Actively Recruiting
Preventive Use of PIPAC in Locally Advanced Gastric Cancer.
Led by National Research Oncology and Transplantology Center, Kazakhstan · Updated on 2025-05-09
160
Participants Needed
1
Research Sites
150 weeks
Total Duration
On this page
Sponsors
N
National Research Oncology and Transplantology Center, Kazakhstan
Lead Sponsor
M
Ministry of Science and Higher Education of the Republic of Kazakhstan
Collaborating Sponsor
AI-Summary
What this Trial Is About
Gastric cancer is the fifth most common cancer worldwide and the third leading cause of cancer-related mortality. In patients with locally advanced gastric cancer, multimodal treatment strategies, including perioperative chemotherapy, have significantly improved survival rates. Despite these advances, peritoneal carcinomatosis (PC) remains a serious problem, occurring in 60% of cases after radical surgery. PC is associated with poor prognosis and limited treatment options. Intra-abdominal chemotherapy, particularly hyperthermic intraperitoneal chemoperfusion (HIPEC), has demonstrated advantages in the treatment of PC. However, a new technique, pressurized intraperitoneal aerosolized chemotherapy (PIPAC), is emerging as a promising alternative. PIPAC delivers chemotherapeutic agents directly to the peritoneal surface as an aerosol, allowing deeper penetration of drugs into tumor implants while minimizing toxicity and invasiveness. This study hypothesizes that the addition of PIPAC as a preoperative treatment for patients with locally advanced gastric cancer may reduce the incidence of peritoneal carcinomatosis compared to standard therapy. The primary objective of this study is to determine whether preoperative PIPAC reduces the incidence of peritoneal carcinomatosis in these patients.
CONDITIONS
Official Title
Preventive Use of PIPAC in Locally Advanced Gastric Cancer.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18-70 years
- Histologically confirmed locally advanced gastric adenocarcinoma (T3-4N0-3M0)
- ECOG performance status 0-2
- Negative peritoneal cytology from diagnostic laparoscopy
- No prior chemotherapy or radiotherapy
- Signed informed consent
You will not qualify if you...
- Presence of distant metastases
- Positive peritoneal cytology
- Previous cancer treatment (chemotherapy, radiotherapy, or surgery)
- Severe comorbid conditions contraindicating surgery or chemotherapy
- Pregnancy or lactation
- Known hypersensitivity to study drugs
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Research Oncology Centre
Astana, Kazakhstan, 010000
Actively Recruiting
Research Team
A
Altay Kerimkulov, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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