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Neoadjuvant camrelizumab plus chemotherapy for resectable, locally advanced esophageal squamous cell carcinoma (NIC‐ESCC2019): A multicenter, phase 2 study

医学 食管鳞状细胞癌 新辅助治疗 内科学 肿瘤科 化疗 基底细胞 临床研究阶段 多中心研究 食道疾病 外科 食管 癌症 随机对照试验 乳腺癌
作者
Jun Liu,Jingpei Li,Wanli Lin,Ди Шао,Lieven Depypere,Zhifeng Zhang,Zhuoyi Li,Fei Cui,Ze-Sen Du,Yuan Zeng,Shunjun Jiang,Ping He,Xia Gu,Huai Chen,Hai Zhang,Xiaowei Lin,Haoda Huang,Wenqiang Lv,Wei-Ming Cai,Wenhua Liang
出处
期刊:International Journal of Cancer [Wiley]
卷期号:151 (1): 128-137 被引量:143
标识
DOI:10.1002/ijc.33976
摘要

Abstract Optimal treatment for resectable esophageal squamous cell carcinoma (ESCC) is controversial, especially in the context of potential benefit of combining PD‐1 blockade with neoadjuvant therapy. This phase 2 study aimed to assess neoadjuvant camrelizumab plus chemotherapy in this population. Patients (clinical stage II‐IVA) received two cycles of neoadjuvant chemoimmunotherapy (NIC) with camrelizumab (200 mg on day 1) plus nab‐paclitaxel (260 mg/m 2 in total on day 1 and day 8) and cisplatin (75 mg/m 2 in total on days 1‐3) of each 21‐day cycle. Surgery was performed approximately 6 weeks after completion of NIC. Primary endpoint was complete pathologic response (CPR) rate in primary tumor. Secondary endpoints were objective response rate (ORR) per RECIST v1.1, 2‐year progression‐free survival (PFS) rate after surgery, PFS, overall survival (OS) and safety during NIC and perioperative period. Between 17 January 2020 and 8 December 2020, 56 patients were enrolled, and 51 received esophagectomy. Data cutoff date was 25 August 2021. The CPR rate was 35.3% (95% CI, 21.7%‐48.9%). NIC had an ORR of 66.7% (95% CI, 40.0%‐70.4%) and treatment‐related adverse events (TRAEs) of low severity (grade 1‐2, 75.0%; grade 3, 10.7%; grade 4‐5, no). No perioperative mortality occurred. Three (5.9%) patients had tumor recurrence and one (2.0%) patient died. The 2‐year PFS rate, median PFS and median OS had not been reached yet. Camrelizumab plus neoadjuvant chemotherapy in resectable ESCC demonstrates promising efficacy with acceptable toxicity, providing a feasible and effective option. Study is ongoing for long‐term survival analyses.
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