Cholangiocarcinoma (Bile Duct Cancer) Clinical Trials

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A Prospective, Real-World Study of Alternating Hepatic Arterial Infusion Chemotherapy and Systemic Chemotherapy With or Without Adebrelimab and Apatinib in Patients With Unresectable Biliary Tract Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This prospective real-world study aims to evaluate the effectiveness and safety of an alternating treatment regimen combining hepatic arterial infusion chemotherapy (HAIC) with systemic chemotherapy, with or without adebrelimab and apatinib, in patients with unresectable biliary tract cancer receiving first-line treatment. The study comprises two cohorts: one receiving alternating HAIC and systemic chemotherapy alongside adebrelimab and apatinib, and the other receiving alternating HAIC and systemic chemotherapy alone. Treatment allocation follows real-world clinical decision-making. Patients will be monitored throughout the treatment period to assess tumor response, survival outcomes, and safety profiles. The study aims to generate evidence on the clinical benefits of integrating immunotherapy and targeted therapy into HAIC-based regimens for this patient population.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years at the time of enrollment.

• Histologically or cytologically confirmed diagnosis unresectable, locally advanced, or metastatic BTC, including intrahepatic cholangiocarcinoma, extrahepatic cholangiocarcinoma, and gallbladder cancer.

• No prior systemic therapy for BTC, including chemotherapy, immunotherapy, or small-molecule targeted therapy.

• Patients with disease recurrence ≥6 months after curative resection and completion of adjuvant therapy (chemotherapy or radiotherapy) are eligible.

• Adequate liver function: defined as Child-Pugh Class A (score 5-6) or well-compensated Class B (score ≤7).

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

• At least one measurable lesion as defined by RECIST 1.1.

• Assessed by the investigator as being able to tolerate and comply with the study treatment regimen.

• Provision of written informed consent, voluntarily agreeing to participate after full explanation of the study protocol.

Locations
Other Locations
China
Air Force Military Medical University
RECRUITING
Xi'an
Contact Information
Primary
Jun Tie, Dr
tiejun7776@163.com
+8618629507963
Time Frame
Start Date: 2025-12-10
Estimated Completion Date: 2028-12-30
Participants
Target number of participants: 124
Treatments
Experimental: Alternating HAIC and Systemic Chemotherapy Plus Adebrelimab and Apatinib
Participants in this arm will receive alternating cycles of HAIC and systemic chemotherapy with gemcitabine plus cisplatin, combined with adebrelimab (1200 mg every 3 weeks) and apatinib (250 mg orally once daily). The dosing and administration of HAIC and systemic chemotherapy follow each center's standard treatment protocols.
Active_comparator: Alternating HAIC and Systemic Chemotherapy Alone
Participants in this arm will receive alternating cycles of HAIC and systemic chemotherapy with gemcitabine plus cisplatin. The dosing and administration of HAIC and systemic chemotherapy follow each center's standard treatment protocols.
Related Therapeutic Areas
Sponsors
Leads: Air Force Military Medical University, China

This content was sourced from clinicaltrials.gov