search
Back to results

Transarterial RAdioembolization Versus ChemoEmbolization for the Treatment of Hepatocellular Carcinoma (HCC) (TRACE)

Primary Purpose

Hepatocellular Carcinoma

Status
Terminated
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
TACE-DEB
90Y-RE
Sponsored by
University Hospital, Ghent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Intermediate stage hepatocellular carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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
  • 99mTc-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
  • Life expectancy < 3 months or otherwise impossible follow-up
  • Inadequate bone marrow, liver and/or renal function
  • other contraindications to hepatic embolization procedures.

Sites / Locations

  • University Hospital Ghent

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Yttrium-90 radioembolization (90Y-RE)

Transarterial chemoembolization with drug eluting beads

Arm Description

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

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Time to Local Progression (TLP).
In both study arms, treatment is done selectively for the lesions within the perfusion area (may be lobar, segmental or subsegmental), as visualized with Cone-Beam CT prior to intervention.
Survival of patients dedicated to either treatment arm.
Survival of patients is followed.
Quality of life EQ5D
Quality of life as measured with The Functional Assessment of Cancer Therapy-Hepatobiliary (FACT-Hep) scale, The Short Form (36) Health Survey, EuroQol Group 5-Dimension Self-Report Questionnaire score (EQ5D) and European Organization for Research and Treatment of Cancer Quality of Life (EORTC-QLQ30).
Tumor response to therapy according to mRECIST criteria
European Association for the Study of the Liver (EASL) response will be obtained based on the following: complete response, partial response, stable disease.
Treatment-related costs.
Treatment-related costs, in terms of cost of therapy and number of hospitalization days, in these patients.
Toxicities and adverse events (recorded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE version 3.0)
The number of patients with AEs, SAEs and SUSARs and the total number of AEs, SAEs and SUSARs in both treatment groups.

Full Information

First Posted
June 14, 2011
Last Updated
December 13, 2022
Sponsor
University Hospital, Ghent
search

1. Study Identification

Unique Protocol Identification Number
NCT01381211
Brief Title
Transarterial RAdioembolization Versus ChemoEmbolization for the Treatment of Hepatocellular Carcinoma (HCC)
Acronym
TRACE
Official Title
Transarterial RAdioembolization Versus ChemoEmbolization for the Treatment of HCC: A Multicenter Randomized Controlled Trial (TRACE Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Terminated
Why Stopped
based on interim analysis results
Study Start Date
September 2011 (Actual)
Primary Completion Date
March 2018 (Actual)
Study Completion Date
March 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Ghent

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
Intermediate stage hepatocellular carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Yttrium-90 radioembolization (90Y-RE)
Arm Type
Active Comparator
Arm Title
Transarterial chemoembolization with drug eluting beads
Arm Type
Active Comparator
Arm Description
Transarterial chemoembolization is performed with drug eluting beads, polyvinyl alcohol-based microspheres (DC Beads, Biocompatibles) loaded with the chemotherapeutic agent doxorubicin.
Intervention Type
Drug
Intervention Name(s)
TACE-DEB
Intervention Description
Transcatheter arterial chemoembolization (TACE) is performed with drug eluting beads (DEB), polyvinyl alcohol-based microspheres loaded with the chemotherapeutic agent doxorubicin.
Intervention Type
Drug
Intervention Name(s)
90Y-RE
Intervention Description
Glass Yttrium-90 microspheres (TheraSphere®; MDS Nordion Inc.) will be used
Primary Outcome Measure Information:
Title
Time to Progression (TTP).
Description
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.
Time Frame
Patients will be followed over a 2 years period.
Secondary Outcome Measure Information:
Title
Time to Local Progression (TLP).
Description
In both study arms, treatment is done selectively for the lesions within the perfusion area (may be lobar, segmental or subsegmental), as visualized with Cone-Beam CT prior to intervention.
Time Frame
Since start of treatment untill local tumor progression with a maximum of 2 years follow up.
Title
Survival of patients dedicated to either treatment arm.
Description
Survival of patients is followed.
Time Frame
Patients are followed for up to 2 years.
Title
Quality of life EQ5D
Description
Quality of life as measured with The Functional Assessment of Cancer Therapy-Hepatobiliary (FACT-Hep) scale, The Short Form (36) Health Survey, EuroQol Group 5-Dimension Self-Report Questionnaire score (EQ5D) and European Organization for Research and Treatment of Cancer Quality of Life (EORTC-QLQ30).
Time Frame
Before treatment and after treatment on a 3 monthly interval during 2 years.
Title
Tumor response to therapy according to mRECIST criteria
Description
European Association for the Study of the Liver (EASL) response will be obtained based on the following: complete response, partial response, stable disease.
Time Frame
Before treatment and after treatment on a 3 monthly interval during 2 years.
Title
Treatment-related costs.
Description
Treatment-related costs, in terms of cost of therapy and number of hospitalization days, in these patients.
Time Frame
After follow up of 2 year.
Title
Toxicities and adverse events (recorded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE version 3.0)
Description
The number of patients with AEs, SAEs and SUSARs and the total number of AEs, SAEs and SUSARs in both treatment groups.
Time Frame
6 months following last treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: 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 99mTc-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 Life expectancy < 3 months or otherwise impossible follow-up Inadequate bone marrow, liver and/or renal function other contraindications to hepatic embolization procedures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luc Defreyne, MD, PhD
Organizational Affiliation
University Hospital, Ghent
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Ghent
City
Ghent
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

Citations:
PubMed Identifier
35258371
Citation
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.
Results Reference
derived
PubMed Identifier
22913492
Citation
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.
Results Reference
derived

Learn more about this trial

Transarterial RAdioembolization Versus ChemoEmbolization for the Treatment of Hepatocellular Carcinoma (HCC)

We'll reach out to this number within 24 hrs