The Application of Pressured Intraperitoneal Aerosol Chemotherapy (PIPAC) for Peritoneal Surface Malignancies

Last updated: April 29, 2026
Sponsor: The University of Hong Kong
Overall Status: Active - Recruiting

Phase

2

Condition

Digestive System Neoplasms

Peritoneal Cancer

Neoplasm Metastasis

Treatment

Pressured Intraperitoneal Aerosol Chemotherapy

Clinical Study ID

NCT06367270
UW 23-361
  • Ages > 18
  • All Genders

Study Summary

Pressurized intraperitoneal aerosol chemotherapy (PIPAC) is a novel minimally invasive drug delivery system for patients with peritoneal metastases (PM). It has been considered as a safe and feasible palliative treatment alternative proven by previous phase I studies. Currently available evidence on feasibility, efficacy and tolerability in Asian populations is limited. In this open-label, single-arm, monocentric clinical trial, investigators aim to evaluate the therapeutic efficacy and complications of PIPAC with oxaliplatin as an alternative on patients of unresectable colorectal cancer with PM and doxorubicin and cisplatin on patients of unresectable gastric and pancreatic cancers with PM. Alternative regimen can be considered multidisciplinary tumour board meeting. Patients will be recruited according to the inclusion criteria and treated for 3 cycles of PIPAC and concurrent systemic chemotherapy. The goal was to repeat PIPAC every 6-8 weeks for at least three procedures, and the delay of the systemic chemotherapy is 2 weeks before and after each PIPAC procedure. If PM was considered to become resectable during PIPAC, patients were discussed at the multidisciplinary tumour board for curative intent cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). The primary outcome is the clinical benefit rate (CBR), measured by an independent radiologist according to Response Evaluation Criteria In Solid Tumors (RECIST) and Peritoneal Cancer Index (PCI) assessed by laparoscopy and histopathological tumour response evaluated by pathologists blinded to clinical outcomes. Key secondary outcomes include the major and minor treatment-related adverse events according to the Common Terminology Criteria for Adverse Events (CTACE) up to 4 weeks after the treatment, Cytological tumour response of peritoneal lavage or ascites, treatment-related characteristics, hospital stay, progression-free survival, overall survival and readmission rate. The proposed study duration is 3 years from the start date and the estimated sample size is 51 according to centre capacity.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. ≥18 years of old;

  2. WHO performance of status 0-1;

  3. Histologically or cytologically proven PM of a gastric, pancreatic or colorectalcarcinoma;

  4. Treatment naïve patients as first-line treatment;

  5. Progression on or intolerance to first-line systemic chemotherapy as second-linetreatment;

  6. No symptoms of gastrointestinal obstruction;

  7. No contraindications for the planned systemic therapy or laparoscopy;

  8. No previous PIPAC/IP/HIPEC;

  9. No other concurrent malignancies or any other malignancy within 6 months prior toenrolment;

  10. Able to give written informed consent.

Exclusion

Exclusion Criteria:

  1. A history of allergic reaction to platinum containing compounds or doxorubicin;

  2. Pregnant or breastfeeding;

  3. Any extra-peritoneal metastases;

  4. Renal impairment, defined as GFR less than 40 mL/min;

  5. Impaired liver function defined as bilirubin over 1.5 × UNL;

  6. Inadequate haematological function

  • Leucocyte < 3.00 × 109/L

  • Absolute neutrophil counts < 1.50 × 109/L

  • Platelet < 100 × 109/L

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: Pressured Intraperitoneal Aerosol Chemotherapy
Phase: 2
Study Start date:
September 01, 2023
Estimated Completion Date:
August 31, 2027

Connect with a study center

  • Queen Mary Hospital

    Hong Kong,
    Hong Kong

    Active - Recruiting

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