Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites
Malignant Ascites
About this trial
This is an interventional treatment trial for Malignant Ascites
Eligibility Criteria
Inclusion Criteria: Patients have cyto-/histologically confirmed malignant ascites from gastric, pancreatic or biliary tract adenocarcinoma Patients have malignant ascites more than 1000ml Patients have no history of prior intraperitoneal therapy for malignant ascites Patients have life expectancy of at least 4 weeks Patients have adequate platelet count ≥ 50,000/ul Women or men of reproductive potential should agree to use an effective contraceptive method All patients must be informed of the investigational nature of this study and must sign written informed consents. Exclusion Criteria: Patients have ascites which is related to causes other than the malignancies Patients who are receiving intraperitoneal treatment for their malignant ascites including therapeutic paracentesis Patients with active infection Patients with bleeding disorders Patient with active cardiopulmonary disease or history of ischemic heart disease Patients have intolerant abdominal pain Patients who have serious concomitant systemic disorders incompatible with the study, i.e. poorly controlled diabetes mellitus, auto-immune disorders, cirrhosis of the liver, and the rest will be at the discretion of in-charged investigator
Sites / Locations
- China Medical University Hospital
Arms of the Study
Arm 1
Experimental
Checkpoint inhibitor (nivolumab or pembrolizumab)
Patients with malignant ascites will received either nivolumab or pembrolizumab intraperitoneally.