Induction chemotherapy plus camrelizumab followed by concurrent chemoradiotherapy in unresectable locally advanced esophageal squamous cell carcinoma: a single-arm phase II trial

医学 化学免疫疗法 内科学 肿瘤科 诱导化疗 不利影响 人口 临床研究阶段 放化疗 生活质量(医疗保健) 化疗 置信区间 存活率 临床终点 随机对照试验 危险系数 新辅助治疗 外科 食管癌 临床试验 实体瘤疗效评价标准 无进展生存期 随机化
作者
Fang Peng,Jialiang Wu,Huimin Lian,Shih-Yu Wu,Shaoqing Niu,Xiangbin Xing,Weixiong Yang,Song Wu,Yin Li,Honglan Yu,Shi‐Ting Feng,Xiaoyan Wang,Wenfang Chen,Wen Ye,Tiantian Yu,W.J. Liufu,Chao Cheng,Yong Bao
出处
期刊:Nature Communications [Nature Portfolio]
卷期号:16 (1): 10292-10292
标识
DOI:10.1038/s41467-025-65206-z
摘要

Concurrent chemoradiotherapy (CCRT) has remained the standard treatment for unresectable locally advanced esophageal squamous cell carcinoma (ESCC), yet survival remains poor. This single-arm, phase II trial aims to evaluate the efficacy and safety of two cycles of induction chemotherapy with camrelizumab followed by CCRT in previously untreated patients with unresectable locally advanced ESCC. The primary endpoint, the 1-year overall survival (OS) rate in the per-protocol population (N = 46), was 87.0% (95% confidence interval [CI]: 77.7%-97.3%), exceeding the pre-specified target. Secondary endpoints included OS in the intention-to-treat (ITT) population, progression-free survival (PFS), overall response rate (ORR), disease control rate (DCR), duration of response, safety, and health-related quality of life. In the ITT population (N = 49), the 1-year OS rate was 85.7% (95% CI: 76.5%-96.1%). The 1-year PFS rates in the per-protocol and ITT populations were 71.7% (95% CI: 59.8%-86.0%) and 71.4% (95% CI: 59.8%-85.3%), respectively. The median OS, PFS, and duration of response were not reached. Following CCRT, the ORR was 93.5%, with a DCR of 95.7%. Lymphopenia was the most frequent Grade ≥3 adverse event (100%). One patient died from treatment-related myelosuppression. Health-related quality of life generally improved after induction therapy, with significant improvements in global health status, emotional functioning, and some symptom relief, despite a slight decline in physical functioning. Here, we show that induction chemoimmunotherapy followed by CCRT exhibits promising efficacy and manageable safety in patients with unresectable locally advanced ESCC, thus warranting further randomized controlled trials. Trial number: ChiCTR2000034304.
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