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临床试验/NCT06341595
NCT06341595招募中2 期

Concurrent Chemoradiotherapy Combined With Sintilimab as Neoadjuvant Therapy for Advanced Gastric Cancer Patients With Para-aortic Lymph Node Metastasis: a Single-arm, Phase II, Exploratory Study.

The First Affiliated Hospital with Nanjing Medical University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
40
试验地点
1
主要终点
Recurrence free survival (RFS)

研究概览

简要总结

This trial is a prospective, single arm, single center, phase II clinical study aimed at subjects with advanced gastric cancer and para aortic lymph node metastasis, exploring the feasibility and safety of Sintilimab Injection combined with synchronous chemo-radiotherapy as neoadjuvant therapy.

Patients will receive sintilimab Injection (200mg iv q3w d1) combined with concurrent radiotherapy and chemotherapy. The chemotherapy regimen will use oxaliplatin 130mg/m2+S-1 40mg/m2 bid d1-14. Radiotherapy is performed using intraperitoneal radiation therapy, once a day, five times a week, at a dose of 1.8-2 Gy/f, for a total of 45-50.4 Gy (60-66 Gy for lymph node lesions). Radiation therapy starts from the second cycle of Sintilimab Injection combined with chemotherapy. The subjects underwent imaging evaluation after completing 4 cycles of combination chemotherapy and radiation therapy with Sintilimab Injection. Evaluated as a surgical subject (surgical conditions: imaging evaluation of enlarged lymph nodes adjacent to the abdominal aorta with PR or no significant activity), radical surgery will be performed within 4 weeks after the last study drug treatment. After surgery, the researcher will determine the necessity of adjuvant treatment and develop an adjuvant treatment plan based on the subject's condition. Subjects evaluated as inoperable will have their best follow-up treatment plan determined by the researcher.

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

combination therapy

Experimental

sintilimab combined with chemotherapy and radiotherapy

干预措施: Sintilimab (Drug)

combination therapy

Experimental

sintilimab combined with chemotherapy and radiotherapy

干预措施: Extraperitoneal radiation therapy (Radiation)

combination therapy

Experimental

sintilimab combined with chemotherapy and radiotherapy

干预措施: Oxaliplatin (Drug)

combination therapy

Experimental

sintilimab combined with chemotherapy and radiotherapy

干预措施: S-1 (Drug)

结局指标

主要结局

Recurrence free survival (RFS)

时间窗: 24 months

Recurrence free survival of patients undergoing surgery after Sintilimab Injection combined with concurrent chemoradiotherapy

次要结局

  • Adverse reactions(24 months)
  • Overall survival (OS)(24 months)
  • R0 resection rate(12 months)
  • Major pathological response rate (MPR)(12 months)
  • Objective response rate (ORR)(24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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