Yang Liu
Yelei Guo
Jingdan Qiu
Zhiqiang Wu
Hanren Dai
Qingming Yang
Yao Wang
Weidong Han
1 Department of Bio-therapeutic, Chinese PLA General Hospital, Beijing 100853, China;
2 Department of Geriatric Hematology, Chinese PLA General Hospital, Beijing 100853, China;
3 Department of Molecular & Immunology, Chinese PLA General Hospital, Beijing 100853, China
Funds: We would like to thank all patients who participated in this trial. This study was supported by the grants from the National Natural Science Foundation of China (Grant No. 81230061 to WDH), the Science and Technology Planning Project of Beijing City (No. Z151100003915076 to WDH), the National Key Research and Development Program of China (Nos. 2016YFC1303501 and 2016YFC1303504 to WDH).
Received Date: 2017-04-17
Rev Recd Date:2017-06-15
Abstract
Abstract
This phase I clinical trial (NCT01935843) is to evaluate the safety, feasibility, and activity of chimeric antigen receptor-engineered T cell (CART) immunotherapy targeting human epidermal growth factor receptor 2 (HER2) in patients with advanced biliary tract cancers (BTCs) and pancreatic cancers (PCs). Eligible patients with HER2-positive (>50%) BTCs and PCs were enrolled in the trial. Well cultured CART-HER2 cells were infused following the conditioning treatment composed of nabpaclitaxel (100-200 mg/m2) and cyclophosphamide (15-35 mg/kg). CAR transgene copy number in the peripheral blood was serially measured to monitor the expansion and persistence of CART-HER2 cells in vivo. Eleven enrolled patients received 1 to 2-cycle CARTHER2 cell infusion (median CAR+ T cell 2.1×106/kg). The conditioning treatment resulted in mild-to-moderate fatigue, nausea/vomiting, myalgia/arthralgia, and lymphopenia. Except one grade-3 acute febrile syndrome and one abnormal elevation of transaminase (>9 ULN), adverse events related to the infusion of CART-HER2 cells were mild-to-moderate. Post-infusion toxicities included one case of reversible severe upper gastrointestinal hemorrhage which occurred in a patient with gastric antrum invaded by metastasis 11 days after the CART-HER2 cell infusion, and 2 cases of grade 1-2 delayed fever, accompanied by the release of C-reactive protein and interleukin-6. All patients were evaluable for assessment of clinical response, among which 1 obtained a 4.5-months partial response and 5 achieved stable disease. The median progression free survival was 4.8 months (range, 1.5-8.3 months). Finally, data from this study demonstrated the safety and feasibility of CART-HER2 immunotherapy, and showed encouraging signals of clinical activity.Keywords: HER2,
CART,
biliary tract cancers,
pancreatic cancers,
clinical trial
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