跳至主要内容
临床试验/JPRN-UMIN000006804
JPRN-UMIN000006804已完成2 期

PhaseII trial of capecitabine plus cisplatin in patients with recurrent HER-2 negative gastric cancer during or after the adjuvant chemotherapy using S-1 (T-CORE1102) - PhaseII trial of capecitabine plus cisplatin for recurrence of HER2 negative cancer patients after S-1 adjuvant chemotherapy (T-CORE1102)

Tohoku Clinical Oncoogy, Research and Education Society(T-CORE)0 个研究点目标入组 21 人开始时间: 2011年12月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
21

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Exclusion criteria were as follows: 1) Cy1. 2) Patients who have been treated with platinum preaviously. 3) A history of drug sensitivity to fluoropyrimidine or platinum 4) Active double cancer within 5 years (except carcinoma in situ and skin cancer which were cured) 5) Active infection or inflammation (fever with 38.0 degree or higher) 6) Active hepatitis 7) Severe heart disease or that history within 1 year. 8) Patient with serious complications such as gastrointestinal paralysis, ileus, interstitial pneumonitis or pulmonary fibrosis, uncontrolled diabetis mellitis, renal failure, liver damage, and liver cirrhosis. 9) Patient who needs treatments of phenytoin or warfarin. 10) Chronic diarrhea (diarrhea of more than 4 times daily, or watery diarrhea) 11) Active GI tract bleeding. 12) Patient who need drainage of peritoneal, pleural or pericardial effusion. 13) Clinically suspicious of brain metastasis, or that history. 14) Pregnancy, possible pregnancy or lactation. 15) Men who wish their partner to become pregnant 16) Treatment or that previous history of psychiatric diseases.

研究者

发起方
Tohoku Clinical Oncoogy, Research and Education Society(T-CORE)

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