Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites

NCT ID: NCT05745233

Last Updated: 2023-08-24

Basic Information

• Recruitment Status: ENROLLING_BY_INVITATION
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-01
• Study Completion Date: 2026-12-31

Brief 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.

Conditions

Malignant Ascites

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Checkpoint inhibitor (nivolumab or pembrolizumab)

Patients with malignant ascites will received either nivolumab or pembrolizumab intraperitoneally.

Group Type: EXPERIMENTAL

Nivolumab

Intervention Type: DRUG

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.

Pembrolizumab

Intervention Type: DRUG

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.

Interventions

Nivolumab

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.

Intervention Type: DRUG

Pembrolizumab

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.

Intervention Type: DRUG

Other Intervention Names

Opdivo; Keytruda

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

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

China Medical University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Li-Yuan Bai

Doctor, Division of Hematology and Oncology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Li-Yuan Bai

Role: PRINCIPAL_INVESTIGATOR

China Medical University Hospital

Locations

China Medical University Hospital

Taichung, Please Select, Taiwan

Countries

Taiwan

References

Wang ST, Chiu CF, Bai HJ, Bai LY. Intraperitoneal nivolumab in a patient with pancreatic cancer and refractory malignant ascites. Eur J Cancer. 2021 May;148:48-50. doi: 10.1016/j.ejca.2021.01.045. Epub 2021 Mar 15. No abstract available.

Reference Type: BACKGROUND

PMID: 33735808 (View on PubMed)

Provided Documents

Document Type: Study Protocol

View Document

Other Identifiers

CMUH107-REC1-180

Identifier Type: -

Identifier Source: org_study_id