Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites

Trial Title: Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites

NCT ID: NCT05745233

Condition: Malignant Ascites

Conditions: Official terms:
Ascites
Pembrolizumab
Nivolumab

Study type: Interventional

Study phase: N/A

Overall status: Enrolling by invitation

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Nivolumab
Description: Intraperitoneal administration of nivolumab Nivolumab 20 mg in normal saline 100ml will be infused intraperitoneally through a temporary catheter in 10 minutes after paracentesis in a weekly interval.
Arm group label: Checkpoint inhibitor (nivolumab or pembrolizumab)

Other name: Opdivo

Intervention type: Drug
Intervention name: Pembrolizumab
Description: Intraperitoneal administration of pembrolizumab Pembrolizumab 20 mg in normal saline 100ml will be infused intraperitoneally through a temporary catheter in 10 minutes after paracentesis in a weekly interval.
Arm group label: Checkpoint inhibitor (nivolumab or pembrolizumab)

Other name: Keytruda

Summary: This projectis aim to evaluate the efficacy of immune checkpoint inhibitor (pembrolizumab or nivolumab) on the malignant ascites of patients with advanced gastric, pancreatic and biliary tract cancers.

Detailed description: Malignant ascites appear when cancer cells metastasize to peritoneal cavity and interfere the circulation of lymph and blood. Patients with malignant ascites suffer from abdominal fullness, abdominal pain, poor intake, decreased nutrition, disability, and eventually inability to further anticancer treatment. Malignant ascites put a heavy burden on patient, their family, society and health care system. Malignant ascites from cancers of stomach, pancreas and biliary tract are more refractory to intravenous chemotherapy or intraperitoneal chemotherapy than ascites from ovarian or chemo-naïve colorectal cancers because of the inherent nature of chemoresistance. Paracentesis is a treatment with immediate effect but the ascites regrow rapidly and repetitive paracentesis puts patients on the risk of intraabdominal infection. Intraperitoneal infusion of OK-432 can reduce malignant ascites but with intolerable adverse effects of fever, chills, pain, vomiting and septation of ascites which limit the further paracentesis. Cumulating clinical experience suggests a tolerable safety profile of immune checkpoint inhibitors compared to chemotherapy for patients with malignancy. One theoretical advantage of intraperitoneal administration of immune checkpoint inhibitors is the existence of abundant inflammatory cells, immune cells and mesothelial cells dispersed in the malignant ascites. In addition, both pembrolizumab and nivolumab have been administrated intraperitoneally without obvious toxicities in murine tumor models At China Medical University Hospital, one hundred gastric cancer patients, 50 pancreatic cancer patients and 50 biliary tract cancer patients are registered and treated each year. Among them, more than 20 patients suffer from malignant ascites which will ultimately be managed by repeated paracentesis with increasing frequency. Till now, there is no reported or ongoing clinical trial to investigate the efficacy of intraperitoneal checkpoint inhibitor on the malignant ascites.

Criteria for 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

Gender: All

Minimum age: 20 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: China Medical University Hospital

Address:
City: Taichung
Zip: 404
Country: Taiwan

Start date: January 1, 2021

Completion date: December 2026

Lead sponsor:
Agency: China Medical University Hospital
Agency class: Other

Source: China Medical University Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05745233