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临床试验/NCT02028949
NCT02028949已完成1 期

LIDA-B: Treatment of Cirrhosis-related Hepatocellular Carcinoma With the Intrahepatic Arterial Injection of an Emulsion of Lipiodol and Idarubicin (Zavedos®): Phase I Study

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2012年11月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
15
试验地点
1
主要终点
tolerance: toxicity will be evaluated according to the NCI CTC AE version 4.03 scale to determine the limiting dose

研究概览

简要总结

Unresectable, non-metastatic cirrhosis-related hepatocellular carcinoma (HCC) has a poor prognosis as there are no recommended curative treatments. Chemoembolisation is the most widely used treatment in these patients, but this technique can prove to be toxic. intrahepatic arterial chemotherapy with lipiodol and idarubicin could be an effective therapeutic approach, without deteriorating liver function.

The rationale for this treatment can be resumed as follows:

  • HCC are vascularised via the hepatic artery system
  • The IHA perfusion of anthracyclines leads to high elimination via the liver with low systemic concentrations
  • The absence of embolisation reduces toxicity
  • the toxiciity profile of idarubicin is well known and the drug is widely used for the IV treatment of leukemia
  • idarubicin is the most cytotoxic drug for tumor cell lines.
  • The in vitro cytotoxicity of idarubicin is 100% at low concentrations
  • Lipiodol can stay in contact with tumor tissue for several weeks after injection and act as a vector for the drug
  • The idarubicin-lipiodol is more stable than lipidol emulsions usually given by intraarterial injection
  • The emulsion is more stable with idarubicin than with other anticancer molecules
  • Sequential inclusion in accordance with the "continual reassessment method" makes it possible to increase inclusions at a target toxicity level while reducing inclusions at doses that are too low or too toxic The aim of the treatment is to improve survival.

研究设计

研究类型
Interventional
分配方式
Non Randomized
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically-proven hepatocellular carcinoma or carcinoma meeting validated non-invasive criteria (EASL, AASLD)
  • Child-Pugh A OR B7 cirrhosis
  • General health status WHO 0.1
  • Platelets > 50 000/mm3, Polynuclear neutrophils > 1000/mm3
  • Creatininemia < 1.5 times upper limit of normal
  • LVEF by MUGA scan or US > 50 %
  • Age > 18 years
  • Signed informed consent
  • For women child-bearing age, an effective means of contraception

排除标准

  • Patients who can benefit from curative treatment (surgical resection, liver transplant or treatment via percutaneous destruction)
  • Non-cirrhotic liver
  • Cirrhosis Child B8 or B9 or C
  • Extrahepatic metastases (pulmonary micronodules < 7mm are not considered a contra-indication)
  • Digestive hemorrhage within the previous month
  • Patient on anticoagulants
  • Pregnant women
  • Uncontrolled infection
  • Hypersensitivity to anthracyclines
  • Hypersensitivity to iodine contrast agents
  • Patient under guardianship or ward of court
  • Patients who have already received the recommended cumulative dose of anthracycline (93 mg/m2 for idarubicin, 140 mg/m2 for mitoxantrone, 550 mg/m2 for doxorubicin, 600 mg/m2 for daunorubicin, 900 mg/m2 for epirubicin)

研究组 & 干预措施

Chemo-lipiodol

Experimental

干预措施: Zavedos® (Drug)

Chemo-lipiodol

Experimental

干预措施: Blood samples (Other)

结局指标

主要结局

tolerance: toxicity will be evaluated according to the NCI CTC AE version 4.03 scale to determine the limiting dose

时间窗: 7 weeks after the 2 injections

次要结局

  • Study the pharmacokinetics of idarubicin in this delivery method(24 months)
  • Evaluate overall survival(24 months)
  • Evaluate time to progression(24 months)
  • Evaluate the rate of objective response(24 months)
  • Evaluate progression-free survival(24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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