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NCT Number: NCT06910722

Liver Transplantation for Locally Advanced Intrahepatic Cholangiocarcinoma After SIRT and Chemotherapy

The study hypothesis is that liver transplantation after selective internal radiation therapy (SIRT) and chemotherapy would improve 3-year overall survival in patients with locally advanced (unresectable but non-metastatic) intrahepatic cholangiocarcinoma.

It is planned to include 36 patients with locally advanced intrahepatic cholangiocarcinoma, not eligible for initial surgery and without metastases. Participants will be recruited from care facilities in France.

Recruiting

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beaujon

Clichy-sous-Bois, France

Location status: Recruiting

Location contact

Mohamed BOUATTOUR

CONTACT

[email protected]

About this study

The hypothesis of the study is that liver transplantation after selective internal radiation therapy (SIRT) and chemotherapy would improve the overall 3-year survival of patients with locally advanced intrahepatic cholangiocarcinoma (unresectable but not metastatic).

All patients over 18 and under 65 years of age with histologically evidence, pauci-nodular (N≤5), locally advanced Intrahepatic cholangiocarcinoma (IHC) without extrahepatic involvement, considered technically unresectable by a panel of experts, eligible for treatment with SIRT, gemcitabine + cisplatin chemotherapy and Liver Transplant (LT).

Following treatment with SIRT + chemotherapy, tumor response or absence of tumor progression will be verified by a morphological workup combining CT-imaging, hepatic MRI and PET-CT.

After exploratory surgery to rule out any contraindications for LT, the patient will be list , with a minimum waiting of 3-month Follow-up will include assesment of Liver graft function, efficiency and tolerance of immunosuppressive therapy.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patient aged 18 to 65
  • With histologically documented intrahepatic cholangiocarcinoma (primary diagnosis):
  • Uni or pauci nodular (≤ 5 lesions (all lesions are counted, even those less than 1 cm))
  • Without extrahepatic or lymph node involvement
  • Technically unresectable R0 according to an expert panel
  • Tumor target > 2 cm
  • WHO 0-1
  • free and informed consent signed
  • highly effective contraception for men and women of childbearing age during study participation up to 2 years post TH

Exclusion criteria

  • Extrahepatic, vesicular or perihilar cholangiocarcinoma
  • Tumor infiltration of more than 50% of the liver
  • Mixed cholangiocarcinoma, hepatocellular carcinoma, fibrolamellar carcinoma
  • Previous treatment for CCI
  • Cirrhosis ≥ Child B7
  • Chronic alcoholism
  • Uncontrolled chronic active infections (patients with HBV, HCV or HDV infections may be included if infections are controlled)
  • Stage III A, IIIB, IV and V chronic renal failure (glomerular filtration rate 59 ml/min)
  • Contraindications to liver transplant
  • Severe untreatable conditions
  • Recent history (less than 5 years) of cancer
  • severe comorbidities
  • Psychiatric or psychological disorders
  • Pregnant or breast-feeding women
  • Patient under guardianship
  • Not affiliated to a Health care system
  • Participating in another interventional study or within the exclusion period of a previous study involving the human body

Treatment and study plan

Liver transplant

Procedure

follow-up of liver transplant patients after selective internal radiotherapy (SIRT) with Yttrium-90 and chemotherapy

Primary outcomes

  1. Strategy efficacy : 3 years overall survival

    Time frame: 3 years post-transplant

    To assess the 3-year overall survival of patients undergoing liver transplantation for stable or downstaged locally advanced intrahepatic cholangiocarcinoma after induction treatment with selective internal radiotherapy and chemotherapy.

Secondary outcomes

  1. Strategy feasibility 1/2

    Time frame: Liver transplantation

    Number of patients benefiting from the complete strategy implemented

  2. Strategy feasibility 2/2 contraindication to transplantation

    Time frame: Liver transplantation

    Number of patients with radiological tumor progression according to RECIST 1.1 criteria after neoadjuvant treatment contraindicating transplantation

  3. Associated factors with the 3-years overall survival

    Time frame: 3 years after strategy implementation

    Socio-demographic and clinico-radio-biological characteristics at baseline and follow-up of living patients 3 years after strategy implementation.

  4. therapeutic efficacy at 3 years

    Time frame: 3 years after strategy implementation

    Number of transplant patients alive and free of recurrence at 3 years after strategy implementation, as well as their socio-demographic and clinico-radiobiological characteristics at baseline and follow-up.

  5. therapeutic efficacy at 5 years

    Time frame: 5 years after strategy implementation

    Number of transplanted patients alive 5 years after the strategy was implemented and number of transplanted patients alive and free of recurrence for the same period;.

  6. oncological prognosis1/2

    Time frame: after 8 courses of chemotherapy

    Number of patients not transplanted alive at 3 years (with or without recurrence)

  7. oncological prognosis 2/2

    Time frame: 5 years after strategy implementation

    Time to onset, type and location of recurrence in transplanted and non-transplanted patients

  8. Histological response

    Time frame: 1 year after strategy implementation

    Rate of tumor necrosis on total hepatectomy specimens in transplant patients

  9. Tolerance of neoadjuvant treatment

    Time frame: after 8 courses of chemotherapy

    Number and type of adverse events induced by neoadjuvant therapy

  10. quality of life monitoring

    Time frame: from induction therapy until 5 years post-transplant

    Changes in scores on the SF-36 quality-of-life questionnaire administered after neoadjuvant treatment prior to TH and then annually between the first and fifth years of follow-up

  11. Tolerance of global strategy

    Time frame: from induction therapy until 3 months post-transplant

    Number of adverse events of grade greater than or equal to 3 (NCI CTCAE) during neoadjuvant treatment + Number of severe complications greater than or equal to 3 of the Clavien-Dindo classification within 90 days of TH.

Study contacts

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

Mohamed BOUATTOUR

CONTACT

[email protected]

1.40.87.56.14 ext. +33

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Liver Transplantation for Locally Advanced Intrahepatic Cholangiocarcinoma After Selective Internal Radiotherapy With Labeled Yttrium and Chemotherapy: a Phase 2 Study

Acronym: RIS-TH

Important dates

Study start
2025
Primary completion
2028
Study completion
2034
First posted
Apr 4, 2025
Registry last updated
Apr 6, 2026

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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