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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

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

摘要

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.