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:Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients.
Ray of dawn: Anti-PD-1 immunotherapy enhances the chimeric antigen receptor T-cell therapy in Lymphoma patients.
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CAR-T 细胞疗法联合抗 PD-1 免疫治疗用于淋巴瘤患者具有疗效,最常见的不良反应是发热。
CAR-T 细胞是一种新型过继细胞疗法,已广泛用于治疗淋巴瘤患者。通过减少CAR-T 细胞功能衰竭并增强抗肿瘤活性,免疫检查点阻断可能提高CAR-T 细胞细胞毒性,已显示出良好疗效。
研究人员检索PubMed、Cochrane Library、Embase和Web of Science数据库,收集2012年1月至2022年8月CAR-T 联合PD-1治疗肿瘤患者的研究数据,并于2023年10月更新检索。计算部分缓解率(PR)、完全缓解率(CR)、客观缓解率(ORR)、死亡率及不良反应发生率。
分析5项临床试验中的57例淋巴瘤患者。合并部分缓解率、完全缓解率和总缓解率分别为21%(95% CI 0.06–0.39,I²=0.37%)、27%(95% CI 0.03–0.60,I²=60.43%)和65%(95% CI 0.23–0.98,I²=76.31%)。细胞因子释放综合征、中性粒细胞减少、发热和疲劳的合并发生率估计分别为57%(95% CI 0.08–0.99,I²=85.20%)、47%(95% CI 0.14–0.81,I²=74.17%)、59%(95% CI 0.27–0.89,I²=60.23%)和50%(95% CI 0.13–0.87,I²=73.89%)。
CAR-T 联合抗PD-1免疫治疗淋巴瘤具有疗效,最常见不良反应为发热。注册:研究方案已在PROSPERO注册,编号CRD42022342647。
Chimeric antigen receptor T (CAR-T) cell therapy, a new adoptive cell therapy, has been widely used to treat lymphoma patients. Immune checkpoint blockade may improve the cytotoxicity of CAR-T cells by reducing the failure of CAR-T cells and improving antitumor activity. It has shown promising efficacy. METHOD: We searched PubMed, the Cochrane Library, Embase and Web of Science from January 2012 to August 2022 to find data reporting the results of CAR-T cells therapy combined with PD-1 in tumor patients. An updated search was conducted in October 2023. The partial response rate (PR), complete response rate (CR), objective response rate (ORR), mortality rate, and incidence of adverse reactions were calculated.
We analyzed 57 lymphoma patients from 5 clinical trials. The pooled partial, complete and overall response rates were 21% (95% CI 0.06-0.39, I 2 = 0.37%), 27% (95% CI 0.03-0.60, I 2 = 60.43%) and 65% (95% CI 0.23-0.98, I 2 = 76.31%), respectively. The pooled incidence of cytokine release syndrome, neutropenia, fever, and fatigue was estimated to be 57% (95% CI 0.08-0.99, I 2 = 85.20%), 47% (95% CI 0.14-0.81, I 2 = 74.17%), 59% (95% CI 0.27-0.89, I 2 = 60.23%), and 50% (95% CI 0.13-0.87, I 2 = 73.89%), respectively.
CAR-T-cell therapy combined with anti-PD-1 immunotherapy in the treatment of lymphoma patients has efficacy, and the most common adverse effect is fever. REGISTRATION: The protocol was registered in prospero, with the registration number CRD42022342647.
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