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,Hengrui Liang,Wenxi Jiang,Wei Wang,Ke Xu,Weipeng Cai,Kui Wu,Antoon Lerut,Junhui Fu,Jianxing He
出处
期刊:International Journal of Cancer [Wiley]
卷期号:151 (1): 128-137 被引量:86
标识
DOI:10.1002/ijc.33976
摘要

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/m2 in total on day 1 and day 8) and cisplatin (75 mg/m2 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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