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Cohort of Patients With Hepatocellular Carcinoma or Cholangiocarcinoma

Cohort Study of Patients With Primary Hepatocellular Carcinoma or Cholangiocarcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04340986
Acronym
CHC/CC
Enrollment
1250
Registered
2020-04-10
Start date
2020-09-02
Completion date
2030-09-30
Last updated
2024-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholangiocarcinoma, Hepatocellular Carcinoma

Keywords

hepatocellular carcinoma, cholangiocarcinoma, cohort

Brief summary

The main objective is to describe the evolution of patients treated for a primary malignant hepatobiliary tumor (hepatocellular carcinoma or cholangiocarcinoma) over the long course.

Detailed description

The collection of data from patients with CHC and cholangiocarcinomas who are cancers with poor prognosis is a major challenge to improve patients'care (diagnosis, prognosis); facilitate the search for new therapeutic targets and the follow-up of clinical studies; and develop personalized treatments.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

Inclusion Criteria : * Age ≥ 18 years olds * Medical care in Nephrology department since 2015 Cholangiocarcinoma: \- Histologically and cytologically documented cholangiocarcinoma, regardless of the stage of the disease Hepatocellular carcinoma: * Hepatocellular carcinoma at any stage of the disease, presenting the diagnostic criteria according to the diagnostic criteria of Barcelona : Tumor of more than 1 cm, developed on cirrhosis liver with arterial phase hyperenhancement and washout in the portal venous or delayed phases on CT and MRI * Hepatocellular histologically documented

Exclusion criteria

\- Lack of patient non-opposition

Design outcomes

Primary

MeasureTime frameDescription
Overall survival5 yearsHepatocellular carcinoma and Cholangiocarcinoma : Overall survival is defined as the survival 5 years after the inclusion.

Secondary

MeasureTime frameDescription
Overall survival5 yearsHepatocellular carcinoma :Overall survival is defined as the survival after 5 years of inclusion.
Disease free survival2 and 5 yearsCholangiocarcinoma : 2 and 5 years after surgical resection
Progression time under chemotherapyTime of progression under chemotherapy up to 5 yearsCholangiocarcinoma : Time of progression under chemotherapy is defined by the delay between the start of chemotherapy and tumor progression (appearance of a new lesion or increase in size of more than 30%)

Countries

France

Contacts

Primary ContactMarie LEQUOY, MD
marie.lequoy@aphp.fr+330149283154

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026