KCT0002264招募中未知
Identification of predictive biomarkers for treatment outcome in patients with advanced hepatocellular carcinoma
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 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
- Observational Study
入排标准
- 年龄范围
- 20(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •? unresectable primary liver cancer
- •? Age 20 years old or older
- •? Whole body performance (ECOG) 0-2
- •? Child-Pugh score is B or more
- •? Minimum volume of normal liver without tumor invasion> 1000cm3
- •? Minimum distance between target and organ at risk (eg duodenum, stomach) = 0.5cm
- •? Adequate *LFT (*AST / *ALT <5 x upper limit of normal, total bilirubin> <3 mg / dl, albumin> 2.5 g / dL, normal *PT / *PTT)
- •? Adequate renal function (creatinine <1.8 mg / dl or *Ccr> 50 ml / min)
- •? *BM reserve (*ANC =1500 / mm3, *PLT =50000 / mm3, *Hb> 9 g / dl)
- •? lesion that can be measured or evaluated on CT
- •? Those who are pregnant and who agree to contraception
- •? The person who can read and understand the research agreement and sign the study agreement.
- •*LFT(liver function test)
- •*AST(aspartate aminotransferase)
- •*ALT(alanine Transaminase)
- •*PT(Prothrombin Time)
- •*PTT(Partial Thromboplastin Time)
- •*BM(Bone Marrow)
- •*ANC(Absolute Neutrophil Count)
- •*PLT(Platelet count)
- •*Hb(Hemoglobin)
- •*Ccr(Creatinine clearance)
排除标准
- •? Those who can not perform respiratory training for treatment design
- •? Patients with a history of previous abdominal radiation therapy
- •? Those who can not receive consent before treatment
- •? Those who do not agree to contraception as a pregnant patient
研究者
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