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Following People with Colorectal Cancer That Spread to the Liver After Liver Transplant

Follows adults with colorectal cancer spread to the liver who receive a liver transplant.

Plain-language title generated from the registry record
Registry title: Liver Transplantation for Colorectal Cancer

Key facts

Where
Santiago, ChileSee the site

Where in Chile

  • Centro Del Cancer UCSantiago, ChileTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Pontificia Universidad Catolica de Chile
Trial code
NCT07884110
Record updated
20 October 2026
Original description
This is an observational study that will follow adults with stage IV colorectal cancer whose disease has spread only to the liver (not to other organs) and who are undergoing a liver transplant as part of their cancer treatment. Liver transplantation is being offered as a potentially curative option for patients whose liver metastases cannot be surgically removed. Researchers will review participants' medical records for up to 5 years after transplant to understand how this treatment affects survival, cancer recurrence, and safety. Participants will also be asked to complete a quality-of-life questionnaire (EORTC QLQ-C30). Taking part in this study does not involve any additional tests, visits, or procedures beyond the standard care participants would otherwise receive.Read full original descriptionShow less

Liver Transplantation for Colorectal Cancer: a Multicenter Registry

This is an observational study that will follow adults with stage IV colorectal cancer whose disease has spread only to the liver (not to other organs) and who are undergoing a liver transplant as part of their cancer treatment. Liver transplantation is being offered as a potentially curative option for patients whose liver metastases cannot be surgically removed. Researchers will review participants' medical records for up to 5 years after transplant to understand how this treatment affects survival, cancer recurrence, and safety. Participants will also be asked to complete a quality-of-life questionnaire (EORTC QLQ-C30). Taking part in this study does not involve any additional tests, visits, or procedures beyond the standard care participants would otherwise receive.

Inclusion: Adult patients aged 18 years or older at the time of evaluation for liver transplantation; Both male and female patients are eligible; there are no restrictions based on sex or gender; Patients with colorectal cancer (CRC) for whom liver transplantation has been approved as a potential treatment by the institutional liver transplant committee; Histologically confirmed adenocarcinoma of the colon or rectum; Patient not eligible for curative liver resection; Resection of the primary tumor ≥6 months before the planned date of transplantation; Standard surgical procedure with adequate resection margins, including a circumferential resection margin (CRM) of ≥2 mm for patients with rectal cancer; No signs of local recurrence on colonoscopy; Radiological and biomarker (CEA) response to treatment after at least 6 months of systemic therapy. For some higher-risk patients, the multidisciplinary tumor board may require 12 months of response; ECOG performance status 0-1; No signs or history of extrahepatic metastases on chest/abdomen/pelvis computed tomography (CAP CT) or magnetic resonance imaging (MRI), and on whole-body positron emission tomography/computed tomography (PET/CT); Carcinoembryonic antigen (CEA) level below 80 ng/mL at the time of listing for liver transplantation; BRAF wild-type and microsatellite stable (MSS); Deemed an appropriate transplant candidate by the liver transplant candidate evaluation committee and in accordance with transplant selection criteria; A potential living donor available and eligible under Chilean living-donor transplantation law.

Exclusion: Evidence or history of extrahepatic metastases on CT (chest/abdomen/pelvis), MRI, or whole-body PET/CT; BRAF-mutated tumor; Microsatellite instability-high (MSI-H) tumor.

ClinicalTrials.gov NCT07884110