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临床试验/CTIS2023-503341-60-00
CTIS2023-503341-60-00招募中1 期

Efficacy evaluation of 188Re-SSS lipiodol Selective Internal Radiation Therapy of non operable hepatocellular carcinoma patients, a phase II study - 2017-1-14-010

Centre De Lutte Contre Le Cancer Eugene Marquis0 个研究点目标入组 35 人开始时间: 2023年3月21日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
35

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
18 至 65+(—)
性别
All

入选标准

  • •Age = 18 year, ECOG Performance Status 0-1, Hepatocellular Carcinoma with histological diagnosis or non-invasive diagnosis according to AASLD criteria, Non operable and not accessible to ablation therapy, At least one measurable lesion using mRECIST, Tumor involvement <50% of the liver, BCLC classification A to C, Compensated cirrhosis (Child Pugh A or B7), if cirrhosis present, Patient information and signature of informed consent or legal representative

排除标准

  • •Inadequate haematological, hepatic, renal, thyroid and coagulation functions: Haemoglobin < 8,5 g/dl, Granulocytes < 1500/mm3, Platelets< 50 000 /mm3, Bilirubin level = 35 µmol/l, Transaminases > 6 UNL, Creatinine > 1,5 UNL, TSH < 0.2 µUI/L, Contraindication related to the technique, in particular severe arterial pathology of the lower limbs or the aorta contraindicating or making difficult an arteriography by femoral approach, Pregnant woman or likely to be or breastfeeding, or male or female patients of reproductive potential without effective contraception from screening to 1 month after the end of the treatment, Chronic respiratory insufficiency history, Extra-hepatic metastasis except hilum node < 2 cm, Lung shunt >20%, Poor tumor targeting, Previous SIRT, Previous systemic treatment for HCC within 4 weeks before radioembolization, More than 2 previous transcatheter arterial chemoembolization (TACE) (or embolization), in the area to be treated, Other neoplasia except if complete remission from at least one year

研究者

发起方
Centre De Lutte Contre Le Cancer Eugene Marquis

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