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NCT Number: NCT04556214

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

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..

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Oslo University Hospital

Oslo, 0451, Norway

Location status: Recruiting

Location contact

Magnus Smedman, MD

CONTACT

[email protected]

23026600 ext. 47

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 underlying liver dysfunction
  • No vascular invasion, extrahepatic disease, or lymph node involvement detected on imaging
  • No signs of extrahepatic metastatic disease according to positron emission computed tomography (PET-CT) scan
  • Patient must be accepted for transplantation before progressive disease on chemotherapy.
  • Twelve months or more time span from the diagnosis of iCCA and date of being listed for 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 and follow up
  • Received at least 6 months of chemotherapy or locoregional therapy

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 with the 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

Treatment and study plan

Liver transplant

Procedure

Liver Transplant

Primary outcomes

  1. Overall Survival (OS)

    Time frame: From screening and until 36 months after inclusion

    OS as assessed by quality of life questionnaire (QLQ-C30) patient reported outcome

Secondary outcomes

  1. Overall Survival from time of relapse

    Time frame: From time of relapse and until 36 months after inclusion

    OS as assessed by QLQ-C30 patient reported outcome

  2. Disease free survival

    Time frame: After liver transplantation and up 10 years after liver transplantation

    CT-scan/MRI scan according to RECISTcriteria

  3. Start of new treatment/Change of strategy

    Time frame: Immediately after liver transplatation to start of new treatment

    Time to start of new treatment

  4. Time to decrease in physical function and global health score

    Time frame: Up to 10 years after liver transplantation

    Quality of life measured by EORTC QLQ-C30),

  5. Liver transplant Complication

    Time frame: Up to 90 days after liver transplantation

    Number of Clavien-Dindo grad 3-5 complications

  6. Number of Participants Developing other Malignancies

    Time frame: Up to 10 years after liver transplantation

    Diagnosis of other malignancies

  7. Survival in relation to biological markers

    Time frame: After Liver Transplant until 10 years after liver transplantation

    CEA, CA 19-9 and Germline DNA analyses

Study contacts

Contact information is provided by the study sponsor or research team.

Magnus Smedman, MD

CONTACT

[email protected]

23026600 ext. +47

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Registry information

Important dates

Study start
2020
Primary completion
2035
Study completion
2035
First posted
Sep 21, 2020
Registry last updated
Apr 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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