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NCT Number: NCT06784765

Preventive Use of PIPAC in Locally Advanced Gastric Cancer.

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Research Oncology Centre

Astana, 010000, Kazakhstan

Location status: Recruiting

Location contact

Altay Kerimkulov, MD

CONTACT

[email protected]

+77014382825

About this study

Gastric cancer is the fifth most common cancer globally and the third leading cause of cancer-related death. In patients with locally advanced gastric cancer, multimodal treatment strategies, including perioperative chemotherapy, have significantly improved survival outcomes. However, PC remains a major challenge, often occurring in 60% of cases after radical surgery, and is associated with a poor prognosis and limited treatment options.

Intra-abdominal chemotherapy, particularly HIPEC, has shown benefits in the treatment of PC. However, a newer method, PIPAC, is emerging as a promising alternative. PIPAC delivers chemotherapeutic agents directly to the peritoneal surface via aerosol, ensuring deeper penetration of the drugs into tumor implants and offering lower toxicity and less invasiveness compared to traditional methods.

This study hypothesizes that adding PIPAC as a preoperative treatment in patients with locally advanced gastric cancer may reduce the occurrence of peritoneal carcinomatosis compared to standard therapy alone. PIPAC will be applied before neoadjuvant chemotherapy to patients at high risk for peritoneal recurrence, with the goal of improving survival rates and reducing recurrence after surgery.

The main objectives of this study are to determine whether preoperative PIPAC reduces the incidence of peritoneal carcinomatosis in patients with locally advanced gastric cancer. Secondary objectives include assessing overall survival (OS), progression-free survival (PFS), disease-free survival (DFS), the occurrence of serious adverse events (SAEs), quality of life (QoL) as measured by the EORTC QLQ-C30, postoperative mortality (Clavien-Dindo classification), and pathological response (TRG) in comparison to patients receiving standard treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Adults aged 18-70 years with histologically confirmed locally advanced gastric adenocarcinoma (T3-4N0-3M0), ECOG performance status 0-2, and negative peritoneal cytology.

Inclusion criteria

  • Signed informed consent
  • Aged 18-70 years
  • ECOG performance status 0-2
  • Histologically confirmed adenocarcinoma of the stomach (T3-4N0-3M0)
  • Negative peritoneal cytology from diagnostic laparoscopy
  • No prior chemotherapy or radiotherapy

Exclusion criteria

  • 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

Treatment and study plan

Intervention group

Procedure

Preventive pressurized intraperitoneal aerosol chemotherapy (PIPAC) with cisplatin (10 mg/m2) and doxorubicin (2.1 mg/m2) + perioperative chemotherapy (FLOT regimen) +gastrectomy with D2 lymphadenectomy

Other names: doxorubicin (2.1 mg/m2), cisplatin (10 mg/m2), perioperative chemotherapy (FLOT regimen), gastrectomy, D2 lymphadenectomy, Preventive pressurized intraperitoneal aerosol chemotherapy (PIPAC)

Control Group

Procedure

Retrospective cohort receiving standard perioperative chemotherapy (FLOT regimen) + gastrectomy with D2 lymphadenectomy

Other names: standard perioperative chemotherapy (FLOT regimen), gastrectomy, D2 lymphadenectomy

Primary outcomes

  1. Incidence of peritoneal carcinomatosis

    Time frame: 12, 24 months after surgery

    Incidence of Peritoneal Carcinomatosis refers to the frequency or rate at which new cases of peritoneal carcinomatosis are diagnosed within a specific population over a defined period.

Secondary outcomes

  1. Overall survival

    Time frame: 1. 3, 5 years after surgery

    Overall Survival (OS) refers to the length of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, that patients are still alive.

  2. Disease-free survival

    Time frame: 3, 6, 9, 12, 18, 24 months after surgery

    Disease-Free Survival (DFS) is the period of time after treatment during which a patient shows no signs of the disease.

  3. Quality of life by EORTC QLQ-C30

    Time frame: before surgery, 3 months after surgery, 6 months after surgery, 12 months after surgery

    Quality of life (assessed using European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30), which is calculated in points)

  4. Frequency of adverse events

    Time frame: through study completion, 30 days after surgery, 90 days after surgery

    Frequency of Adverse Events (graded by CTCAE v5.0) refers to the rate or proportion of patients experiencing side effects or complications associated with a treatment, categorized according to severity using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

Study contacts

Contact information is provided by the study sponsor or research team.

Altay Kerimkulov, MD

CONTACT

[email protected]

+77014382825

Sponsors and collaborators

Lead sponsor

National Research Oncology and Transplantology Center, Kazakhstan

Other

Collaborators

  • Ministry of Science and Higher Education of the Republic of Kazakhstan

Registry information

Official study title

Preventive Use of Pressurized Intraperitoneal Aerosol Chemotherapy in Locally Advanced Gastric Cancer: A Non-Randomized Controlled Study

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jan 20, 2025
Registry last updated
May 9, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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