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Quantitation of Intra-peritoneal Ovarian Cancer Metastasis
Published on: July 18, 2016
Intraperitoneal chemotherapy for advanced epithelial ovarian malignancy: lessons learned.
Michael Bunting1, Warren Chan, Alison Brand
1Department of Obstetrics and Gynaecology, The Royal Hobart Hospital, Hobart, Tasmania. michael.bunting@hnehealth.nsw.gov.au
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|January 15, 2010
Summary
Intraperitoneal (IP) chemotherapy offers survival benefits for advanced ovarian cancer but presents challenges. This Australian study found IP chemotherapy feasible, though toxicities and administration issues led to treatment discontinuation in some patients.
Area of Science:
- Gynecologic Oncology
- Medical Oncology
- Clinical Pharmacology
Background:
- Intraperitoneal (IP) chemotherapy improves survival in advanced ovarian cancer compared to intravenous (IV) chemotherapy.
- However, IP chemotherapy is associated with increased adverse events, toxicities, and administration challenges.
- These challenges include technical difficulties and demanding schedules.
Purpose of the Study:
- To report the initial experience with IP chemotherapy administration in Australia.
- To evaluate the feasibility and practicality of IP chemotherapy in two Australian gynaecological oncology units.
Main Methods:
- Retrospective data collection from 23 women with advanced ovarian cancer receiving adjuvant IP chemotherapy.
- Collection of standard toxicity data (CTCAE v3.0) and IP-specific administration data.
Main Results:
- Patients received an average of 4.3 IP chemotherapy cycles, with 43% completing all six planned cycles.
- 39% of patients discontinued IP treatment due to drug-related toxicities (22%) or administration-related complications (17%).
Conclusions:
- The study demonstrates the feasibility and practicality of IP chemotherapy for ovarian cancer in Australia.
- Key lessons learned from initial experiences are highlighted, informing future practice.

