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临床试验/NCT06965829
NCT06965829尚未招募2 期

Single-arm Phase II Clinical Study of Neoadjuvant Chemoimmnotherapy Combined With Node Sparing Radiotherapy for Clinical T3N+ Locally Advanced Esophageal Cancer

Shanghai Chest Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年7月1日最近更新:
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Pathological complete remission rate (pCR)

研究概览

简要总结

Background The promising therapeutic outcomes of neoadjuvant chemoimmnotherapy in the treatment of locally advanced esophageal squamous cell carcinoma (ESCC) have been confirmed by several phase II clinical trials and have been widely demonstrated in clinical work. However, in clinical practice, there have been cases of obvious tumor invasion, such as poor tumor regression after cT3 stage receiving NCIT, which reflects the insufficient effectiveness of NCIT for large T type tumors. It may be necessary to add radiotherapy to further improve the local control effect of tumors, but also means higher toxicity reactions. Node sparing radiotherapy can reduce it and enhance the effect of NCIT, which has been applied to the treatment of locally advanced rectal cancer. The aim of this study was to analyze the safety and efficacy of neoadjuvant chemoimmnotherapy combined with node sparing radiotherapy for clinical T3N+ locally advanced esophageal cancer (CINSREC Study).

Methods Forty eligible patients with pathologically confirmed thoracic ESCC of clinical T3N1-3M0 stage were allocated to receive neoadjuvant immunotherapy (tislelizumab 200 mg d1, q3w × 2 cycles) plus chemotherapy (nad-paclitaxel 260 mg/m2 d1 + carboplatin AUC = 5 d1, q3w × 2 cycles) and node sparing radiotherapy (41.4Gy/23 times: 1.8Gy d1-5, qw × 4-5 cycles) treatment. The primary endpoint of this study is pathological complete remission rate (pCR). The secondary endpoints include major pathological response rate, 2-year DFS in pCR patients, adverse events, and overall survival.

Discussion This protocol was reviewed and approved by the Ethics Committee of Shanghai Chest Hospital. This is the first prospective clinical trial to investigate the safety and efficacy of neoadjuvant chemoimmnotherapy combined with node sparing radiotherapy for clinical T3N+ locally advanced esophageal cancer. We hypothesize that this therapy could be a promising therapeutic strategy that can provide better prognosis and safety

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

NCIT combined with node sparing radiotherapy for clinical T3N+ locally advanced esophageal cancer

Experimental

干预措施: Tislelizumab (Drug)

NCIT combined with node sparing radiotherapy for clinical T3N+ locally advanced esophageal cancer

Experimental

干预措施: Carboplatin and Paclitaxel and Radiation Therapy (Drug)

结局指标

主要结局

Pathological complete remission rate (pCR)

时间窗: 12 weeks

次要结局

  • Major Pathological Response Rate (MPR)(12 weeks)
  • Overall survival (OS)(2 years)
  • Disease free survival (DFS)(2 years)
  • Adverse events(12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Guo Xufeng

associate chief physician

Shanghai Chest Hospital

研究点 (1)

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