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临床试验/JPRN-UMIN000006307
JPRN-UMIN000006307已完成2 期

Phase II study of S-1 plus irinotecan combined with bevacizumab as 2nd-line chemotherapy in patients with unresectable colorectal cancer, who had previously received oxaliplatin-based chemotherapy. - Phase II study of S-1 plus irinotecan combined with bevacizumab as 2nd-line chemotherapy in patients with unresectable colorectal cancer, who had previously received oxaliplatin-based chemotherapy.(KSCC1102)

Kyushu Study group of Clinical Cancer0 个研究点目标入组 37 人开始时间: 2011年9月8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
37

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

  • 1) Serious complication ( ex. interstitial pneumonitis, pulmonary fibrosis, renal failure, liver failure, poorly-controlled diabetes, poorly-controlled hypertension) 2) Symptomatic or asymptomatic but treated heart disease 3) Active infection.. 4) Pleural effusion, peritoneal fluid 5) History of serious drug hypersensitivity or a history of drug allergy 6) Active other malignancies. 7) History of mental disturbances or cerebrovascular attack, central nervous system disorder 8) Brain metastasis 9) Peptic ulcer, bleeding, intestinal obstruction, intestinal paralysis , gastrointestinal perforation 10) History of gastrointestinal perforation 11) Watery stools or grade 2 or more diarrhea 12) History of thromboembolism, cerebral infarction 13) Hemorrhagic diathesis, coagulation disorder 14) Requiring anti-thrombogenic therapy to prevent thrombosis 15) Requiring steroid drug 16) Receiving flucytosine, atazanavir sulfate 17) Pregnant or lactating woman 18) No birth-control 19) Treatment history of irinotecan 20) History of hemoptysis 21) Contraindication to S-1, CPT-11, bevacizumab 22) High-grade stricture 23) Not appropriate for the study at the physician's assessment

研究者

发起方
Kyushu Study group of Clinical Cancer

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