JPRN-UMIN000004971已完成4 期
Observational study of XELOX in combination with bevacizumab for advanced or recurrent colorectal cancer - KPUMDS C-01 STUDY
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 100
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
- ot applicable 至 ot applicable(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Contraindication of bevacizumab oxaliplatin and capecitabine 2)Brain tumors or brain metastasis 3)Presence of cerebrovascular disease or symptoms less than 1 year prior to entry 4)Any surgical treatments oncluding skin-open biopsy, trauma surgery and other more intensive surgery within 4 weeks or aspiration biopsy within one week 5)Non-healing bone fracture 6)Uncontrolled peptic ulcer 7)Uncontrolled hypertension 8)the internal organ transplant 9)Interstitial pneumonitis, pulmonary fibrosis 10)Uncontrolled Infection 11)Renal failure to be treated, 1+ or higher proteinuria within 1 weeks prior to entry 12)History of adverse events related to DPD loss 13)Daily treatment wit high-dose aspirin (>=325/day) or non-steroidal anti-inflammatory medications 14)Pregnant women, nursing mothers, possibly pregnant women 15)Perforation of gastrointestinal tract less than 1 year prior to entry 16)Clinically significant (i.e. active) cardiovascular disease (>= Grade 2 according to the Common Toxicity Criteria of the National Cancer Institute, version 4), clinically important echocardiographic findigs, or past or current history (within the last 1 year) of myocardial infarction 17)Peripheral neuropathy of at least grade 1 18)Uncontrolled pleural and/or peritoneal effusion 19)Not appropriate for the study at the physician's assessment
研究者
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