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Prospective Liver Tumor (ProLiT) Database

Prospective Database of Liver Transplantation for Hepatocellular Carcinoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01607788
Acronym
ProLit
Enrollment
500
Registered
2012-05-30
Start date
2009-11-30
Completion date
2017-12-31
Last updated
2012-05-30

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

Conditions

Evidence of Liver Transplantation, Hepatocellular Carcinoma

Keywords

Selection criteria, Liver transplantation, Hepatocellular carcinoma

Brief summary

The investigators propose a prospective, web-based database (developed within the framework of Quickbase, Intuit) which will allow an evaluation of the data for patients with a liver tumour who receive a liver transplant. Each site will continue to transplant according to their own criteria for inclusion on the waiting list. Each center will be responsible to enter a short list of data points at time of listing, transplant, and at 1 and 2 years post transplant. Data will be gathered prospectively through a web-based anaonymized database, and outcomes analyzed yearly X5 for tumour recurrence and patient survival.

Detailed description

A previous retrospective study evaluated the UNOS database of liver transplant recipients for use of total tumor volume (TTV) and alphafetoprotein (AFP) as criteria for selection of candidates for liver transplantation. The results confirmed a prior publication demonstrating that tumors modestly beyond Milan size limitation and irrespective of tumor numbers can achieve excellent outcomes, while providing important insight into which tumors within Milan criteria remain with a high likelihood of recurrence (high AFP). The work has now been published in Hepatology. The investigators propose a prospective evaluation of these composite criteria, using data from patients receiving a liver transplant in order to have a larger population. Centers will continue to transplant according to their own criteria for inclusion on the waiting list. Data will be gathered prospectively through a web-based database (Quickbase, Intuit) and outcomes analyzed yearly for 5 years follow-up for tumour recurrence and patient survival. Each center will be responsible to enter a short list of data points for their patients at time of listing, time of transplant, and yearly post transplant. Data points have been kept to a minimum in the hope that this will encourage participation in this database. The database will be set up with 3 levels of access: 1. data entry only (one at each site) 2. review site data and composite data from other sites(one at each site) 3. review all sites and aggregate (for analysis and publication) Sites will only be able to edit and review their own patient data. They will be able to view aggregate data from other sites from which all identifiers have been removed. Data will not be used to manage patient care in any way. The data will be used only to evaluate outcomes of patients who had a liver tumour at the time of their liver transplant.

Interventions

None listed

Sponsors

University of Alberta
CollaboratorOTHER
London Health Sciences Centre
CollaboratorOTHER
University of Bern
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
University of Geneva, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* patients with hepatocellular carcinoma listed for liver transplantation

Design outcomes

Primary

MeasureTime frame
Post-transplant survival24 months post-transplant

Countries

Canada

Contacts

Primary ContactNorman Kneteman, MD
kneteman@ualberta.ca

Outcome results

None listed

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