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临床试验/NCT07151118
NCT07151118招募中不适用

Role of Circulating Tumor DNA (ctDNA) in Genetic Profiling and Clinical Outcomes for Advanced Biliary Tract Cancer (BTC) Patients - Prospective, Observational, Epidemiology Study

CHA University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
1
主要终点
Detection of Actionable Genomic Alterations by ctDNA Profiling

研究概览

简要总结

This prospective, multicenter, observational study aims to evaluate the role of circulating tumor DNA (ctDNA) in advanced or metastatic biliary tract cancer (BTC) patients in Korea. Tissue-based genomic profiling is often limited due to the anatomical challenges of tumor biopsy and insufficient DNA quality. ctDNA analysis offers a minimally invasive alternative for identifying actionable genetic alterations, including Fibroblast Growth Factor Receptor 2 (FGFR2) fusions, Isocitrate Dehydrogenase 1 (IDH1) mutations, and Human Epidermal Growth Factor Receptor 2 (HER2) amplifications. The study will recruit 100 patients across 11 institutions and assess the concordance between ctDNA and tissue genomic profiling, as well as the clinical relevance of ctDNA in predicting treatment outcomes and prognosis.

详细描述

Biliary tract cancer (BTC) is a heterogeneous and aggressive malignancy with poor prognosis, especially in advanced or metastatic stages where surgical resection is not feasible. The current standard first-line therapy with gemcitabine and cisplatin provides limited survival benefit, with median overall survival around 11-12 months. Targeted therapies, such as FGFR inhibitors for FGFR2 fusions and IDH1 inhibitors, as well as immune checkpoint inhibitors, have improved outcomes in subsets of patients. However, tumor tissue acquisition remains challenging in BTC, limiting the ability to perform comprehensive genomic profiling.

Circulating tumor DNA (ctDNA) has emerged as a promising biomarker for molecular profiling, treatment monitoring, and prognosis assessment. Prior studies demonstrated acceptable concordance between ctDNA-based and tissue-based next-generation sequencing, particularly for FGFR2 fusions, and highlighted the potential of ctDNA in identifying additional genomic alterations not detected in tissue samples.

This prospective study will enroll 100 Korean patients with advanced or metastatic BTC from 11 hospitals. Approximately two-thirds of patients will provide blood samples prior to first-line systemic therapy, while one-third will provide samples before subsequent therapy. Additional blood draws will be performed at progression in patients harboring FGFR2 fusion, IDH1 mutation, or HER2 amplification. Collected samples will be analyzed by a central laboratory (SCL Healthcare, a precision medicine service provider specializing in biomarker-based diagnostics).

The primary objective is to evaluate the frequency of actionable genomic alterations, especially FGFR2 fusions, detected by ctDNA in advanced BTC patients. Secondary objectives include:

  • Assessing the concordance between ctDNA and tissue genomic profiling
  • Evaluating the proportion of patients who received targeted therapy based on ctDNA results (e.g., pemigatinib [Pemazyre®])
  • Exploring associations between ctDNA maximum variant allele frequency (max VAF) and survival outcomes
  • Identifying potential resistance mechanisms and clonal evolution during targeted therapy

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Histologically confirmed advanced or metastatic biliary tract cancer (including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder carcinoma)
  • •Patients meeting one of the following conditions:
  • •Prior to initiation of first-line systemic therapy
  • •Patients who previously received systemic therapy and are able to provide a blood sample prior to initiation of subsequent therapy
  • •Age ≥ 19 years at the time of enrollment
  • •Willingness and ability to provide blood samples for ctDNA analysis

排除标准

  • •Refusal to provide blood samples for ctDNA testing
  • •Inability to provide written informed consent

研究组 & 干预措施

Advanced Biliary Tract Cancer Patients

Patients with histologically confirmed advanced or metastatic biliary tract cancer (intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, or gallbladder cancer). Participants will provide blood samples for circulating tumor DNA (ctDNA) analysis before systemic therapy or prior to subsequent treatment.

干预措施: Blood Sampling for ctDNA Analysis (Other)

结局指标

主要结局

Detection of Actionable Genomic Alterations by ctDNA Profiling

时间窗: Baseline (within 30 days prior to initiation of systemic therapy or prior to subsequent treatment)

Frequency of targetable genetic alterations, especially FGFR2 fusion, detected in ctDNA from patients with advanced biliary tract cancer.

次要结局

  • Frequency of Specific Genomic Alterations by ctDNA Analysis(Up to 24 months)
  • Proportion of Patients Receiving Targeted Therapy Based on ctDNA Findings(Up to 24 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hong Jae Chon

Principal Investigator

CHA University

研究点 (1)

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