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Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites

Primary Purpose

Malignant Ascites

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Nivolumab
Pembrolizumab
Sponsored by
China Medical University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Ascites

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

Checkpoint inhibitor (nivolumab or pembrolizumab)

Arm Description

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

Outcomes

Primary Outcome Measures

Response rate
Control of ascites Rate of ascites control = number of patients who have less ascites determinded by five-point method and subjective symptoms / all patients

Secondary Outcome Measures

Adverse effects
Adverse effect of intraperitoneal immune checkpoint inhibitor Incidence of adverse effect = number of patients who develop a kind of adverse effect / all patients

Full Information

First Posted
February 16, 2023
Last Updated
August 22, 2023
Sponsor
China Medical University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05745233
Brief Title
Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites
Official Title
The Effect of Intraperitoneal Immune Checkpoint Inhibitor on Malignant Ascites of Patients With Gastric, Pancreatic or Biliary Tract Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
China Medical University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Ascites

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Checkpoint inhibitor (nivolumab or pembrolizumab)
Arm Type
Experimental
Arm Description
Patients with malignant ascites will received either nivolumab or pembrolizumab intraperitoneally.
Intervention Type
Drug
Intervention Name(s)
Nivolumab
Other Intervention Name(s)
Opdivo
Intervention 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.
Intervention Type
Drug
Intervention Name(s)
Pembrolizumab
Other Intervention Name(s)
Keytruda
Intervention 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.
Primary Outcome Measure Information:
Title
Response rate
Description
Control of ascites Rate of ascites control = number of patients who have less ascites determinded by five-point method and subjective symptoms / all patients
Time Frame
From the date of registration until the end of treatment, up to 2 years.
Secondary Outcome Measure Information:
Title
Adverse effects
Description
Adverse effect of intraperitoneal immune checkpoint inhibitor Incidence of adverse effect = number of patients who develop a kind of adverse effect / all patients
Time Frame
From the date of registration until treatment termination, up to 2 years.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Li-Yuan Bai
Organizational Affiliation
China Medical University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
China Medical University Hospital
City
Taichung
State/Province
Please Select
ZIP/Postal Code
404
Country
Taiwan

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33735808
Citation
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.
Results Reference
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Intraperitoneal Immune Checkpoint Inhibitor for Malignant Ascites

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