医学
诱导化疗
内科学
化疗
放化疗
危险系数
肿瘤科
食管鳞状细胞癌
临床终点
阶段(地层学)
不利影响
B组
基底细胞
A组
临床研究阶段
完全响应
入射(几何)
外科
胃肠病学
癌
放射治疗
随机对照试验
总体生存率
作者
Baoqing Chen,Shiliang Liu,Yujia Zhu,Jingjing Zhang,Yong Bao,Fanjun Meng,Li Zhang,Xingyuan Cheng,Wendi Xuzhang,Biqi Chen,Ruixi Wang,Z. Li,Yonghong Hu,M. LIU,Yingxin Lv,Jibin Li,Mihnea P. Dragomir,Ming Chen,Qiaoqiao Li,Hong Yang
摘要
PURPOSE: To evaluate the efficacy and safety of adding tislelizumab to induction chemotherapy and concurrent chemoradiotherapy (CRT), with or without maintenance immunotherapy, in patients with unresectable locally advanced esophageal squamous cell carcinoma (ESCC). METHODS: This multicenter, randomized, open-label, phase II trial was conducted across four academic hospitals in China (ClinicalTrials.gov identifier: NCT05520619). Participants were adults age 18-70 years with newly diagnosed, unresectable, stage II to IVB ESCC. Patients were randomly assigned (1:1) to receive two cycles of paclitaxel/cisplatin induction chemotherapy followed by concurrent CRT in combination with tislelizumab for 16 cycles in group A (two induction, two concurrent, and 12 maintenance) or four cycles in group B (two induction and two concurrent). The primary end point was progression-free survival (PFS) in the intention-to-treat population, compared with historical control. RESULTS: T-cell density, NRF2 pathway mutations, and dynamic changes in circulating tumor DNA were associated with treatment efficacy. CONCLUSION: The addition of tislelizumab to induction chemotherapy and concurrent CRT without maintenance immunotherapy demonstrated superior efficacy and manageable toxicity in locally advanced ESCC.
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