当前位置: X-MOL 学术Blood Cancer J. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
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
Blood Cancer Journal ( IF 12.9 ) Pub Date : 2024-07-05 , DOI: 10.1038/s41408-024-01085-9
Philipp Berning 1 , Mathilde Fekom 2 , Maud Ngoya 2 , Anthony H Goldstone 3 , Peter Dreger 4 , Silvia Montoto 5 , Hervé Finel 2 , Evgenii Shumilov 1 , Patrice Chevallier 6 , Didier Blaise 7 , Tim Strüssmann 8 , Ben Carpenter 9 , Edouard Forcade 10 , Cristina Castilla-Llorente 11 , Marek Trneny 12 , Hervé Ghesquieres 13 , Saveria Capria 14 , Catherine Thieblemont 15 , Igor Wolfgang Blau 16 , Ellen Meijer 17 , Annoek E C Broers 18 , Anne Huynh 19 , Denis Caillot 20 , Wolf Rösler 21 , Stephanie Nguyen Quoc 22 , Jörg Bittenbring 23 , Arnon Nagler 24 , Jacques-Emmanuel Galimard 2 , Bertram Glass 25 , Anna Sureda 26 , Norbert Schmitz 1
Affiliation  

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.



中文翻译:


造血干细胞移植治疗 DLBCL:欧洲血液和骨髓移植协会 32 年来对 40,000 多名患者的报告



自体(auto-)和同种异体(allo-)造血干细胞移植(HSCT)是复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)的关键治疗方法,尽管它们的作用受到CAR-T细胞和其他免疫疗法的挑战。我们检查了 1990 年至 2021 年间向 EBMT 报告的接受自体/异体 HSCT 的 DLBCL 患者的移植趋势和结果。在此期间,有 41,148 例患者接受了自体 HSCT,在 2016 年达到峰值 1911 例,而同种异体 HSCT 在 2018 年最多达到 294 例。近期移植数量的下降与 CAR-T 治疗的增加相对应(2021 年为 1117 例)。自体造血干细胞移植的中位年龄从42岁(1990-1994年)上升到58岁(2015-2021年),1994年后外周血成为主要干细胞来源。 Allo-HSCT的中位年龄从36岁(1990-1994年)增加到54岁(2015-2021年),1998年后以动员血液为主要来源,2000年后降低了强度调节。 2015-2021年,不相关和不匹配的allo-HSCT分别占allo-HSCT的50%和19%。自体 HSCT 后三年总生存率 (OS) 从 56% (1990-1994) 提高到 70% (2015-2021), p < 0.001,复发率 (RI) 从 49% 下降到 38%,而非复发死亡率(NRM)保持不变(4%)。 allo-HSCT 后,3 年 OS 率从 33% (1990-1999) 增加到 46% (2015-2021) ( p < 0.001); 3 年 RI 保持在 39%,1 年 NRM 下降至 19% ( p < 0.001)。我们的数据反映了 32 年来的进步和超过 40,000 例移植手术,为评估新兴 DLBCL 疗法提供了见解。

更新日期:2024-07-05
down
wechat
bug