Overview
This study aims to validate the efficacy and safety of GP/GEMOX combined with PD-1/L1 inhibitors and TKI agents in patients with advanced cholangiocarcinoma through a multicenter, retrospective study to guide clinical practice.
Description
This study plans to enroll patients diagnosed with advanced cholangiocarcinoma. After confirming patients treated with GP/GEMOX or GP/GEMOX combined with PD-1/L1 and TKI agents as initial therapy, the investigators will collect relevant clinical data, including basic clinical information, laboratory data, imaging data, pathological data, and surgical data through an electronic medical record system.
Eligibility
Inclusion Criteria:
- Histologically or radiologically confirmed intrahepatic cholangiocarcinoma
- Initially treated with GP/GEMOX or GP/GEMOX combined with PD-1/L1 and TKI inhibitors
Exclusion Criteria:
- Direct surgery after hospitalization
- Initial treatment combined with local therapies (radiotherapy, radiofrequency, particle implantation, TACE, etc.)
- Initial treatment involving other comprehensive therapeutic regimens