Tislelizumab combined with chemotherapy as neoadjuvant therapy for surgically resectable esophageal cancer: A prospective, single-arm, phase II study (TD-NICE)

被引:148
作者
Yan, Xiaolong [1 ]
Duan, Hongtao [1 ]
Ni, Yunfeng [1 ]
Zhou, Yongan [1 ]
Wang, Xiaoping [1 ]
Qi, Haini [1 ]
Gong, Li [2 ]
Liu, Honggang [1 ]
Tian, Feng [1 ]
Lu, Qiang [1 ]
Sun, Jianyong [1 ]
Yang, Ende [1 ]
Zhong, Daixing [1 ]
Wang, Tao [1 ]
Huang, Lijun [1 ]
Wang, Jian [1 ]
Wang, Chaoyang [1 ]
Wang, Yuanyong [1 ]
Wan, Zhiyi [3 ]
Lei, Jie [1 ]
Zhao, Jinbo [1 ]
Jiang, Tao [1 ]
机构
[1] AF Mil Med Univ, Tangdu Hosp, Dept Thorac Surg, 1 Xinsi Rd, Xian, Shaanxi, Peoples R China
[2] Air Force Mil Med Univ, Tangdu Hosp, Dept Pathol, 1 Xinsi Rd, Xian, Shaanxi, Peoples R China
[3] Genecast Biotechnol Co Ltd, 88 Danshan Rd, Xidong Chuangrong Bldg,Suite C 131, Wuxi 214104, Jiangsu, Peoples R China
关键词
Chemotherapy; Esophageal cancer; Neoadjuvant therapy; Tislelizumab; PATHOLOGICAL COMPLETE RESPONSE; SQUAMOUS-CELL CARCINOMA; OPEN-LABEL; PERIOPERATIVE CHEMOTHERAPY; PREOPERATIVE CHEMORADIOTHERAPY; PLUS CHEMOTHERAPY; ADENOCARCINOMA; MULTICENTER; CISPLATIN; REGRESSION;
D O I
10.1016/j.ijsu.2022.106680
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Clinical benefit of neoadjuvant immunotherapy in resectable esophageal squamous cell carcinoma (ESCC). remains unclear. This study evaluated the efficacy and safety of the programmed death 1 (PD-1) inhibitor tislelizumab combined with chemotherapy as neoadjuvant therapy in patients with resectable ESCC.Methods: Treatment-naive patients were enrolled and eligible patients received 3 cycles of neoadjuvant therapy with tislelizumab, carboplatin, and nab-paclitaxel. The primary endpoint was surgery patients major pathological response (MPR). Subgroup analysis was stratified by tumor downstaging, circumferential resection margin (CRM), PD-ligand 1 (PD-L1) expression, and tumor mutation burden (TMB). Safety was assessed by adverse events (AEs) and postoperative complications.Results: Between September 2020 and March 2021, 45 patients were enrolled. Thirty-six (80.0%) of 45 patients underwent surgery, and 29 (80.5%) underwent successful R0 resection. MPR and pathological complete response (pCR) for surgery patients were 72.0% and 50.0%, respectively. Intention to treatment (ITT) patients MPR and PCR were 57.5% and 40%. Downgrading occurred in 75% of 36 patients. MPR and pCR were identified to be associated with tumor downstaging and CRM but not PD-L1 expression or TMB. TPS levels in MPR and pCR group were significantly higher than that in Non-MPR and Non-pCR group, respectively. Treatment-related AEs of grade 3-4 and immune-related AEs occurred in 42.2% and 22.2% of 45 patients, respectively, and postoperative complications occurred in 77.8% of 36 patients. No treatment-related surgical delay or death occurred. No associations between gene mutation and pathological efficacy were observed.Conclusions: Tislelizumab plus chemotherapy as neoadjuvant therapy demonstrates promising antitumor activity for resectable ESCC with high rates of MPR, pCR, and R0 resection, as well as acceptable tolerability.
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页数:12
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