Liver Transplant Clinical Trials

Clinical trials related to Liver Transplant Procedure

LIver TrAnspLantation for Non-resectable Peri-HIlar cholangioCArcinoma (LITALHICA)

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

LITALHICA is a prospective non-randomized study aimed at exploring the outcome of liver transplantation in selected patients with unresectable perihilar cholangiocarcinoma (pCCA) after treatment with standard of care chemotherapy, in terms of overall survival and quality of life. Additionally, the study aims to identify pre-transplant biological markers and clinical factors that can stratify patients with the best post-transplant prognosis. Finally, the study aims to investigate the role of preoperative PET-MRI, especially in relation to lymph node locations, by correlating the results with histological examination after hilar lymphadenectomy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Diagnosis of pCCA (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, or biliary ploidy with a malignant appearing stricture on cholangiography)

• Unresectable tumor above cystic duct (pancreatoduodenectomy for microscopic involvement of CBD) or resectable pCCA arising in PSC

• Absence of major vascular invasion, extrahepatic disease, or involvement of regional lymph nodes

• No extrahepatic metastatic disease

• Radial tumor diameter ≤3 cm

• At least six months between first diagnosis of pCCA and date of inclusion

• At least six months of SOC chemotherapy, achieving disease stability or partial response

Locations
Other Locations
Italy
Azienda Ospedale Università di Padova
RECRUITING
Padova
Contact Information
Primary
Enrico Gringeri, Prof.
enrico.gringeri@unipd.it
+39 0498218547
Time Frame
Start Date: 2024-01-15
Estimated Completion Date: 2033-11-01
Participants
Target number of participants: 50
Treatments
Experimental: Study population
Candidates will be evaluated by a National Multidisciplinary Group after routine radiological studies (CT, MRI, PET-MRI/CT).~Patients will receive 6 months of standard of care chemotherapy and undergo PET-MRI with FDG to exclude the presence of extrahepatic disease.~Following completion of therapy, patients will undergo radiological restaging: those who demonstrate stable disease at this stage are considered eligible for definitive listing for LT. Patients will continue chemotherapy until a compatible liver becomes available. If there are no further contraindications, exploratory laparotomy and surgical nodal staging of the tumor will be performed at the time of transplantation. If there are no signs of extrahepatic disease, transplantation will be conducted according to institutional protocols.
Sponsors
Collaborators: Istituto Oncologico Veneto IRCCS
Leads: Azienda Sanitaria Ospedaliera

This content was sourced from clinicaltrials.gov