Efficacy and Safety of Hepatic Arterial Infusion Chemotherapy Combined With Tislelizumab and Regorafenib as First-Line Therapy for Advanced Cholangiocarcinoma
Efficacy and Safety of Hepatic Arterial Infusion Chemotherapy Combined With Tislelizumab and Regorafenib as First-Line Therapy for Advanced Cholangiocarcinoma: A Single-Centre, Single-Arm, Phase II Trial
The goal of this clinical trial is to evaluate the efficacy and safety of hepatic arterial infusion chemotherapy (HAIC) combined with tislelizumab and regorafenib as first-line therapy in patients with locally advanced or metastatic cholangiocarcinoma.
The main questions it aims to answer are:
- What is the objective response rate (ORR) of this combination regimen according to RECIST 1.1 criteria
- What are the disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and safety profile associated with this treatment
Participants will:Receive hepatic arterial infusion chemotherapy (HAIC)+ tislelizumab (PD-1 inhibitor)+regorafenib (oral multikinase inhibitor). Undergo regular imaging assessments to evaluate tumor response per RECIST 1.1.Be monitored for survival outcomes and adverse events throughout treatment and follow-up.
研究概览
研究类型
注册 (实际的)
阶段
- 阶段2
联系人和位置
学习地点
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Henan
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Zhengzhou、Henan、中国、450052
- The First Affiliated Hospital of Zhengzhou University
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Age 18-75 years ;
- Histologically or cytologically confirmed unresectable locally advanced or metastatic intra- or extrahepatic cholangiocarcinoma ;
- Clinical stage III-IV according to the 8th edition of the AJCC TNM classification ;
- No prior antitumor therapy;
- Child-Pugh liver function class A or B ;
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2;
- At least one measurable lesion per RECIST 1.1 ;
- Adequate haematologic and hepatic/renal function;
- Total bilirubin ≤ 2× upper limit of normal (patients who have undergone biliary drainage are eligible) ;
- Adequate cardiac and pulmonary reserves to tolerate interventional procedures ;
- Signed informed consent, good compliance, and ability to attend follow-up visits.
Exclusion Criteria:
- Contraindications to transarterial chemoembolization, targeted therapy, or immunotherapy ;
- Prior antitumor treatment ;
- Concurrent primary malignancies;
- Child-Pugh class C;
- Severe cardiac, pulmonary, or renal dysfunction ;
- Active autoimmune disease or need for long-term immunosuppressive therapy ;
- Hypersensitivity to contrast agents or study drugs ;
- Pregnancy or lactation;
- Anticoagulant or thrombolytic therapy within 3 months before enrollment or bleeding diathesis.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:HAIC combined with tislelizumab and regorafenib
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A combination therapy including hepatic arterial infusion chemotherapy (HAIC), tislelizumab, and regorafenib for first-line treatment of advanced cholangiocarcinoma.
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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objective response rate (ORR)
大体时间:From first dose until disease progression, death, or up to approximately 24 months
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From first dose until disease progression, death, or up to approximately 24 months
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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disease control rate (DCR)
大体时间:From first dose until disease progression or last tumor assessment, whichever occurs first (up to approximately 24 months)
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From first dose until disease progression or last tumor assessment, whichever occurs first (up to approximately 24 months)
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Progression-Free Survival (PFS)
大体时间:From first dose to disease progression or death from any cause, whichever occurs first (up to approximately 24 months)
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From first dose to disease progression or death from any cause, whichever occurs first (up to approximately 24 months)
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Overall Survival (OS)
大体时间:From first dose to death from any cause (up to approximately 36 months)
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From first dose to death from any cause (up to approximately 36 months)
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adverse events
大体时间:From first dose until 30 days after the last dose of study treatment
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From first dose until 30 days after the last dose of study treatment
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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