Back to Search Start Over

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.

Authors :
Berning, Philipp
Fekom, Mathilde
Ngoya, Maud
Goldstone, Anthony H.
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
Source :
Blood Cancer Journal; 7/5/2024, Vol. 14 Issue 1, p1-13, 13p
Publication Year :
2024

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20445385
Volume :
14
Issue :
1
Database :
Complementary Index
Journal :
Blood Cancer Journal
Publication Type :
Academic Journal
Accession number :
178295171
Full Text :
https://doi.org/10.1038/s41408-024-01085-9