Liver Transplantation for Non-Resectable Intrahepatic Cholangiocarcinoma: a Prospective Exploratory Trial (TESLA Trial)

Last updated: April 10, 2023
Sponsor: Oslo University Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Biliary Tract Cancer

Abdominal Cancer

Digestive System Neoplasms

Treatment

N/A

Clinical Study ID

NCT04556214
TESLA trial
  • Ages > 18
  • All Genders

Study Summary

The study will investigate whether liver transplantation provides increased survival, low side effects and good quality of life in patients with bile duct cancer where the tumor cannot be removed by normal surgery. Analyzes of blood and tissue samples from the tumor will be investigated to see if the analyzes can indicate who may have recurrence of the disease after liver transplantation. Furthermore, the effect of chemotherapy on normal liver and tumor tissues in the liver that are removed during transplantation will be investigated..

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Histologically verified diagnosis of Intrahepatic Cholangiocarcinoma (iCCA)
  • First time iCCA or liver only recurrence after previous liver resection for iCCA
  • Disease deemed not eligible for liver resection based on tumor location or underlyingliver dysfunction
  • No vascular invasion, extrahepatic disease, or lymph node involvement detected onimaging
  • No signs of extrahepatic metastatic disease according to positron emission computedtomography (PET-CT) scan
  • Patient must be accepted for transplantation before progressive disease onchemotherapy.
  • Twelve months or more time span from the diagnosis of iCCA and date of being listedfor liver transplantation
  • No signs of extrahepatic metastatic disease according to CT or magnetic resonance (MR)scan within 4 weeks prior to the faculty meeting at the transplant unit
  • At least 18 years of age
  • Good performance status, Eastern Cooperative Oncology Group (ECOG) 0 or 1
  • Signed informed consent and expected cooperation of the patients for the treatment andfollow up
  • Received at least 6 months of chemotherapy or locoregional therapy

Exclusion

Exclusion Criteria:

  • Major vascular involvement of the tumor
  • Perforation of the visceral peritoneum
  • Weight loss >15% the last 6 months
  • Patient BMI > 30
  • Other malignancies, except curatively treated more than 5 years ago without relapse
  • Known history of human immunodeficiency virus (HIV) infection
  • Prior history of solid organ or bone marrow transplantation
  • Substance abuse, medical, psychological, or social conditions that may interfere withthe patient's participation in the study or evaluation of the study results
  • Known hypersensitivity to rapamycin
  • Prior extrahepatic metastatic disease
  • Women who are pregnant or breast feeding
  • Any reason why, in the opinion of the investigator, the patient should not participate

Study Design

Total Participants: 15
Study Start date:
June 01, 2020
Estimated Completion Date:
May 31, 2035

Connect with a study center

  • Oslo University Hospital

    Oslo, 0451
    Norway

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.