NCT01381211

Brief Summary

Hepatocellular carcinoma (HCC) is a primary malignant tumor of the liver that accounts for an important health problem worldwide. In only 10% - 15% of all patients with HCC, tumors are considered resectable at presentation. In contrast to metastatic liver disease, there is no role for systemic chemotherapy in the treatment of HCC. Today only evidence is available for Sorafenib, a tyrosine kinase inhibiting agent. The arsenal of non-surgical therapies can roughly be divided into local ablative, transarterial and systemic therapies. In well selected patients, local ablative therapy can offer favorable long term results. For patients with disease confined to the liver, but locally more advanced, transarterial treatment modalities are proposed. These therapies exploit the dual blood supply to the liver. HCC derives its blood supply almost entirely from the hepatic artery, while liver parenchyma derives \> 75% of its blood supply from the portal vein. Antitumoral agents, such as cytotoxic drugs or radionuclides, can be delivered in close proximity of the tumor. Examples of transarterial therapies are: transarterial chemoembolization (TACE), bland transarterial embolization (TAE), transarterial chemoembolization with drug eluting beads (TACE-DEB) and transarterial radioembolization with Iodine-131 or Yttrium-90. TACE is currently the gold standard for treatment of patients with intermediate stage HCC, with a reported median survival of around 17 months. A novel development in the TACE treatment for HCC is the drug-eluting bead (DEB). Recently performed small clinical trials reported the efficacy of DEBs in the treatment of intermediate stage HCC, which is substantially higher compared to conventional TACE. Yttrium-90 radioembolization (90Y-RE) is a relatively recently developed technique which implements transarterial administration of minimally embolic microspheres loaded with Yttrium-90, a β-emitting isotope, delivering selective internal radiation to the tumor. In this study the investigators want to prospectively compare TACE-DEB and 90Y-RE, two novel treatments that both have theoretical and/or proven advantages compared to the use of conventional TACE, in patients with intermediate stage HCC.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for phase_2 hepatocellular-carcinoma

Timeline
Completed

Started Sep 2011

Longer than P75 for phase_2 hepatocellular-carcinoma

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 14, 2011

Completed
13 days until next milestone

First Posted

Study publicly available on registry

June 27, 2011

Completed
2 months until next milestone

Study Start

First participant enrolled

September 1, 2011

Completed
6.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2018

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2020

Completed
Last Updated

December 15, 2022

Status Verified

September 1, 2019

Enrollment Period

6.5 years

First QC Date

June 14, 2011

Last Update Submit

December 13, 2022

Conditions

Keywords

Intermediate stage hepatocellular carcinoma

Outcome Measures

Primary Outcomes (1)

  • Time to Progression (TTP).

    Tumor progression is defined according to the modified Response Evaluation Criteria in Solid Tumors (mRECIST) response evaluation criteria. The mRECIST evaluation criteria define progressive disease by the implication of target lesions response, non-target lesions response and the occurrence of new lesions.

    Patients will be followed over a 2 years period.

Secondary Outcomes (6)

  • Time to Local Progression (TLP).

    Since start of treatment untill local tumor progression with a maximum of 2 years follow up.

  • Survival of patients dedicated to either treatment arm.

    Patients are followed for up to 2 years.

  • Quality of life EQ5D

    Before treatment and after treatment on a 3 monthly interval during 2 years.

  • Tumor response to therapy according to mRECIST criteria

    Before treatment and after treatment on a 3 monthly interval during 2 years.

  • Treatment-related costs.

    After follow up of 2 year.

  • +1 more secondary outcomes

Study Arms (2)

Yttrium-90 radioembolization (90Y-RE)

ACTIVE COMPARATOR
Drug: 90Y-RE

Transarterial chemoembolization with drug eluting beads

ACTIVE COMPARATOR

Transarterial chemoembolization is performed with drug eluting beads, polyvinyl alcohol-based microspheres (DC Beads, Biocompatibles) loaded with the chemotherapeutic agent doxorubicin.

Drug: TACE-DEB

Interventions

Transcatheter arterial chemoembolization (TACE) is performed with drug eluting beads (DEB), polyvinyl alcohol-based microspheres loaded with the chemotherapeutic agent doxorubicin.

Transarterial chemoembolization with drug eluting beads
90Y-REDRUG

Glass Yttrium-90 microspheres (TheraSphere®; MDS Nordion Inc.) will be used

Yttrium-90 radioembolization (90Y-RE)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Written informed consent.
  • The diagnosis HCC is confirmed by typical appearance on imaging or cytohistological evaluation (liver biopsy).
  • Accurate staging:
  • MRI of the liver CT-scan of the abdomen and thorax bone scintigraphy, only in case of clinical symptoms suggestive of skeletal metastases.

You may not qualify if:

  • Hypersensitivity to doxorubicin
  • Pregnancy or breastfeeding
  • Age under 18 years
  • Child-Pugh score \>B7
  • ECOG performance status (PST) \> 1
  • Bilirubin \> 2.6 mg/dl
  • AST/ALT \>5x upper limit of normal (ULN)
  • \>50% of liver involvement
  • Main portal vein (right, left or common trunk) thrombosis
  • Extra-hepatic disease
  • Previous treatment of study target lesions
  • mTc-labelled macroaggregated albumin (99mTc-MAA) scintigraphy shows lack of MAA uptake in tumor (photopenic lesion)
  • Activity \> 610 MBq and activity reduction would imply a liver target dose \> 80 Gy
  • patients who are declared incompetent or suffering from physic disorders that make a comprehensive judgement impossible, such as psychosis.
  • Unmanageable intolerance for contrast medium
  • +3 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Ghent

Ghent, 9000, Belgium

Location

Related Publications (2)

  • Dhondt E, Lambert B, Hermie L, Huyck L, Vanlangenhove P, Geerts A, Verhelst X, Aerts M, Vanlander A, Berrevoet F, Troisi RI, Van Vlierberghe H, Defreyne L. 90Y Radioembolization versus Drug-eluting Bead Chemoembolization for Unresectable Hepatocellular Carcinoma: Results from the TRACE Phase II Randomized Controlled Trial. Radiology. 2022 Jun;303(3):699-710. doi: 10.1148/radiol.211806. Epub 2022 Mar 8.

  • Seinstra BA, Defreyne L, Lambert B, Lam MG, Verkooijen HM, van Erpecum KJ, van Hoek B, van Erkel AR, Coenraad MJ, Al Younis I, van Vlierberghe H, van den Bosch MA. Transarterial radioembolization versus chemoembolization for the treatment of hepatocellular carcinoma (TRACE): study protocol for a randomized controlled trial. Trials. 2012 Aug 23;13:144. doi: 10.1186/1745-6215-13-144.

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsLiver NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Study Officials

  • Luc Defreyne, MD, PhD

    University Hospital, Ghent

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 14, 2011

First Posted

June 27, 2011

Study Start

September 1, 2011

Primary Completion

March 1, 2018

Study Completion

March 1, 2020

Last Updated

December 15, 2022

Record last verified: 2019-09

Locations