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NCT Number: NCT06986486

Liver Transplantation for Unresectable Perihilar Cholangiocarcinoma

This is multicentric, single-arm, observational, investigator-drive study investigating the efficacy of liver transplantation after successful downstaging/disease control of unresectable perihilar cholangiocarcinoma using chemotherapy +/- immunotherapy and stereotactic body radiation therapy (SBRT).

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Fondazione IRCCS Istituto Nazionale Tumori di Milano

Milan, Michigan, 20133, Italy

Location status: Recruiting

Location contact

Carlo Sposito, MD

SUB_INVESTIGATOR

Marco Bongini, MD, Ms

SUB_INVESTIGATOR

Marianna Maspero

CONTACT

[email protected]

0223904066 ext. +39

Marianna Maspero, MD

SUB_INVESTIGATOR

Vincenzo Mazzaferro, MD, PhD

PRINCIPAL_INVESTIGATOR

About this study

Patients with unresectable pCCA who fit within inclusion criteria will be enrolled in the study. They will undergo staging laparoscopy with nodal sampling at the hepatic hilum. In case of negative staging (no peritoneal carcinomatosis, no positive hilar lymph nodes, negative peritoneal washing), they will receive downstaging with gemcitabine-cisplatin +/- durvalumab for 2 cycles, followed by SBRT, followed by at least 4 other cycles of gemcitabine-cisplatin +/- durvalumab. After downstaging, they will undergo disease restaging and, if at least disease stability is confirmed, they will undergo transplant screening and listing. Treatment with gemcitabine-cisplatin + durvalumab will continue until liver transplant, progression or unacceptable toxicity.

During listing, restaging will be performed every two months with CT scan and/or MRI, molecular markers and FDG-PET. The target interval between listing and transplant should be less than 90 days.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of unresectable peripheral cholangiocarcinoma arising one centimeter or more above the superior pancreatic margin, with tumor diameter ≤ 3 cm, diagnosed by:
  • Transcatheter biopsy or brush cytology
  • CA-19.9 > 100 mg/ml and/or a mass on cross-sectional imaging with a malignant appearing stricture on cholangiography
  • Biliary ploidy by FISH with a malignant appearing stricture on cholangiography
  • Age between 18 years and 70 years
  • Absence of intra- and extrahepatic metastases
  • Absence of lymph-nodal metastases at any site
  • Biliary stenting of all liver districts
  • No contraindications to liver transplantation
  • No concomitant malignancies or history of other malignancies in the previous 5 years
  • Written informed consent

Exclusion criteria

  • Intrahepatic cholangiocarcinoma
  • Uncontrolled infection
  • Concomitant malignancies or history of other malignancies in the previous 5 years

Treatment and study plan

Primary outcomes

  1. 3-year overall survival

    Time frame: 3 years

    To evaluate overall survival at 36 months in patients with unresectable hilar cholangiocarcinoma treated with neoadjuvant chemotherapy and SBRT followed by liver transplantation according to the modified Mayo Clinic protocol

Secondary outcomes

  1. 3-year recurrence-free survival

    Time frame: 3 years

    To evaluate recurrence-free survival at 36 months in patients with unresectable hilar cholangiocarcinoma treated with neoadjuvant chemotherapy and SBRT followed by liver transplantation according to the modified Mayo Clinic protocol

  2. Safety and feasibility

    Time frame: 3 years

    To evaluate the safety and feasibility of neoadjuvant SBRT and chemotherapy in patients with unresectable hilar cholangiocarcinoma candidate to liver transplantation, in particular we will describe in detail the therapeutic path of all patients with unresectable pCCA that enter within the downstaging pathway and are evaluated for LT, how many are able to be transplanted within this protocol, and what are the reasons for dropout from the protocol

  3. Quality of life

    Time frame: 3 years

    To evaluate the impact of this treatment strategy and of LT on quality of life in patients with unresectable pCCA. Quality of life will be assessed with validated questionnaires. Questionnaires will be performed at baseline and at 6 months intervals; they will be matched and compared with that of eligible patients recruited within the same study period and receiving non-transplant treatments

Study contacts

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

Vincenzo Mazzaferro, MD, PhD

CONTACT

[email protected]

0223902760 ext. +39

Sponsors and collaborators

Lead sponsor

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Other

Registry information

Official study title

Neoadjuvant Chemotherapy and Stereotactic Body Radiation Therapy Followed by Liver Transplantation for Unresectable Perihilar Cholangiocarcinoma: pCOLA

Acronym: pCOLA

Important dates

Study start
2025
Primary completion
2030
Study completion
2030
First posted
May 23, 2025
Registry last updated
May 23, 2025

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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