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NCT06140134Recruiting

Liver Transplantation in Intrahepatic Cholangiocarcinoma

A Single-Arm Nonrandomized Phase II Study of Liver Transplantation in Locally Advanced Unresectable Non-Metastatic Intrahepatic Cholangiocarcinoma Treated With Neoadjuvant Systemic Therapy

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

The aim of the current study is to determine the potential efficacy of liver transplantation in the form of patients' overall survival (OS) after neoadjuvant systemic therapy in patients with biologically responsive locally advanced non-metastatic intrahepatic cholangiocarcinoma (iCCA) in comparison to patients historically treated with chemotherapy alone.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
2 Oct 2023
Start date
15 Dec 2023
Primary completion date
Nov 2028
Lead sponsor
Rutgers, The State University of New Jersey
NCT number
NCT06140134

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 15 Dec 2023 to the primary completion date, Nov 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have extrahepatic metastases, lymph node involvement, invasion or encasement of major hepatic vascular structures, perforation of the visceral peritoneum, invasion of extrahepatic structures, invasion of perihilar fat, periductular invasion, concurrent hepatoma or mixed hepatocellular cholangiocarcinoma.
  • Concurrent severe and/or uncontrolled concurrent illness including, but not limited to, ongoing or active infection, acute fulminant liver failure, symptomatic congestive heart failure, unstable angina pectoris, severe uncorrected coronary artery disease, severe cerebrovascular disease, severe pulmonary disease, or psychiatric illness/social situations that would limit compliance with study requirements and that would exclude the patient from eligibility for liver transplantation per institutional protocol.
  • Prior solid organ or bone marrow transplant
  • Previous (within the past 5 years) or concurrent presence of other cancer, except non-melanoma skin cancer and in situ carcinomas.

Other illness

  • Untreated viral hepatitis
  • HIV-infected patients

Age

  • Age \<18 years of age on the day of consenting to the study.

Other

  • Dependent on ≥2 IV inotropic support to maintain hemodynamics
  • Eastern Cooperative Oncology Group (ECOG) Performance Status Scale score \>1 (Karnofsky \<70%, see Appendix A).
  • Unable to understand and sign a written informed consent document
  • Pregnant or breast-feeding women

Who the study is looking for

  • Age ≥18 years of age on the day of consenting to the study.
  • Patients must have histologically confirmed diagnosis of locally advanced intrahepatic cholangiocarcinoma
  • Confirmed diagnosis of locally advanced unresectable iCCA with no vascular invasion, lymph node, or extrahepatic disease.
  • Unresectable disease based on tumor location or underlying liver disease
  • Patients must have ≥ 6 months of disease stability or tumor regression on neoadjuvant therapy. In cases in which patients had received second-line therapy, disease must also have been controlled for ≥ 6 months on that regimen.
  • Patients who had previous surgical resection for iCCA are eligible if surgery occurred more than 6 months prior to listing, and patients have had ≥ 6 months of disease stability or response on therapy.
  • ECOG performance status ≤1 (Karnofsky ≥70%, see Appendix A).
  • Patients must have organ and marrow function acceptable for liver transplantation per institutional protocol:
  • If history of chronic hepatitis B virus (HBV) infection, viral load should be undetectable on suppressive therapy.
  • If history of chronic hepatitis C virus (HCV) infection, patients should have undetectable HCV viral load.
  • Women of child-bearing years must have contraception plan in place from the time of study enrollment until at least one year following liver transplant.
  • Ability to understand and the willingness to sign a written informed consent document
  • Meets all other medical and psychosocial criteria for liver transplant
  • Demonstrate ability to comply with study procedures

Age in the registry: 18 years to 89 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Rutgers New Jersey Medical School
Coordinator of this site? Confirm its status
NewarkUnited StatesRecruiting
University Hospital
Coordinator of this site? Confirm its status
NewarkUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.