Clinical trial · Interventional
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
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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: 1. What is the objective response rate (ORR) of this combination regimen according to RECIST 1.1 criteria 2. 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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cholangiocarcinoma | Cholangiocarcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| HAIC Combined with Tislelizumab and Regorafenib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- HAIC combined with tislelizumab and regorafenib
- interventionNames
- Drug: HAIC Combined with Tislelizumab and Regorafenib
Primary outcomes (1)
- measure
- objective response rate (ORR)
- timeFrame
- From first dose until disease progression, death, or up to approximately 24 months
Secondary outcomes (4)
- measure
- disease control rate (DCR)
- timeFrame
- From first dose until disease progression or last tumor assessment, whichever occurs first (up to approximately 24 months)
- measure
- Progression-Free Survival (PFS)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age 18-75 years ; 2. Histologically or cytologically confirmed unresectable locally advanced or metastatic intra- or extrahepatic cholangiocarcinoma ; 3. Clinical stage III-IV according to the 8th edition of the AJCC TNM classification ; 4. No prior antitumor therapy; 5. Child-Pugh liver function class A or B ; 6. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2; 7. At least one measurable lesion per RECIST 1.1 ; 8. Adequate haematologic and hepatic/renal function; 9. Total bilirubin ≤ 2× upper limit of normal (patients who have undergone biliary drainage are eligible) ; 10. Adequate cardiac and pulmonary reserves to tolerate interventional procedures ; 11. Signed informed consent, good compliance, and ability to attend follow-up visits. Exclusion Criteria: 1. Contraindications to transarterial chemoembolization, targeted therapy, or immunotherapy ; 2. Prior antitumor treatment ; 3. Concurrent primary malignancies; 4. Child-Pugh class C; 5. Severe cardiac, pulmonary, or renal dysfunction ; 6. Active autoimmune disease or need for long-term immunosuppressive therapy ; 7. Hypersensitivity to contrast agents or study drugs ; 8. Pregnancy or lactation; 9. Anticoagulant or thrombolytic therapy within 3 months before enrollment or bleeding diathesis.
References
Publications (0)
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