上皮细胞粘附分子
医学
免疫疗法
耐受性
白细胞减少症
临床试验
癌症研究
生物标志物
免疫学
不利影响
毒性
肿瘤科
免疫系统
内科学
抗原
生物
生物化学
作者
Dan Dan Li,Xianling Guo,Kun Yang,Yuening Yang,Weilin Zhou,Yong Huang,Xiao Liang,Jinhua Su,Jiang Lin,Jing Li,Maorong Fu,Haixia He,Jinrong Yang,Shi H,Hanshuo Yang,Aiping Tong,Nianyong Chen,Jian‐Kun Hu,Qing Xu,Yu-Quan Wei
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2023-12-01
卷期号:9 (48)
被引量:46
标识
DOI:10.1126/sciadv.adg9721
摘要
The efficacy of CAR-T cells for solid tumors is unsatisfactory. EpCAM is a biomarker of epithelial tumors, but the clinical feasibility of CAR-T therapy targeting EpCAM is lacking. Here, we report pre- and clinical investigations of EpCAM-CAR-T cells for solid tumors. We demonstrated that EpCAM-CAR-T cells costimulated by Dectin-1 exhibited robust antitumor activity without adverse effects in xenograft mouse models and EpCAM-humanized mice. Notably, in clinical trials for epithelial tumors (NCT02915445), 6 (50%) of the 12 enrolled patients experienced self-remitted grade 1/2 toxicities, 1 patient (8.3%) experienced reversible grade 3 leukopenia, and no higher-grade toxicity reported. Efficacy analysis determined two patients as partial response. Three patients showed >23 months of progression-free survival, among whom one patient experienced 2-year progress-free survival with detectable CAR-T cells 200 days after infusion. These data demonstrate the feasibility and tolerability of EpCAM-CAR-T therapy.
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