Hematopoietic 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

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Berning, Philipp | Fekom, Mathilde | Ngoya, Maud | Goldstone, Anthony | Dreger, Peter | Montoto, Silvia | Finel, Hervé | Shumilov, Evgenii | Chevallier, Patrice | Blaise, Didier | Strüssmann, Tim | Carpenter, Ben | Forcade, Edouard | Castilla-Llorente, Cristina | Trneny, Marek | Ghesquieres, Hervé | Capria, Saveria | Thieblemont, Catherine | Blau, Igor Wolfgang | Meijer, Ellen | Broers, Annoek | Huynh, Anne | Caillot, Denis | Rösler, Wolf | Nguyen Quoc, Stephanie | Bittenbring, Jörg | Nagler, Arnon | Galimard, Jacques-Emmanuel | Glass, Bertram | Sureda, Anna | Schmitz, Norbert

Edité par CCSD ; Nature Publishing Group -

International audience. Abstract Autologous(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.

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