.contributor.authorStrüssmann, Tim-
dc.contributor.authorCarpenter, Ben-
dc.contributor.authorForcade, Edouard-
dc.contributor.authorCastilla Llorente, Cristina-
dc.contributor.authorTrneny, Marek-
dc.contributor.authorGhesquieres, Hervé-
dc.contributor.authorCapria, Saveria-
dc.contributor.authorThieblemont, Catherine-
dc.contributor.authorBlau, Igor Wolfgang-
dc.contributor.authorMeijer, Ellen-
dc.contributor.authorBroers, Annoek E. C.-
dc.contributor.authorHuynh, Anne-
dc.contributor.authorCaillot, Denis-
dc.contributor.authorRösler, Wolf-
dc.contributor.authorNguyen Quoc, Stephanie-
dc.contributor.authorBittenbring, Jörg-
dc.contributor.authorNagler, Arnon-
dc.contributor.authorGalimard, Jacques Emmanuel-
dc.contributor.authorGlass, Bertram-
dc.contributor.authorSureda, Anna-
dc.contributor.authorSchmitz, Norbert-
dc.date.accessioned2024-08-30T14:58:43Z-
dc.date.available2024-08-30T14:58:43Z-
dc.date.issued2024-07-05-
dc.identifier.issn2044-5385-
dc.identifier.urihttps://hdl.handle.net/2445/214889-
dc.description.abstractAutologous(auto-) and allogeneic(allo-) hematopoietic stem cell transplantation (HSCT) are key treatments for relapsed/refractory diffuse large B-cell lymphoma (DLBCL), although their roles are challenged by CAR-T-cells and other immunotherapies. We examined the transplantation trends and outcomes for DLBCL patients undergoing auto-/allo-HSCT between 1990 and 2021 reported to EBMT. Over this period, 41,148 patients underwent auto-HSCT, peaking at 1911 cases in 2016, while allo-HSCT saw a maximum of 294 cases in 2018. The recent decline in transplants corresponds to increased CAR-T treatments (1117 cases in 2021). Median age for auto-HSCT rose from 42 (1990-1994) to 58 years (2015-2021), with peripheral blood becoming the primary stem cell source post-1994. Allo-HSCT median age increased from 36 (1990-1994) to 54 (2015-2021) years, with mobilized blood as the primary source post-1998 and reduced intensity conditioning post-2000. Unrelated and mismatched allo-HSCT accounted for 50% and 19% of allo-HSCT in 2015-2021. Three-year overall survival (OS) after auto-HSCT improved from 56% (1990-1994) to 70% (2015-2021), p < 0.001, with a decrease in relapse incidence (RI) from 49% to 38%, while non-relapse mortality (NRM) remained unchanged (4%). After allo-HSCT, 3-year-OS increased from 33% (1990-1999) to 46% (2015-2021) (p < 0.001); 3-year RI remained at 39% and 1-year-NRM decreased to 19% (p < 0.001). Our data reflect advancements over 32 years and >40,000 transplants, providing insights for evaluating emerging DLBCL therapies.-
dc.format.extent13 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Science and Business Media LLC-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41408-024-01085-9-
dc.relation.ispartofBlood Cancer Journal, 2024, vol. 14, num. 1-
dc.relation.urihttps://doi.org/10.1038/s41408-024-01085-9-
dc.rightscc by (c) Berning, Philipp et al, 2023-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationCèl·lules mare-
dc.subject.classificationTrasplantament d'òrgans-
dc.subject.otherStem cells-
dc.subject.otherTransplantation of organs-
dc.titleHematopoietic stem cell transplantation for DLBCL: a report from the European Society for Blood and Marrow Transplantation on more than 40,000 patients over 32 years-
dc.typeinfo:eu-repo/semantics/article-
dc.typenfo:eu-repo/semantics/publishedVersion-
dc.date.updated2024-07-30T09:49:10Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid38969655-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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