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临床试验/NCT04009265
NCT04009265招募中3 期

Multicenter Prospective Randomized Controlled Study of Adjuvant Chemotherapy, Chemoradiotherapy and Surgery Alone in the Treatment of pN1-2 (pT1b-3N1-2M0) Thoracic Esophageal Squamous Cell Carcinoma

Fujian Medical University Union Hospital1 个研究点 分布在 1 个国家目标入组 819 人开始时间: 2019年8月23日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
819
试验地点
1
主要终点
Overall Survival

研究概览

简要总结

A multi-center prospective randomized controlled study was conducted to compare the effects of adjuvant chemotherapy, chemoradiotherapy and surgery alone for the patients with esophageal cancer.

详细描述

A multi-center prospective randomized controlled study was conducted to compare the effects of adjuvant chemotherapy, chemoradiotherapy and surgery alone on the overall survival rate (OS) and disease-free survival (DFS) of patients with pN1-2 (pT1b-3N1-2M0) thoracic esophageal squamous cell carcinoma, and to observe the safety, side effects of adjuvant therapy and the impact on the quality of life of patients after operation.

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

  • Participants volunteer to participate the study and signed the informed consent.
  • Surgical methods: Radical resection of tumors (R0) was performed, and pathological examination confirmed the diagnosis of thoracic esophageal squamous cell carcinoma.
  • No antineoplastic treatments before operation.
  • According to the 8th edition of AJCC staging, pN1-2 (pT1b-3N1-2M0) stage of esophageal cancer;
  • WHO PS score: 0-1;
  • Age and gender: 18-75 years old, male and female unlimited;
  • Laboratory examination within one week before the adjuvant treatment confirmed that the cardiac, hepatic and renal functions met the requirements.

排除标准

  • The surgical approach is left thoracic approach;
  • Patients with severe postoperative complications who cannot receive adjuvant therapy;
  • Received other anti-tumor treatment before enrollment; At the same time, patients with malignant tumors of other sites were excluded, except non-melanoma skin cancer, in-situ cervical cancer or cured early prostate cancer.
  • Abnormal coagulation function, bleeding tendency (such as active gastrointestinal ulcer) or receiving thrombolytic or anticoagulant treatment;
  • Patients with original severe heart disease, including congestive heart failure, uncontrollable high-risk arrhythmia, unstable angina pectoris, myocardial infarction within half a year, severe heart valve disease and intractable hypertension; Severe hepatic and renal insufficiency;
  • Patients with uncontrollable neurological, mental illness or mental disorder, poor compliance, and inability to cooperate or describe treatment response;
  • Known or suspected allergy to chemotherapeutic drugs.

结局指标

主要结局

Overall Survival

时间窗: 5-year overall survival

overall survival rate of each arms

次要结局

  • Adverse Events(1 year)
  • Scores of Quality of Life(5 years)
  • Disease Free Survival(5-year disease free survival)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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