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.
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Fase 2
Kontakter og lokationer
Studiesteder
-
-
Henan
-
Zhengzhou, Henan, Kina, 450052
- The First Affiliated Hospital of Zhengzhou University
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Eksperimentel: HAIC combined with tislelizumab and regorafenib
|
A combination therapy including hepatic arterial infusion chemotherapy (HAIC), tislelizumab, and regorafenib for first-line treatment of advanced cholangiocarcinoma.
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
objective response rate (ORR)
Tidsramme: From first dose until disease progression, death, or up to approximately 24 months
|
From first dose until disease progression, death, or up to approximately 24 months
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
disease control rate (DCR)
Tidsramme: From first dose until disease progression or last tumor assessment, whichever occurs first (up to approximately 24 months)
|
From first dose until disease progression or last tumor assessment, whichever occurs first (up to approximately 24 months)
|
|
Progression-Free Survival (PFS)
Tidsramme: From first dose to disease progression or death from any cause, whichever occurs first (up to approximately 24 months)
|
From first dose to disease progression or death from any cause, whichever occurs first (up to approximately 24 months)
|
|
Overall Survival (OS)
Tidsramme: From first dose to death from any cause (up to approximately 36 months)
|
From first dose to death from any cause (up to approximately 36 months)
|
|
adverse events
Tidsramme: From first dose until 30 days after the last dose of study treatment
|
From first dose until 30 days after the last dose of study treatment
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Studieafslutning (Faktiske)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- ChiECRCT20220109
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