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临床试验/JPRN-jRCT1080221040
JPRN-jRCT1080221040已完成3 期

Randomized phase III study of S-1/Oxaliplatin comparing Tegafur-Uracil/Leucovorin in the Adjuvant chemotherapy of Stage IIIb colorectal cancer.

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 1,200 人开始时间: 2010年3月12日最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
1,200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 80age old(—)
性别
All

入选标准

  • 1) A histopathologically confirmed diagnosis of stage IIIb adenocarcinoma of the colon (from the cecum to the sigmoid [C to S]), rectosigmoid (RS) cancer, or cancer of the rectum above the peritoneal reflection (Ra) (excluding cancer of the appendix).
  • 2) Curability A surgery has been performed.
  • 3) An age of 20 years to 80 years at enrollment.
  • 4) An Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • 5) No treatment other than surgery for the target disease.
  • 6) Oral intake is possible.
  • 7) Adequate major organ function on laboratory testing within 14 days before enrollment. (Testing on the same day of the week 2 weeks before enrollment is permitted.)
  • 8) Treatment can be started within 8 weeks after surgery.
  • 9) Written informed consent has been obtained directly from the patient.

排除标准

  • 1) The inferior tumor margin involves the peritoneal reflection.
  • 2) Active multiple cancer with a disease-free interval of less than 5 years. (Cured basal cell carcinoma or cervical cancer, or gastric cancer, esophageal cancer, or colorectal cancer invading the muscularis propria (pM) that was cured by endoscopic mucosal resection are possible.)
  • 3) Serious postoperative complications (e.g., serious postoperative infections not cured by the time of enrollment, suture failure, and gastrointestinal bleeding).
  • 4) Any of the following concurrent diseases
  • a)Poorly controlled diabetes mellitus
  • b)Poorly controlled hypertension
  • c)Liver cirrhosis or liver failure
  • d)Renal failure
  • e)Interstitial pneumonia, pulmonary fibrosis, or severe emphysema
  • f)Active infectious disease
  • g)Heart failure, myocardial infarction, angina pectoris, or an markedly abnormal electrocardiogram within 6 months before enrollment
  • 5) Neurologic (sensory) disorders
  • 6) Serious diarrhoea
  • 7) A history of serious drug sensitivity
  • 8) Current treatment with flucytosine
  • 9) Women who are pregnant or possibly pregnant, or men who want their partners to bear children
  • 10) Difficulty to participate in clinical studies because of psychological diseases or symptoms
  • 11) Registration in the study is considered inappropriate by the investigator.

研究者

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