Hepatocellular Carcinoma on Cirrhosis With Child A/B7 and Hepatic Intra Arterial Injection of Idarubicin/Lipiodol Emulsion

Last updated: January 20, 2025
Sponsor: University Hospital, Montpellier
Overall Status: Active - Recruiting

Phase

2

Condition

Carcinoma

Treatment

Idarubicin and Lipiodol

Clinical Study ID

NCT03727633
RECHMPL17_0304
UF 9888
2017-004859-22
  • Ages > 18
  • All Genders

Study Summary

The investigators propose in this trial to test a hepatic chemotherapy, consisting of the hepatic intra-arterial injection Idarubicin, emulsified with Lipiodol, lipid vector, without embolization in the treatment of non-metastatic, unresectable hepatocellular carcinoma on cirrhosis with Child-Pugh A/B7.

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

Total Participants: 53
Treatment Group(s): 1
Primary Treatment: Idarubicin and Lipiodol
Phase: 2
Study Start date:
July 19, 2018
Estimated Completion Date:
January 18, 2026

Connect with a study center

  • CHU d'Angers

    Angers, 49933
    France

    Active - Recruiting

  • CHU de Dijon

    Dijon, 21079
    France

    Site Not Available

  • CHU de Montpellier

    Montpellier, 34295
    France

    Active - Recruiting

  • CHU de Nice

    Nice, 06202
    France

    Active - Recruiting

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