Phase
Condition
Carcinoma
Treatment
Idarubicin and Lipiodol
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Histologically-proven HCC or according to EASL criteria
Child-Pugh A or B7
Disease that is not suitable for resection, ablation or radiofrequency
Performance Status ECOG 0 or 1
BCLC A/B or C if Performance Status ECOG = 1
Measurable lesions according to mRECIST criteria
No previous treatment with chemotherapy, radiotherapy or transarterial embolization (with or without chemotherapy) or radioembolisation
Age superior or equal to 18 years
Platelets > 50,000/mm3, Polynuclear neutrophils > 1000/mm3, Creatininemia < 150umol/L, Bilirubinemia < 5 mg/dL
Absence of heart failure (Ultrasound LVEF > 50%)
Women of child-bearing age using an adequate method of contraception throughouttreatment
Men using an adequate method of contraception throughout the treatment and at least 3 months after the end of treatment
Written informed consent
National health insurance cover
Exclusion
Exclusion Criteria:
Advanced tumor disease (extrahepatic except pulmonary micronodules <7mm of tumoralportal vein thrombosis on positron emission tomography are not a contra-indication.)
Large HCC with liver invasion >50%
History of other cancer than HCC and excluding cancers known to have been cured formore than 5 years, or basocellular skin tumors or cervical cancer in situ treatedwith adequate and curative purpose
Advanced liver disease (Child B8, B9 or C)
Contra-indication for the MRI (Pacemaker or neurosensorial stimulator or implantabledefibrillator, cochlear implant, ferromagnetic foreing body similar to the nervousstructure)
Contra-indication to the injection of the gadolinium-based contrast agents (historyof hypersensibility to the gadolinium chelates, meglumine).
Contra-indication to idarubicin (Hypersensibility to active substance or excipients,cardiopathy with myocardial insufficiency of less than 6 months, seriousarrhythmias, serious renal or liver failure, yellow fever vaccine or any other liveattenuated vaccine, persistente myelosuppression, previous treatments withidarubicin and/or other anthracyclines or anthracenediones at maximum cumulativedoses, stomatitis)
Contra-indication to Lipiodol (Hypersensibility, proven hyperthyroidism, tromaticinjuries, bleeding or recent bleeding)
Concomitant disease or uncontrolled severe clinical situation
Uncontrolled severe infection
Vascular anatomy makes it impossible to perform hepatic intra-arterial treatments
Pregnancy (Beta HCG positive) or breastfeeding
Patient who for psychological, social, family or geographical reasons cannot befollowed regularly
Vulnerable person
Concomitant participation of the patient in another research involving the humanperson
Study Design
Connect with a study center
CHU d'Angers
Angers, 49933
FranceActive - Recruiting
CHU de Dijon
Dijon, 21079
FranceSite Not Available
CHU de Montpellier
Montpellier, 34295
FranceActive - Recruiting
CHU de Nice
Nice, 06202
FranceActive - Recruiting
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