EpCAM-targeting CAR-T cell immunotherapy is safe and efficacious for epithelial tumors

Author:

Li Dan1ORCID,Guo Xianling2ORCID,Yang Kun3ORCID,Yang Yuening1ORCID,Zhou Weilin1ORCID,Huang Yong1ORCID,Liang Xiao14,Su Jinhua1,Jiang Lin1,Li Jing1,Fu Maorong1,He Haixia156,Yang Jinrong17,Shi Huashan1ORCID,Yang Hanshuo1,Tong Aiping1ORCID,Chen Nianyong4ORCID,Hu Jiankun3ORCID,Xu Qing2ORCID,Wei Yu-Quan1ORCID,Wang Wei1ORCID

Affiliation:

1. Department of Biotherapy, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

2. Department of Oncology, Shanghai Tenth Peoples’ Hospital, Shanghai, China.

3. Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, China.

4. Department of Head and Neck Oncology, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

5. Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Medical Research Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China.

6. Department of Radiation Oncology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.

7. Department of Hematology, Hematology Research Laboratory, West China Hospital, Sichuan University, Chengdu, China.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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