Overview

GEMOX Combined With Targeted Therapy and Immunotherapy for Patients With Advanced Cholangiocarcinoma

Status:
Recruiting
Trial end date:
2026-01-15
Target enrollment:
0
Participant gender:
All
Summary
The clinical trial is designed to evaluate the safety and efficacy of GEMOX combined with targeted therapy and immunotherapy for patients with advanced cholangiocarcinoma, and screen the potential biomarkers
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tianjin Medical University Cancer Institute and Hospital
Treatments:
Lenvatinib
Criteria
Inclusion Criteria:

- Male or female, 18 years old ≤ age ≤ 70 years old

- ECOG PS scores 0-1

- Expected survival time > 12 weeks

- Advanced cholangiocarcinoma confirmed by histopathology and/or cytology, locally
advanced (inoperable) or distant metastasis, and with at least one measurable lesion
that has not been locally treated (per RECIST 1.1 criteria)

- Not received any previous systemic or local treatment for the tumor

- Sufficient organ and bone marrow function

Exclusion Criteria:

- Suffered from other malignant tumors in the past 5 years (except Radical basal cell
carcinoma of the skin squamous carcinoma of the skin and/or radical resected carcinoma
in situ)

- Ampullary tumor

- Received treatment from other clinical trials within 4 weeks before the first dose

- Received any anti-PD-1 antibody, anti-PD-L1/L2 antibody, anti-CTLA4 antibody, or other
immunotherapy

- Suffered from severe cardiovascular disease within 12 months before enrollment, such
as symptomatic coronary heart disease, congestive heart failure ≥ Grade II,
uncontrolled arrhythmia, and myocardial infarction

- Uncontrollable pleural effusion, pericardial effusion or ascites

- Use steroids or other systemic immunosuppressive therapies 4 weeks before enrollment

- Allergic reactions to the drugs used in this study

- HIV antibody positive, active hepatitis B or C (HBV, HCV)

- Known history of allogeneic organ transplantation and allogeneic hematopoietic stem
cell transplantation

- other conditions that the investigator deems inappropriate for enrollment