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.
調査の概要
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
研究場所
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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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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
|
objective response rate (ORR)
時間枠: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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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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disease control rate (DCR)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。