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

被引:111
|
作者
Liu, Jun [1 ,2 ]
Li, Jingpei [1 ,2 ]
Lin, Wanli [3 ]
Shao, Di [4 ]
Depypere, Lieven [5 ,6 ]
Zhang, Zhifeng [7 ]
Li, Zhuoyi [1 ,2 ]
Cui, Fei [1 ,2 ]
Du, Zesen [8 ]
Zeng, Yuan [1 ,2 ]
Jiang, Shunjun [9 ]
He, Ping [10 ]
Gu, Xia [10 ]
Chen, Huai [11 ]
Zhang, Hai [3 ]
Lin, Xiaowei [7 ]
Huang, Haoda [7 ]
Lv, Wenqiang [7 ]
Cai, Weiming [7 ]
Liang, Wenhua [1 ,2 ]
Liang, Hengrui [1 ,2 ]
Jiang, Wenxi [4 ]
Wang, Wei [1 ,2 ]
Xu, Ke [1 ,2 ]
Cai, Weipeng [1 ,2 ]
Wu, Kui [4 ]
Lerut, Toni [5 ,6 ]
Fu, Junhui [1 ,2 ,8 ]
He, Jianxing [1 ,2 ]
机构
[1] Guangzhou Med Univ, Dept Thorac Surg, Affiliated Hosp 1, Guangzhou, Peoples R China
[2] Guangzhou Med Univ, Guangzhou Inst Resp Dis, Guangzhou Inst Resp Hlth, State Key Lab Resp Dis,Affiliated Hosp 1, Guangzhou, Peoples R China
[3] Peoples Hosp Gaozhou, Dept Thorac Surg, Gaozhou, Peoples R China
[4] BGI Shenzhen, BGI Genom, Shenzhen, Peoples R China
[5] Univ Hosp Leuven, Dept Thorac Surg, Leuven, Belgium
[6] Katholieke Univ Leuven, Lab Resp Dis & Thorac Surg BREATHE, Dept Chron Dis & Metab CHROMETA, Leuven, Belgium
[7] Peoples Hosp Jieyang, Dept Thorac Surg, Jieyang, Peoples R China
[8] Shantou Cent Hosp, Dept Surg Oncol, Shantou, Peoples R China
[9] Guangzhou Med Univ, Dept Phamarcol, Affiliated Hosp 1, Guangzhou, Peoples R China
[10] Guangzhou Med Univ, Dept Pathol, Affiliated Hosp 1, Guangzhou, Peoples R China
[11] Guangzhou Med Univ, Dept Radiog, Affiliated Hosp 1, Guangzhou, Peoples R China
关键词
camrelizumab; esophageal squamous cell carcinoma; locally advanced; neoadjuvant chemoimmunotherapy; resectable; CHEMORADIOTHERAPY; SURGERY; CANCER; TRIAL; RECURRENCE; PATTERNS;
D O I
10.1002/ijc.33976
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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/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.
引用
收藏
页码:128 / 137
页数:10
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