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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 16 December 2017
Main ID:  NCT03113604
Date of registration: 10/04/2017
Prospective Registration: No
Primary sponsor: Centre Hospitalier Universitaire, Amiens
Public title: Analysis of the Role of Hepatocyte SLAMF3 Receptor and Drug Resistance Proteins (MDR) in Resistance to Treatment With Sorafenib in CHC Patients SLAMF3
Scientific title: Analysis of the Role of Hepatocyte SLAMF3 Receptor and Drug Resistance Proteins (MDR) in Resistance to Treatment With Sorafenib in CHC Patients
Date of first enrolment: November 20, 2015
Target sample size: 0
Recruitment status: Withdrawn
URL:  https://clinicaltrials.gov/show/NCT03113604
Study type:  Observational
Study design:   
Phase:  N/A
Countries of recruitment
France
Contacts
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients over 18 years of age,

- Diagnosis of hepatocellular carcinoma (histological or non-invasive criteria of
Barcelona),

Group 1: Tumor and peri-tumor tissue samples from patients with untreated CHCs sorafenib

- Patients who received treatment other than sorafenib (chemo-embolization, radiofrequency,
resection, ...),

Group 2: Tumor and peri-tumor tissue samples from patients with non-sorafenib CHC

- Patients treated with sorafenib,

- Patients not responding to treatment with sorafenib

Group 3: Tumor and peri-tumor tissue samples from patients with CHCs responding to
sorafenib

- Patients treated with sorafenib,

- Patients responding to treatment with sorafenib

Exclusion Criteria:

- Age <18 years,

- Patients who do not have liver biopsy specimens (PBH) available at the tumor bank,

- Patients who have refused to use their samples for biomedical research,

- Pregnancy and breast feeding



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Hepatocellular Carcinoma
Hepatocyte Receptor
Intervention(s)
Other: Study on samples of tumor and peri-tumor tissues from patients with hepatocellular carcinoma
Primary Outcome(s)
Rate of expression of SLAM3 and MDR transcripts, correlation with the responder status or not with Sorafenib [Time Frame: 1 day]
Secondary Outcome(s)
Secondary ID(s)
PI2015_843_0021
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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