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Transarterial Chemoembolization Prior to Transplantation for Hepatocellular Carcinoma

Phase 3
Terminated
Conditions
Hepatocellular Carcinoma
Interventions
Other: Intra-arterial administration of DC BeadsR
Registration Number
NCT01676194
Lead Sponsor
Rennes University Hospital
Brief Summary

The hope to treat more patients with hepatocellular carcinoma successfully is however tempered by the shortage of donors leading to an increasing waiting time for liver transplantation (LT). Intention-to-treat analysis have showed that the reported excellent long-term outcome is curtailed and significantly hampered by the growing incidence of patients who must be removed from the waiting list because of tumor progression. A way to face with this issue is to treat hepatocellular carcinoma prior to LT. Among therapeutic options to impede tumor progression, Transarterial Chemoembolization (TACE) is the most common modality used. While there are many studies concerning TACE in this setting, none are controlled studies and thus there is no firm evidence concerning its efficacy in reducing drop-out or increasing survival. Moreover TACE may induce risks (liver failure, arterial complications...) while waiting for LT. Most of the available data have been based upon analysis of patients who received a transplant and have not included patients who were eligible for LT but died, or showed progression, before it could be performed. Therefore, studies conducted on an intention-to-treat basis are needed to clarify the benefit and the risks of TACE prior to LT in patients with hepatocellular carcinoma.

Detailed Description

* Multicentre, prospective, randomized, 2 parallel group study

* Preoperative evaluation of hepatocellular carcinoma in recipients: Tumor diagnosis will be mainly based upon EASL guidelines. HCCs will be classified according to UCSF criteria (size, number of nodules). Clinical and biological status will be updated every 3 month.

* Pre-transplant treatment:

TACE group: An emulsion of Lipiodol and a cytotoxic drug (50mg/m2 of doxorubicin) will be injected as selectively as possible. Then, an embolic agent will be used to assure stop of flow. The first injection will be performed within 10 days following enlisting and repeated every 8 weeks until LT (only if hypervascularized vital tumor tissue is again visible on CT Scan and if liver function remains within Child A stage) or until complete response. Clinical/biological follow-up will be done once a month.

Control group (no treatment until LT): clinical/biological follow-up and CT-scan every 3 month.

This prospective, multicentric, and randomized study may allow investigators to show that TACE with DC-BeadsR can significantly increase intention to treat survival of patients transplanted for HCC. We also expect that this result will be associated with less recurrence of the cancer after transplantation.

Obviously, we expect that the beneficial effect of TACE will be associated with a acceptable rate of complication related to the procedure.

* Pathologic examination: In all patients in whom LT will be performed, the diagnosis of hepatocellular carcinoma will be confirmed by a histological examination of the explanted liver.

* Dropout criteria: Patients with progression but still meeting the transplant criteria will be maintained in their respective group. Patients with progression over the transplant criteria will be excluded from the waiting list and censored.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
7
Inclusion Criteria
  • Adult patients >18 years
  • With well compensated cirrhosis and hepatocellular carcinoma meeting UCSF criteria
  • Without general contraindication to LT
  • Written informed consent.
Exclusion Criteria
  • Patients that already had TACE
  • Or other local treatment for HCC
  • Or neoadjuvant systemic chemotherapy
  • Or planned living donor
  • Or non arterialized lesion(s)
  • Or Contraindication to DC-BeadsR
  • Or allergy to contrast agents
  • Or contraindication to Doxorubicin.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intra-arterial administration of DC BeadsRIntra-arterial administration of DC BeadsRIntra-arterial administration of DC BeadsR, (1 vial of 100-300 碌m) as selectively as possible loaded with doxorubicin (50 mg per procedure) and mixed with an equal volume of contrast medium. The first injection will be performed within 21 days following enlisting and repeated 1-2 times until LT (only if hypervascularized vital tumor tissue is again visible on CT Scan and if liver function remains within Child A stage) or until complete response
Primary Outcome Measures
NameTimeMethod
Survival3 years

Intention to treat survival at 3 years following inscription on the waiting list for liver transplantation in patient with hepatocellular carcinoma

Secondary Outcome Measures
NameTimeMethod
Allograft survival3 years
Time to dropout3 years
TACE-induced complications (local and general)3 years
Doxorubicin-induced complications3 years
Dropout rate3 years

Dropout rate (tumor progression beyond transplanted criteria and all causes mortality)

Post-transplantation survival rate3 years
Recurrence rate3 years
Contrast agent - induced complications3 years
Efficacy of TACE3 years

Efficacy of TACE (morphological response to TACE: captation rate of Lipiodol and morphological response (RECIST guidelines), as well as histological criteria: percentage of necrosis on pathological examination)

Trial Locations

Locations (7)

H么pital Henri Mondor - Assistance Publique-H么pitaux de Paris

馃嚝馃嚪

Cr茅teil, France

H么pital Michalon, CHU de Grenoble

馃嚝馃嚪

Grenoble, France

H么pital Claude Huriez, CHU de Lille

馃嚝馃嚪

Lille, France

H么pital de la Croix Rousse, HCL, Lyon

馃嚝馃嚪

Lyon, France

H么pital Pontchaillou

馃嚝馃嚪

Rennes, France

H么pital Saint-Antoine / APHP

馃嚝馃嚪

Paris, France

H么pital Trousseau, CHU de Tours

馃嚝馃嚪

Tours, France

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