| Literature DB >> 28366766 |
Chengcheng Zhang1, Zhe Wang2, Zhi Yang3, Meiling Wang3, Shiqi Li3, Yunyan Li3, Rui Zhang3, Zhouxing Xiong3, Zhihao Wei3, Junjie Shen3, Yongli Luo3, Qianzhen Zhang3, Limei Liu4, Hong Qin5, Wei Liu6, Feng Wu7, Wei Chen8, Feng Pan2, Xianquan Zhang5, Ping Bie6, Houjie Liang9, Gabriele Pecher10, Cheng Qian11.
Abstract
Chimeric antigen receptor T (CAR-T) cells have shown promising efficacy in treatment of hematological malignancies, but its applications in solid tumors need further exploration. In this study, we investigated CAR-T therapy targeting carcino-embryonic antigen (CEA)-positive colorectal cancer (CRC) patients with metastases to evaluate its safety and efficacy. Five escalating dose levels (DLs) (1 × 105 to 1 × 108/CAR+/kg cells) of CAR-T were applied in 10 CRC patients. Our data showed that severe adverse events related to CAR-T therapy were not observed. Of the 10 patients, 7 patients who experienced progressive disease (PD) in previous treatments had stable disease after CAR-T therapy. Two patients remained with stable disease for more than 30 weeks, and two patients showed tumor shrinkage by positron emission tomography (PET)/computed tomography (CT) and MRI analysis, respectively. Decline of serum CEA level was apparent in most patients even in long-term observation. Furthermore, we observed persistence of CAR-T cells in peripheral blood of patients receiving high doses of CAR-T therapy. Importantly, we observed CAR-T cell proliferation especially in patients after a second CAR-T therapy. Taken together, we demonstrated that CEA CAR-T cell therapy was well tolerated in CEA+ CRC patients even in high doses, and some efficacy was observed in most of the treated patients.Entities:
Keywords: CAR-T; CEA; colorectal carcinoma; dose escalating; phase I; safety and efficacy
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Year: 2017 PMID: 28366766 PMCID: PMC5417843 DOI: 10.1016/j.ymthe.2017.03.010
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454