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瑞士的造血细胞移植和细胞治疗:25 年演变——来自 SBST 1997-2021 干细胞移植和细胞治疗工作组的报告

英文原题:Hematopoietic cell transplantation and cellular therapies in Switzerland. Evolution over 25 years. A report from the stem cell transplantation and cellular therapies working groups of the SBST 1997-2021.

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Hematopoietic cell transplantation and cellular therapies in Switzerland. Evolution over 25 years. A report from the stem cell transplantation and cellular therapies working groups of the SBST 1997-2021.

PubMed 2023/12/06(内容时间) Hematol Oncol Q1 · IF 4.1(JCR 2025)

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中文摘要

瑞士血液干细胞移植和细胞治疗组(SBST)负责管理全国强制性造血细胞移植(HCT)及细胞治疗登记系统。历经25年,已有11,226名HCT患者资料,包括4,031例异基因移植、7,195例自体移植及925名儿童。研究按五年时期(1997–2001、2002–2006、2007–2011、2012–2016和2017–2021)比较患者特征及结局,发现多个方面随时间改变。异基因移植受者年龄增大(中位年龄33.7岁升至54.3岁),后期更常使用非亲缘供者和减低强度预处理。自体HCT受者年龄也上升(中位48.3岁升至59.9岁)。SARS-CoV-2疫情期间移植活动未显著下降。

调整危险因素后,与首个五年期相比,最近五年期总生存期改善(死亡相对风险[RR]0.664,95% CI 0.529–0.832),无进展生存期也改善(RR 0.708,95% CI 0.577–0.870)。异基因HCT非复发死亡率随时间下降(RR 0.371,95% CI 0.270–0.509),但复发风险未下降。自体HCT结局也随时间改善,主要归因于复发风险降低(RR 0.681,95% CI 0.597–0.777),可能与维持治疗或骨髓瘤患者复发后的挽救治疗有关。2019年瑞士批准首个商业化CAR-T 产品后,异基因或自体HCT以外的细胞治疗,尤其CAR-T,开始增加;但目前CAR-T 数据尚不足以进行比较分析。

本研究详细分析了各时期变化。该研究涵盖所有HCT及细胞治疗,可用于质量保证、医疗成本估算和基准比较。两类HCT后均有50%至60%患者长期生存,提示需要长期照护的幸存者群体不断扩大。

展开英文摘要原文

The Swiss Blood Stem Cell Transplantation and Cellular Therapy Group (SBST) leads a mandatory national registry for all hematopoietic stem cell transplants (HCT) and cellular therapies. After 25 years, information was available for 11,226 patients receiving an HCT (4031 allogeneic and 7195 autologous), including 925 pediatric patients.

We compared patient characteristics and outcome by quinquennia 1997-2001, 2002-2006, 2007-2011, 2012-2016, and 2017-2021. There were numerous changes over time. Allogeneic transplant recipients became older (median age 33. 7 vs. 54. 3) and had more frequently unrelated donors and reduced intensity conditioning in later quinquennia. Similarly, age increased for recipients of autologous HCT (median 48. 3 vs. 59. 9).

We did not see a significant drop in transplant activity during the SARS-CoV-2 pandemic. Analysis of outcome showed overall survival (relative risk (RR) of death 0. 664 (0. 529-0. 832) and progression free survival (RR 0. 708 (0. 577-0. 870) being improved over time comparing the latest to the first quinquennium adjusting for risk factors. Non-relapse mortality decreased in recipients of allogeneic HCT (RR: 0. 371 (0. 270-0. 509)) over time but relapse risks did not. Outcome of autologous HCT improved as well across quinquennia, this improvement was mainly due to decreased relapse risks (RR 0.

681 (0. 597-0. 777)), possibly related to maintenance treatment or rescue treatment for relapse mainly in myeloma patients. Cellular therapies other than allogeneic or autologous HCT, particularly chimeric antigen receptor T-cells (CAR-T) treatment have started to increase after 2019, year of approval of the first commercial CAR-T product in Switzerland. Data on chimeric antigen receptor T-cell treatment are too early for comparative analyses. Detailed analyses of changes over time are presented.

This study includes all HCTs, and cellular therapies, data useful for quality assurance programs, health care cost estimation and benchmarking. Between 50% and 60% of patients are long-term survivors after both types of HCT, indicating growing populations of surviving patients requiring long-term care.

论文信息

作者
Passweg JR、Baldomero H、Ansari M、Arber C、Chalandon Y、Daskalakis M、Diepold M、Diesch-Furlanetto T
单位
Hematology Division and Pediatric Hematology-oncology University Hospital and Children's University Hospital, Basel, Switzerland.Switzerland
期刊
Hematological oncology2024 Jan
原文标识
PubMed 38058031 · DOI 10.1002/hon.3241