HepatoPredict Prognostic Tool for the Decision of Liver Transplant in Hepatocellular Carcinoma (HepatoPredict)
Primary Purpose
Hepatocellular Carcinoma, Scirrhous, Recurrence Tumor
Status
Recruiting
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
liver transplant
Sponsored by
About this trial
This is an interventional treatment trial for Hepatocellular Carcinoma, Scirrhous focused on measuring cirrhosis, Hepatocellular Carcinoma, liver transplant, tumor recurrence, biomarkers, prognosis
Eligibility Criteria
Inclusion Criteria:
- Hepatocellular carcinoma associated with cirrhosis
- Ages between 18 and 70 years
- Total tumour volume below 500 cm3
- Total number of tumour lesions below 10
- Maximum individual tumour diameter below 10 cm
Exclusion Criteria:
- eligible under the "Milan Criteria"
Sites / Locations
- Centro Hepato-bilio-pancreático e de Transplantação do Hospital Curry CabralRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
liver transplant outside the "Milan Criteria"
Arm Description
patients with hepatocellular carcinoma, outside the "Milan Criteria", that complied with the proposed HepatoPredictTool, submitted to liver transplant
Outcomes
Primary Outcome Measures
death
death by any cause
hepatocellular carcinoma recurrence
identification of hepatocellular carcinoma recurrence through biannual triphasic CT scan
Secondary Outcome Measures
hepatocellular carcinoma recurrence through liquid biopsy
early identification of hepatocellular carcinoma DNA through biannual serum samples (liquid biopsy)
Full Information
NCT ID
NCT04499833
First Posted
July 31, 2020
Last Updated
June 3, 2022
Sponsor
Centro Hospitalar de Lisboa Central
Collaborators
Ophiomics - Precision Medicine
1. Study Identification
Unique Protocol Identification Number
NCT04499833
Brief Title
HepatoPredict Prognostic Tool for the Decision of Liver Transplant in Hepatocellular Carcinoma
Acronym
HepatoPredict
Official Title
Evaluation of the HepatoPredict Prognostic Tool in the Decision of Liver Transplant in Hepatocellular Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 25, 2021 (Actual)
Primary Completion Date
October 30, 2028 (Anticipated)
Study Completion Date
December 31, 2029 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centro Hospitalar de Lisboa Central
Collaborators
Ophiomics - Precision Medicine
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Liver transplant is the most effective treatment for hepatocellular carcinoma (HCC) in cirrhosis. Due to organs shortage, the proper selection of patients is imperative. Prevailing clinical morphological models used in most centres (Milan Criteria), can exclude potential candidates and include patients with aggressive biological behaviour. To more accurately select candidates for liver transplant, the inclusion of criteria that could predict the behaviour and aggressiveness of tumours, such as molecular markers, might be useful.
The investigators propose the use of a new algorithm (HepatoPredict Prognostic Tool), that combine clinical and molecular criteria that address the biology of tumours, in a single centre prospective, intervention study. Data from the "HepatoPredict genomic signature" are added to the clinical and imagiology algorithm. Based on this tool, patients outside the usual eligibility criteria for liver transplant will be proposed for this treatment. These patients will be transplanted with marginal livers or with livers from patients with Familial Amyloid Polyneuropathy, not competing with patients on the waiting list. Patients will be followed up to 60 months after transplant, to assess survival and HCC recurrence with biannual imagiology screening. Survival and disease-free-survival rates will be compared with those obtained by the usual management of patients included and excluded by Milan Criteria.
Detailed Description
Liver transplant is the most effective treatment for hepatocellular carcinoma (HCC) in cirrhosis. Due to organs shortage, the proper selection of patients is imperative. Prevailing clinical morphological models used in most centres (Milan Criteria), can exclude potential candidates and include patients with aggressive biological behaviour. To more accurately select candidates for liver transplant, the inclusion of criteria that could predict the behaviour and aggressiveness of tumours, such as molecular markers, might be useful. The investigators propose the use of a new algorithm (HepatoPredict Prognostic Tool, Ophiomics), combining morphologic information, clinical and molecular criteria, in a prospective, intervention, single centre study.
Patients aged 18 to 70 years, with HCC in cirrhosis, not eligible for liver transplant under the "Milan Criteria", whom had the following morphologic characteristics: total tumour volume below 500 cm3, total number of tumour lesions below 10 and maximum individual tumour diameter below 10 cm, will be proposed for the "HepatoPredict genomic signature" analysis (Ophiomics), obtained from DNA of tumor samples. Those considered candidates by the algorithm are to be proposed for transplant with marginal livers or with livers from patients with Familial Amyloid Polyneuropathy.
Patients will be followed up to 60 months after transplant, to assess survival and HCC recurrence with biannual imagiology screening by triphasic CT scan. Additionally, circulating tumour DNA will be assessed previously to the transplant and biannually for up to 60 months. Survival and disease-free-survival rates will be compared with those obtained with the usual management of patients included and excluded by Milan Criteria, both in the same referral transplant center and in the published literature.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Scirrhous, Recurrence Tumor
Keywords
cirrhosis, Hepatocellular Carcinoma, liver transplant, tumor recurrence, biomarkers, prognosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective evaluation of patients with hepatocellular carcinoma in cirrhotic liver, outside the "Milan Criteria" for liver transplant, that comply with the morphologic criteria stablished for the proposed HepatoPredict Tool: (1) Total tumour volume below 500 cm3; (2) Total number of tumour lesions below 10; and (3) maximum individual tumour diameter below 10 cm. Those patients are proposed to be submitted to molecular study of the hepatocellular carcinoma and, if comply with the "HepatoPredict genomic signature", liver transplantation will be proposed. Patients will be followed up for up to 5 years after transplantation for survival and survival-free-of-disease.
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
liver transplant outside the "Milan Criteria"
Arm Type
Experimental
Arm Description
patients with hepatocellular carcinoma, outside the "Milan Criteria", that complied with the proposed HepatoPredictTool, submitted to liver transplant
Intervention Type
Procedure
Intervention Name(s)
liver transplant
Intervention Description
liver transplant
Primary Outcome Measure Information:
Title
death
Description
death by any cause
Time Frame
from 6 months after liver transplant up to 60 months
Title
hepatocellular carcinoma recurrence
Description
identification of hepatocellular carcinoma recurrence through biannual triphasic CT scan
Time Frame
from 6 months after liver transplant up to 60 months
Secondary Outcome Measure Information:
Title
hepatocellular carcinoma recurrence through liquid biopsy
Description
early identification of hepatocellular carcinoma DNA through biannual serum samples (liquid biopsy)
Time Frame
from 6 months after liver transplant up to 60 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Hepatocellular carcinoma associated with cirrhosis
Ages between 18 and 70 years
Total tumour volume below 500 cm3
Total number of tumour lesions below 10
Maximum individual tumour diameter below 10 cm
Exclusion Criteria:
eligible under the "Milan Criteria"
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hugo Pinto-Marques, MD PhD
Phone
+351917302214
Email
hugo.marques3@chlc.min-saude.pt
First Name & Middle Initial & Last Name or Official Title & Degree
Sílvia Gomes-da-Silva, MD
Phone
+351916876393
Email
silvia.silva@chlc.min-saude.pt
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hugo Pinto-Marques, MD PhD
Organizational Affiliation
Centro Hospitalar Universitário de Lisboa Central
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro Hepato-bilio-pancreático e de Transplantação do Hospital Curry Cabral
City
Lisboa
ZIP/Postal Code
1069-166
Country
Portugal
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hugo Pinto-Marques, MD PhD
Phone
+351917302214
Email
hugo.marques3@chlc.min-saude.pt
First Name & Middle Initial & Last Name & Degree
Luis Pereira-de-Silva, MD PhD
Phone
+351213596402
Ext
51402
Email
centro.investigacao@chlc.min-saude.pt
First Name & Middle Initial & Last Name & Degree
Sílvia Gomes-da-Silva, MD
First Name & Middle Initial & Last Name & Degree
Jose Pereira-Leal, PhD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
HepatoPredict Prognostic Tool for the Decision of Liver Transplant in Hepatocellular Carcinoma
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