ctDNA Detection of MRD in Predicting Postoperative Recurrence in Biliary Tract Cancers：A Multicenter Prospective Trial
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
- Relapse-free survival
研究概览
简要总结
A substantial proporation of patients with biliary tract malignancies still experience disease recurrence after curative resection. ctDNA-based minimal residual disease (MRD) method has been widely used to monitor postoperative recurrence in solid cancers, but few studies have been reported in biliary tract cancers.
The present clinical trial aims to elucidate the correlation between the postoperative ctDNA status and the prognosis of patients with biliary tract cancers, and evaluate whether ctDNA could better predict patients' recurrence and guide clinical practice.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female ≥ 18 years of age on the day of signing informed consent.
- •Clinically diagnosed as BTC before surgery and confirmed by pathology after surgery.
- •Stage I-III tumor according to the UICC/AJCC TNM staging system (8th edition in 2017), meeting the indications for radical surgery and are planned to undergo radical treatment. Those who do not undergo radical surgery will be excluded.
- •Patients must have a performance status of ≤1 on the ECOG Performance Scale.
- •Patients must have survival of > 6 months after surgery
- •Serological tumor indicators (CEA, CA19-9) and imaging data ( CT and/or MRI, PET-CT) were complete.
- •Blood biochemical indicators meet surgical standards
- •Written informed consent must be obtained from patient or patient's legal representative and ability for patient to comply with the requirements of the study.
排除标准
- •Patients with recurrent biliary tract tumors
- •Patients with hepatobiliary mixed tumors
- •Patients with malignant tumors of other organs that have not been cured before.
- •History of organ transplant or allogeneic stem cell transplant
- •Patients with severe infections that are active or poorly controlled clinically
- •patients who are cognitively impaired or with known psychiatric disorders, and/or substance abuse
- •pregnant or lactating women
- •Failed to sign informed consent
- •Other conditions that researchers judged inappropriate for inclusion
结局指标
主要结局
Relapse-free survival
时间窗: through study completion, an average of 2 years
The primary endpoint for this study is Relapse-free survival (RFS), which will be assessed using RECIST version 1.1.
次要结局
未报告次要终点