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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
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.
Real-World Eligibility for Second-Line Chimeric Antigen Receptor T Cell Therapy in Large B Cell Lymphoma: A Population-Based Analysis.
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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。
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.
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