Trial for Hepatocellular Carcinoma Adjuvant Treatment by Lipiocis (Lipiocis)
|ClinicalTrials.gov Identifier: NCT00116454|
Recruitment Status : Completed
First Posted : June 30, 2005
Last Update Posted : September 23, 2013
|Condition or disease||Intervention/treatment||Phase|
|Carcinoma, Hepatocellular Hepatitis, Viral, Human||Drug: 131 I-lipiodol||Phase 3|
The usual therapeutic approaches of early hepatocellular carcinoma (HCC) are partial hepatectomy or percutaneous ethanol injection. However, these therapeutic procedures do not suppress the cirrhotic liver tissue which represents a major risk factor for recurrence and/or occurrence of a second tumor in the liver. Recently, it has been shown that intra-arterial radioactive lipiodol (Lipiocis®) could reduce the recurrence of cancer and increase the survival after resection of HCC developed on cirrhosis B. The aim of the present randomized and multicenter trial is to investigate the effect of iodine-131-labelled lipiodol (131I-lipiodol = Lipiocis®) in preventing recurrence after curative treatment of HCC (hepatocellular carcinoma) in patients with viral or alcoholic hepatitis related cirrhosis by surgical or percutaneous ablation. The period of this study will be 3 years including 1 year for the enrollment and 2 years for the follow-up. Fifty patients will receive one 2200 MBq dose of Lipiocis and 50 patients will not be treated by Lipiocis (control group). The intra-arterial hepatic administration of Lipiocis will occur 11 to 12 weeks after the initial curative treatment.
The inclusion criteria are as follows : 1) men or women, aged between 18 and 75 years old, with cirrhosis or chronic hepatitis associated with C, B, delta infection or alcool intake or both and confirmed by liver biopsy and 2) one or two HCC nodules treated by surgical or percutaneous ablation (ethanol, acetic acid 50% or radiofrequency).
The efficacy of the initial curative treatment will be assessed by the following criteria: alpha-fetoprotein concentration below 25ng/ml, no progression in size of the tumour demonstrated by ultrasonography and no arterial hypervascularization on CT scan imaging.
The patients with the following criteria will be excluded: co-infection with HIV (Human Immunodeficiency Virus)associated with a CD count <200/mm3 and a viral charge >5000 HIV RNA copies/ml, documented iodine intolerance, respiratory disease, decompensated cirrhosis (Child-Pugh score over or equal 8), bilirubin concentration over 51µmol/l, portal or hepatic vein thrombosis, extra-hepatic metastasis, excessive alcohol intake (over 50g per day), blood platelet count below 50,000/mm3, neutrophil count below 1500/mm3, creatininemia over 120µmol/l, other severe concurrent disease, previous treatment for hepatocellular carcinoma and women who can be pregnant or breastfeeding.
The main endpoint will be to determine whether the Lipiocis® treatment reduces the percentage of recurrence from 50% to 20% at 24 months. The secondary end-points will be the overall survival, the survival without recurrence of the primary tumor, the survival without new tumor, the deterioration of hepatocellular function and the side effects of the Lipiocis® treatment.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||73 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Randomized and Multicenter Trial for Hepatocellular Carcinoma Adjuvant Treatment by Lipiocis|
|Study Start Date :||July 2005|
|Primary Completion Date :||August 2013|
|Study Completion Date :||August 2013|
Experimental: lipiocis group
intra-arterial hepatic administration, one 2200 MBQ dose, duration of treatment 1 week
Drug: 131 I-lipiodol
intra-arterial hepatic administration of Lipiocis will occur, 11 to 12 weeks after the initial curative treatment
Other Name: Lipiocis
No Intervention: control group
- to determine if the Lipiocis treatment decreases the % of tumoral recurrence after 24 months, judged on the rise of alpha-fetoprotein and the reappearance of one or more tumours on the hepatic CT scan [ Time Frame: at 24 Months ]
- overall survival [ Time Frame: at 24 months ]
- recurrence-free survival [ Time Frame: at 24 months ]
- treatment toxicity [ Time Frame: at 24 months ]
- Deterioration of the hepatocellular function [ Time Frame: at 24 months ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00116454
|Service d'Hépatologie Hôpital Saint Antoine|
|Paris, France, 75012|
|Principal Investigator:||Olivier Rosmorduc, MD||Hopital Saint Antoine SERVICE D'HEPATOLOGIE|
|Study Director:||Fabrice Carrat, MD||INSERM U 444 FACULTE DE MEDECINE ST ANTOINE|