CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Real-world experience among patients with relapsed/refractory mantle cell lymphoma after Bruton tyrosine kinase inhibitor failure in Europe: The SCHOLAR-2 retrospective chart review study.
Real-world experience among patients with relapsed/refractory mantle cell lymphoma after Bruton tyrosine kinase inhibitor failure in Europe: The SCHOLAR-2 retrospective chart review study.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
复发性套细胞淋巴瘤(MCL)预后较差。目前尚无标准治疗方案,且可用的治疗证据有限,尤其是在Bruton酪氨酸激酶抑制剂(BTKi)治疗失败的患者中。这项多中心回顾性病历审查研究SCHOLAR-2填补了这一知识空白,报告了从240例欧洲复发/难治性MCL患者中收集的数据,这些患者在2012年7月至2018年7月期间接受了基于BTKi的治疗,并在BTKi治疗期间出现疾病进展或因不耐受而停用BTKi治疗。从首次BTKi治疗开始计算,总体队列的中位总生存期(OS)为14.6个月(95%置信区间[CI] 11.6-20.0),91例未接受BTKi后治疗的患者为5.5个月(95% CI 3.9-8.2),149例接受了BTKi后治疗(不包括CAR-T 细胞治疗)的患者为23.8个月(95% CI 18.9-30.1)。在后一组中,患者接受BTKi后治疗的中位线数为一线(范围,一至七线),其中含来那度胺的方案和苯达莫司汀联合利妥昔单抗是最常使用的方案;从首次BTKi后治疗开始计算的中位OS为9.7个月(95% CI 6.3-12.7)。这些结果为BTKi治疗失败后接受挽救治疗的R/R MCL患者的生存提供了基准。
Mantle cell lymphoma (MCL) after relapse is associated with poor prognosis. No standard of care exists and available evidence for treatments is limited, particularly in patients who fail Bruton tyrosine kinase inhibitor (BTKi) therapy. This multicentre retrospective chart review study, SCHOLAR-2, addresses this knowledge gap and reports on data collected from 240 patients with relapsed/refractory MCL in Europe who were treated with BTKi-based therapy between July 2012 and July 2018, and had experienced disease progression while on BTKi therapy or discontinued BTKi therapy due to intolerance. The median overall survival (OS) from initiation of first BTKi therapy was 14.
6 months (95% confidence interval [CI] 11. 6-20. 0) in the overall cohort, 5. 5 months (95% CI 3. 9-8. 2) in 91 patients without post-BTKi therapy, and 23. 8 months (95% CI 18. 9-30. 1) in 149 patients who received post-BTKi therapy (excluding chimeric antigen receptor T-cell treatment).
In the latter group, patients received a median of one (range, one to seven) line of post-BTKi therapy, with lenalidomide-containing regimens and bendamustine plus rituximab being the most frequently administered; the median OS from initiation of first post-BTKi therapy was 9. 7 months (95% CI 6. 3-12. 7). These results provide a benchmark for survival in patients with R/R MCL receiving salvage therapy after BTKi failure.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。