决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:CAR-T Cell Therapy for Solid Tumors: Are we Still That Far? a Systematic Review of Literature.
纳入29项前瞻性研究(265例患者)。
本系统综述旨在评估迄今为止发表的所有关于CAR-T细胞疗法在实体瘤中疗效的前瞻性研究。检索的数据库为PubMed和Google Scholar,检索时间从建库至2021年5月1日。检索式为(嵌合抗原受体)或(CAR-T)或(T-CAR)。共纳入29项前瞻性研究(265例患者)。大多数已发表的临床试验为I期。临床获益在上皮性卵巢癌中为100%,胃肠道肿瘤中为70-82%,间皮瘤中为79%,小细胞肺癌中为63%,肉瘤中为24-67%,前列腺癌中为50-62%,中枢神经系统肿瘤中为45-50%。未观察到严重的CAR-T细胞特异性严重毒性。
This systematic review aims to assess all the prospective studies published to date on the efficacy of CAR-T cell therapy in solid tumors. Databases searched were PubMed and Google Scholar from inception through May 1st 2021. Search query was (Chimeric antigen receptor) or (CAR-T) or (T-CAR). Twenty-nine prospective studies (265 patients) were included. Most published clinical trials are phase I. Clinical benefit was 100% in epithelial ovarian cancer, 70-82% in gastrointestinal tumors, 79% in mesothelioma, 63% in small-cell lung cancer, 24-67% in sarcoma, 50-62% in prostate cancer, and 45-50% in central nervous system tumors. No serious CAR-T cell specific serious toxicities were noted.
MEMBER ACCOUNT
登录成功会直接打开下一页。