JPRN-jRCT1031220613招募中2 期
Biomarker study of FTD/TPI and Bevacizumab as Salvage line chemotherapy for colorectal cancer. - TAS-CC5 Study
Takeshi Yamada0 个研究点目标入组 105 人开始时间: 2023年2月6日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 105
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- >= 20age old 至 <= 80age old(—)
- 性别
- All
入选标准
- •1)Histologically proven colorectal cancer
- •2)patient who has unresectable primary tumor or with one or more unresectable metatatic tumor(s)
- •3)treatment history of two or more regimens for metastatic colorectal cancer, and who has confirmed PD in imaging study
- •4)Patients with unresectable advanced recurrent colorectal cancer who have become refractory or intolerant to fluoropyrimidine anticancer drugs, oxaliplatin, irinotecan, and angiogenesis inhibitors (bevacizumab, ramucirumab, or aflibercept).
- •5)20< and 80> years old
- •6)ECOG performance status of 0 or 1
- •7)With measurable lesions according
- •8)ability to tolerate oral drug administration
- •9)a life expectancy of at least 3 months
- •10)Patient who has adequate main organ functions in tests within 14 days beforeenrollment
- •leukocyte >3,000/mm3
- •neutrophil >1,000/mm3
- •platelet >75,000/mm3
- •haemoglobin concentorarion >8.0 g/dL
- •serum total bilirubin level <1.5 mg/dLserum creatinine <1.5 mg/dL
- •serum AST and ALT levels <5x Upper limit of normal (ULN).
- •serum creatinine <1.5 mg/dL
- •Peripheral neuropathy Diarrhea and NonHaematotoxicity 11)gave written informed consent
排除标准
- •1)contraindications for FTD/TPI and Bevacizumab
- •2)previously received chemotherapy with FTD/TPI
- •3)severe drug allergy
- •4)pregnant woman or Possibility of the pregnant woman. male patient who hoping partner's pregnancy.
- •5)patient who has important clinical complications(symptomatic unstable ischemic heart disease, arrhythmia, acute myocardial infarction within 6 months, liver cirrhosis, renal failure, active gastrointestinal ulcer, ileus, uncontrolled diabetes, uncontrolled hypertension, etc.)
- •6)have pleural effusion and ascitic fluid with the treatment
- •7)Comorbidity or history of heart failure
- •8)gastrointestinal ulcer or bleeding
- •9)previous hemoptysis
- •10)Clinical or radiological evidence of CNS metastases
- •11)Current or previous (within the last 6 months) history of GI perforation
- •12)Patient with interstitial pneumonia or lung fibrosis confirmed in imaging study
- •13)ongoing treatment with anticoagulant
- •14)Synchronous or metachronous multiple malignancy within the last 5 year disease free interval
- •15)Under continuous steroid administration
- •16)decision of unsuitable for this study by the investigator
研究者
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