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:Comparative effectiveness of chimeric antigen receptor (CAR) T-cell therapy versus historical controls in patients with relapse/refractory aggressive B-cell lymphoma: An indirect treatment comparison in the real-world setting.
Comparative effectiveness of chimeric antigen receptor (CAR) T-cell therapy versus historical controls in patients with relapse/refractory aggressive B-cell lymphoma: An indirect treatment comparison in the real-world setting.
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单臂研究显示,复发/难治性(R/R)侵袭性B细胞淋巴瘤患者接受治疗后生存显著改善,但同时存在显著毒性且成本极高。本研究旨在评估加拿大安大略省公共资助的嵌合抗原受体(CAR)T细胞疗法治疗侵袭性B细胞淋巴瘤患者的真实世界健康结局,并与历史对照比较。
我们开展基于人群的回顾性队列研究,纳入2013年1月至2023年6月在安大略省接受R/R侵袭性B细胞淋巴瘤治疗的患者。队列包括2019年1月1日至2023年6月30日期间接受商业化CAR-T 细胞治疗的患者,以及2013年1月1日至2018年12月31日期间、CAR-T 治疗尚未获得公共资助时接受标准治疗的历史对照。采用逆概率治疗加权(IPTW)平衡两组患者特征。队列包括314例CAR-T 细胞治疗患者和106例历史对照。中位随访时间为29.6个月(95%置信区间[CI]:26.1–33.0);CAR-T 治疗患者和历史对照的中位总生存期分别为15.1个月(95% CI:11.1–26.3)和4.8个月(95% CI:3.8–6.4),风险比为0.50(95% CI:0.38–0.65)。这些结果支持CAR-T 细胞治疗在常规临床照护中有益于R/R侵袭性B细胞淋巴瘤患者。
Single-arm studies demonstrate dramatic improvements in survival in patients with relapsed/refractory (R/R) aggressive B-cell lymphomas but with significant toxicities and at exceptionally high costs. The objective of this study was to evaluate the real-world health outcomes of aggressive B-cell lymphoma patients treated with publicly funded chimeric antigen receptor (CAR) T-cell therapy in Ontario, Canada, compared to historical controls.
We conducted a population-based retrospective cohort study among patients treated for R/R aggressive B-cell lymphoma in Ontario between January 2013 and June 2023. The cohort consisted of patients who received commercially available CAR T cells between 1 January 2019 and 30 June 2023 and historical controls who were treated with the standard of care between 1 January 2013 and 31 December 2018, before public funding for CAR T-cell treatments was available. Inverse probability of treatment weighting (IPTW) was used to balance patients' characteristics across the two groups.
The cohort included 314 CAR T-cell patients and 106 historical controls. The median follow-up time was 29. 6 months (95% confidence interval [CI]: 26. 1-33. 0), and the median overall survival was 15. 1 months (95% CI, 11. 1-26. 3) and 4. 8 months (95% CI, 3. 8-6. 4) for CAR T-cell-treated patients and historical controls (hazard ratio 0. 50, 95% CI 0. 38-0. 65) respectively. These results support the benefit of CAR T-cell treatment for patients with R/R aggressive B-cell lymphoma in routine clinical care.
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