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临床试验/NCT05975749
NCT05975749招募中2 期

A Study of Compared Adjuvant Serplulimab and Trastuzuma and Chemotherapy vs Chemotherapy Only in Her-2 Positive Gastric Cancer With II-III Stage Following Curative Resection

Fudan University1 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2023年1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
114
试验地点
1
主要终点
Disease-free survival

研究概览

简要总结

The purpose of this study is to find out whether treatment with Serplulimab combined with Trastuzumab and Chemotherapy will improve the survival of gastric cancer patients with stage II-III after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Lower age limit of research subjects 20 years old and upper age limit of 80 years old.
  • Be proven to be primary adenocarcinoma of gastric cancer and staged II-III by pathological evidences
  • R0 gastrectomy with D2 lymphadenectomy
  • Her2+ diagnosed by Immunohistochemistry or FISH
  • ECOG (ECOG score standard) performance status of 0 or 1 and expected to survive more than 6 months
  • No contraindications, including normal peripheral blood routine, liver and kidney function and electrocardiogram (WBC≥3.5 x 109 /L, NEU≥1.2 x 109 /L,PLT≥90 x 109 /L and HGB≥80g/L).

排除标准

  • Patients with stage I and IV.
  • Unavailable for R0 resection and D2 lymph node dissection.
  • Multiple primary tumors
  • Suffering from other serious diseases, including cardiovascular, respiratory, kidney, or liver disease, complicated by poorly controlled hypertension, diabetes, mental disorders or diseases.
  • History of chemotherapy, radiotherapy, immunotherapy or target therapy.

研究组 & 干预措施

Adjuvant Treatment of Serplulimab and Trastuzuma and Chemotherapy

Experimental

干预措施: Serplulimab (Drug)

Adjuvant Treatment of Serplulimab and Trastuzuma and Chemotherapy

Experimental

干预措施: Trastuzuma (Drug)

Adjuvant Treatment of Serplulimab and Trastuzuma and Chemotherapy

Experimental

干预措施: Chemotherapy (Drug)

Adjuvant Chemotherapy only

Active Comparator

干预措施: Chemotherapy (Drug)

结局指标

主要结局

Disease-free survival

时间窗: 3-year

DFS

次要结局

  • Side effects(12 months])
  • Overall survival(3-year)

研究者

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

Dazhi Xu

Professor

Fudan University

研究点 (1)

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