Actively Recruiting
Role of ctDNA in Genetic Profiling & Outcomes for Advanced BTC
Led by CHA University · Updated on 2026-03-18
200
Participants Needed
1
Research Sites
73 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Biliary tract cancer (BTC) is a rare and heterogeneous disease with high incidence and mortality in Korea. Molecular profiling has enabled the identification of actionable alterations such as Isocitrate Dehydrogenase 1 (IDH1) mutations, FGFR2 fusions, ERBB2 amplifications, and dMMR/MSI-H status. However, the utility of tumor tissue-based next-generation sequencing (NGS) is often limited by difficulties in obtaining adequate tissue samples and the lack of in-house sequencing capacity across many hospitals. Circulating tumor DNA (ctDNA) analysis offers a minimally invasive alternative that can provide rapid and reliable genomic profiling. In a previous study, ctDNA testing showed high concordance with tissue-based genomic profiling for clinically significant alterations, particularly IDH1 mutations, and identified additional mutations not detected in tumor tissue. These findings suggest that ctDNA may expand access to targeted therapies such as ivosidenib . This multicenter, prospective, observational epidemiology study, organized by the Korean Cancer Study Group (KCSG) Biliary Tract Cancer Subcommittee, will evaluate the clinical utility of ctDNA-based genomic profiling in patients with advanced BTC. The study will assess concordance between ctDNA and tumor tissue sequencing, describe the prevalence of actionable alterations, and explore the impact of ctDNA testing on treatment decisions and clinical outcomes. By leveraging a nationwide network of BTC specialists, this study seeks to validate ctDNA as a feasible and scalable tool for precision oncology, supporting timely and personalized therapy for patients with BTC.
CONDITIONS
Official Title
Role of ctDNA in Genetic Profiling & Outcomes for Advanced BTC
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with histologically confirmed advanced or metastatic biliary tract cancer, including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder cancer
- Patients who are either about to start first-line systemic chemotherapy or previously treated patients who can provide a blood sample immediately before starting subsequent therapy
- Age 19 years or older at enrollment
- Willing to provide a blood sample for ctDNA analysis
You will not qualify if you...
- Patients who refuse to provide blood samples for ctDNA testing
- Patients unable to provide written informed consent
- Patients currently enrolled in a similar study at the same institution to avoid duplicate participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Bundang CHA Medical Center
Seongnam-si, Gyeonggi-do, South Korea, 13496
Actively Recruiting
Research Team
H
Hong Jae Chon, MD. PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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