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临床试验/NCT03941561
NCT03941561招募中3 期

Compare S-1 for 9 Months to 1 Year as Adjuvant Chemotherapy in Stage II Gastric Cancer (SMAC)

Fudan University6 个研究点 分布在 1 个国家目标入组 1,006 人开始时间: 2019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
3 期
状态
招募中
入组人数
1,006
试验地点
6
主要终点
DFS

研究概览

简要总结

The study aims to compare the efficacy and safety of S-1 for 9 months versus S-1 for 1 year as adjuvant chemotherapy after D2 resection in patients with gastric cancer.

Hypothesis: For gastric patients after D2 resection, S-1 for 9 months shows non-inferiority to S-1 for 1 year in disease-free survival(DFS), overall survival (OS) and safety.

详细描述

It has been identified that S-1 is an effective adjuvant treatment for East Asian patients who have undergone a D2 dissection for locally advanced gastric cancer(GC) in the Japanese Adjuvant Chemotherapy Trial of TS-1(S-1) for Gastric Cancer (ACTS-GC) trail, And S-1 has become one of the standard therapies to these patients. But it is still unknown whether it would improve equally or even more to overall survival(OS) and disease-free survival(DFS) than S-1 for 1 year compared with S-1 for 9 months. As a result, An further clinical trial is still needed, This trial is designed to investigate the efficacy and safety of S-1 for 9 months versus S-1 for 1 year as adjuvant chemotherapy after D2 resection in patients with gastric cancer.

In this study, patients histologically confirmed stage II and who received D2 resection were randomly assigned to receive S-1 for 9 months or S-1 for 1 year. Patients aged from 18 to 75 years and adequate organ function are randomized 1:1 to S-1 for 9 months and S-1 for 1 year. Both are the 3-week recycle of S-1 (80-120mg per day) for 2 weeks, followed by 1 week of rest. The primary endpoint is 3-year DFS, and the secondary endpoint is 5-year OS and safety. Final study analysis will be conducted at the end of the 5th year after the last patient's enrollment. In summary, we hold the hypothesis that S-1 for 9 months is equally effective, safer, and easier to carry out. If possible, there will be a new adjuvant chemotherapy strategy for gastric cancer patients after D2 resection.

To ensure the quality of the study, two interim analyses will be planned at the half and the completion of the study respectively. The DATA and Safety Monitoring Committee will independently review the interim analysis and stop the study ahead of schedule if necessary. Furthermore, to improve the study progress and quality, the in-house interim monitoring will be performed.

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

入选标准

  • The lower age limit of research subjects 18 years old and upper age limit of 75 years old.
  • Be proven to be primary adenocarcinoma of gastric cancer and staged II by pathological evidence
  • R0 surgery with lymphadenectomy
  • Without any other malignancies
  • ECOG (ECOG score standard) performance status of 0 or 1 and expected to survive more than 6 months
  • No contraindications to chemotherapy, including normal peripheral blood routine, liver, and kidney function and electrocardiogram (WBC≥4.0 x 109 /L, NEU≥1.5 x 109 /L, PLT≥100 x 109 /L and HGB≥90g/L).

排除标准

  • Female in pregnancy or lactation, or refuse to receive Contraception measures during chemotherapy.
  • Patients with stage I, III and IV.
  • Unavailable for R0 resection and D2 lymph node dissection.
  • Suffering from other uncontrolled diseases, such as other tumors, acute and Chronic infection.
  • With severe heart disease, including congestive heart failure, uncontrolled arrhythmias, unstable angina, myocardial infarction, severe heart valve disease, and resistant hypertension.
  • Any Known or suspected history of drug allergy test.
  • The researchers believe the patient is not able to complete the entire course of the experiment.
  • Patients (within 4 weeks) are receiving any other anti-cancer drugs therapy, biological therapy, radiation therapy, or Immunosuppressive therapy.
  • Patients conform to any of the following: post-organ transplant, necessary for long-term immunosuppressive or suffering with autoimmune diseases.

研究组 & 干预措施

S-1 for 9 months

Experimental

S-1 80-120mg daily for 14 days in 3 weeks for totally 9 months after D2 resection

干预措施: S-1 for 9 months (Drug)

S-1 for 1 year

Active Comparator

S-1 80-120mg daily for 14 days in 3 weeks for totally 1 year after D2 resection

干预措施: S-1 for 1 year (Drug)

结局指标

主要结局

DFS

时间窗: 3-year

Disease-free survival

次要结局

  • OS(5-year)

研究者

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

Dazhi Xu

Principal Investigator

Fudan University

研究点 (6)

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