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Living Donor Liver Transplant for Unresectable Colorectal Liver Metastases

Liver Transplantation From Living Donors For Treatment Of Non-Resectable Colorectal Carcinoma Liver Metastases: A Registry Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05248581
Enrollment
25
Registered
2022-02-21
Start date
2019-08-16
Completion date
2027-08-01
Last updated
2026-07-20

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

Conditions

Colorectal Cancer Metastatic

Keywords

liver transplantation, living donor, unresectable colorectal liver metastases

Brief summary

The goal of this study is to create a data registry to capture clinical, pathologic, and molecular data/outcomes for patients with metastatic colorectal cancer who undergo live donor liver transplantation.

Detailed description

The goal of this study is to create a data registry to capture clinical, pathologic, and molecular data/outcomes for patients with metastatic colorectal cancer who undergo live donor liver transplantation. Our primary outcome of interest was the OS and recurrence-free survival (RFS) of patients who underwent LDLT at our center.

Interventions

PROCEDURELiver transplantation

living donor liver transplantation

Sponsors

University of Rochester
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

* Age ≥ 18 * Non-amenable to curative hepatic resection as defined by FLR \<30% * Histologically confirmed adenocarcinoma of the colon or rectum * Candidate for LDLT for colorectal liver metastasis per the University of Rochester liver transplant program

Exclusion criteria

* Not a candidate of the LDLT liver transplant protocol for treatment of colorectal liver metastasis. * Unwilling to consent

Design outcomes

Primary

MeasureTime frameDescription
percentage of patients with recurrence free survival5 yearsRFS proportions to be calculated at 1, 3, and 5 years with Kaplan Meier analysis
percentage overall survival5 yearsOS proportions to be calculated at 1, 3, and 5 years with Kaplan Meier analysis

Countries

United States

Contacts

CONTACTRoberto Hernandez-Alejandro, MD
roberto_hernandez@urmc.rochester.edu585-275-5875
CONTACTJennie Errigo
jennie_errigo@urmc.rochester.edu585-275-5875
PRINCIPAL_INVESTIGATORRoberto Hernandez-Alejandro, MD

University of Rochester

STUDY_DIRECTORMatthew Byrne, MD

University of Rochester

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026