Circulating tumor DNA as a biomarker in perihilar cholangiocarcinoma: a feasibility study
Completed
- Conditions
- 10019815biliary tract cancerperihilar cholangiocarcinoma
- Registration Number
- NL-OMON43203
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
-Patients older than 18 years
-Undergoing explorative laparotomy, diagnostic laparoscopy or percutaneous biopsy
-Able to understand the information given and provide written informed consent
Exclusion Criteria
-18 years or younger
-Unfit for laparotomy/ diagnostic laparoscopy/ biopsies or blood analyses in palliative
chemotherapy studies
-HIV/AIDS/hepatitis C in medical history
-Not able to give informed consent (language, intellectual capacities, etc.)
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>-To determine if ctDNA is presentcan be reliably detected in patients with PHC.<br /><br>-If ctDNA is presentdetected, we will assess if the mutational profile of the<br /><br>tumor matches the profile of the ctDNA</p><br>
- Secondary Outcome Measures
Name Time Method <p>-To perform a hotspot mutation analysis in patients with pathologically proven<br /><br>PHC</p><br>