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大 B 细胞淋巴瘤二线 CAR-T 细胞治疗的真实世界合格性:基于人群的分析

英文原题:Real-World Eligibility for Second-Line Chimeric Antigen Receptor T Cell Therapy in Large B Cell Lymphoma: A Population-Based Analysis.

查看英文原题

Real-World Eligibility for Second-Line Chimeric Antigen Receptor T Cell Therapy in Large B Cell Lymphoma: A Population-Based Analysis.

PubMed 2022/02/02(内容时间) Transplant Cell Ther Q1 · IF 4.7(JCR 2025)

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中文摘要

ZUMA-7 试验证明,对于复发/难治性(r/r)大 B 细胞淋巴瘤(LBCL),二线嵌合抗原受体(CAR)T 细胞疗法优于伴或不伴自体干细胞移植(ASCT)的标准治疗化疗。

我们进行了一项基于人群的回顾性分析,以确定真实世界环境中适合接受二线 CAR-T 细胞治疗的患者。在 2015 年至 2019 年间的 125 例 r/r LBCL 患者中,82% 在一线化学免疫治疗(CIT)后 12 个月内进展,40% 接受了意向性移植治疗,22% 接受了 ASCT,7% 在 ASCT 后获得持久缓解。中位随访时间为 2.8 年,所有患者的中位总生存期(OS)为 5.1 个月,3 年 OS 为 15%(95% 置信区间 [CI],7% 至 20%);在 CIT 后 12 个月内进展的患者中,中位 OS 为 5.1 个月,3 年 OS 为 10%(95% CI,5% 至 17%)。尽管只有 14% 的患者符合 ZUMA-7 研究的所有纳入标准,但多达 65% 在 CIT 后 12 个月内进展的患者具有足够的体能状态,可被认为可能适合接受二线 CAR-T 细胞治疗。虽然当前的标准治疗对大多数 r/r LBCL 患者预后不佳,但在二线治疗中使用 CAR-T 细胞疗法可大幅增加在 LBCL 首次进展时能够接受治愈性意向治疗的患者比例。

展开英文摘要原文

The ZUMA-7 trial demonstrated the superiority of second-line chimeric antigen receptor (CAR) T cell therapy over standard of care chemotherapy with or without autologous stem cell transplantation (ASCT) for relapsed/refractory (r/r) large B cell lymphoma (LBCL).

We conducted a retrospective population-based analysis to determine eligibility for second-line CAR-T cell therapy in the real-world setting. Among 125 patients with r/r LBCL between 2015 and 2019, 82% progressed within 12 months of first-line chemoimmunotherapy (CIT), 40% were treated with intention-to-transplantation, 22% underwent ASCT, and 7% achieved a durable remission after ASCT. With a median follow-up of 2. 8 years, the median overall survival (OS) was 5. 1 months, and 3-year OS was 15% (95% confidence interval [CI], 7% to 20%) for all patients and 10% (95% CI, 5% to 17%) for those progressing within 12 months of CIT.

Although only 14% of patients met all the ZUMA-7 study inclusion criteria, as many as 65% of patients progressing within 12 months of CIT had adequate performance status to be considered potentially eligible for second-line CAR T cell therapy. Whereas the current standard of care results in poor outcomes for most patients with r/r LBCL, the use of CAR T cell therapy in second-line therapy could substantially increase the proportion of patients able to receive curative-intent treatment at first progression of LBCL.

论文信息

作者
Puckrin R、Stewart DA、Shafey M
单位
University of Calgary and Tom Baker Cancer Centre, Calgary, Alberta, Canada. Electronic address: robert.puckrin@ahs.ca.Canada
期刊
Transplantation and cellular therapy2022 Apr
原文标识
PubMed 35123117 · DOI 10.1016/j.jtct.2022.01.024