RecruitingPhase 3NCT07304271

Intraperitoneal Paclitaxel and Systemic Therapy Versus Systemic Therapy Alone in Gastric Cancer Patients With Peritoneal Metastasis

Randomised Phase III Trial of First Line Intraperitoneal Paclitaxel and Systemic Therapy Versus Systemic Therapy Alone in Gastric Cancer Patients With Peritoneal Metastases - IPa-Gastric


Sponsor

Magnus Nilsson

Enrollment

262 participants

Start Date

Nov 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The most common site for gastric cancer distant metastases is the peritoneum. Median survival for this group of patients is short and systemic cytotoxic treatment response is poor, partly due to the low uptake of the treatment compounds to the peritoneum during systemic chemotherapy. Infusion of cytotoxic drugs directly into the abdominal cavity has been shown to have a high objective response rate and low toxicity. The IPa-Gastric trial is an open-label, multicentre, randomised, phase-III study in the first line setting in gastric cancer patients with peritoneal metastases. Patients will receive the study treatments until disease progression, unacceptable side effects, the investigator's decision to end treatment for other reasons, death, or end of study. After discontinuing study treatments, each patient will be followed up for all study endpoints that are clinically feasible, until death or end of study. The primary objective is to compare overall survival (OS) for patients randomised to intraperitoneal (IP) paclitaxel and standard ST versus those randomised to standard ST only.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding chemotherapy delivered directly into the abdominal cavity (called intraperitoneal paclitaxel) to standard systemic chemotherapy improves outcomes for patients with gastric (stomach) or gastroesophageal junction cancer that has spread to the lining of the abdomen (called peritoneal metastasis). This is a common and difficult-to-treat pattern of spread. **You may be eligible if...** - You have stomach cancer or cancer of the gastroesophageal junction (Siewert type II or III), confirmed by biopsy - Your cancer has spread to the peritoneum (the lining of the abdominal cavity) - You are in good enough overall health to receive chemotherapy - You have not previously received systemic treatment for this cancer **You may NOT be eligible if...** - Your cancer has not spread to the peritoneum - You have already received chemotherapy for this cancer - You have serious organ problems that would make chemotherapy unsafe - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIntraperitoneal Paclitaxel

Intraperitoneally administered Paclitaxel

DRUGStandard systemic therapy

Standard investigator's choice therapy with systemic chemotherapy and any targeted therapies indicated in the standard clinical practice setting


Locations(5)

Azienda Ospedaliera Universitaria Integrata Verona

Verona, Italy

Sahlgrenska University Hospital

Gothenburg, Sweden

Örebro University Hospital

Örebro, Sweden

Karolinska University Hospital

Stockholm, Sweden

Uppsala University Hospital

Uppsala, Sweden

View Full Details on ClinicalTrials.gov

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NCT07304271