Skip to content

HepatoPredict Prognostic Tool for the Decision of Liver Transplant in Hepatocellular Carcinoma

Evaluation of the HepatoPredict Prognostic Tool in the Decision of Liver Transplant in Hepatocellular Carcinoma

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04499833
Acronym
HepatoPredict
Enrollment
40
Registered
2020-08-05
Start date
2021-03-25
Completion date
2029-12-31
Last updated
2022-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma, Scirrhous, Recurrence Tumor

Keywords

cirrhosis, Hepatocellular Carcinoma, liver transplant, tumor recurrence, biomarkers, prognosis

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.

Interventions

PROCEDUREliver transplant

liver transplant

Sponsors

Ophiomics - Precision Medicine
CollaboratorUNKNOWN
Centro Hospitalar de Lisboa Central
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention 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.

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
deathfrom 6 months after liver transplant up to 60 monthsdeath by any cause
hepatocellular carcinoma recurrencefrom 6 months after liver transplant up to 60 monthsidentification of hepatocellular carcinoma recurrence through biannual triphasic CT scan

Secondary

MeasureTime frameDescription
hepatocellular carcinoma recurrence through liquid biopsyfrom 6 months after liver transplant up to 60 monthsearly identification of hepatocellular carcinoma DNA through biannual serum samples (liquid biopsy)

Countries

Portugal

Contacts

Primary ContactHugo Pinto-Marques, MD PhD
hugo.marques3@chlc.min-saude.pt+351917302214
Backup ContactSílvia Gomes-da-Silva, MD
silvia.silva@chlc.min-saude.pt+351916876393

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026