The use of intraperitoneal chemotherapy for advanced ovarian cancer – The experience of a tertiary referral centre

Author:

Foster Leon12ORCID,Girgis Christina3ORCID,Kirby Adrienne4ORCID,Harnett Paul35ORCID,Brand Alison15ORCID

Affiliation:

1. Department of Gynaecology Oncology Westmead Hospital Sydney New South Wales Australia

2. The University of New South Wales Sydney New South Wales Australia

3. Crown Princess Mary Cancer Centre Westmead Hospital Sydney New South Wales Australia

4. Clinical Trials Centre, National Health and Medical Research Council University of Sydney Sydney New South Wales Australia

5. School of Medicine University of Sydney Sydney New South Wales Australia

Abstract

BackgroundPlatinum‐based chemotherapy is the backbone of the medical management of ovarian cancer. The dose, route and timing of treatment are ongoing areas of debate. Intraperitoneal (IP) chemotherapy is an alternative delivery method treatment to the conventional intravenous (IV) route for patients with epithelial ovarian cancer, with efficacy supported by Level 1 evidence.AimsTo compare the outcomes and feasibility of IP to IV delivery of platinum‐based chemotherapy in patients with advanced epithelial ovarian cancer.Materials and MethodsIn a single institution, patients receiving adjuvant chemotherapy (IP and IV) for Stages III and IV epithelial ovarian cancer over the period January 2006–December 2018 were identified through a prospectively maintained database. All patients with an IP port inserted were included. A control group of patients treated with IV chemotherapy was created using criteria identified during the study and in the randomised trials that tested IP chemotherapy. Assessments were made for relapse‐free survival (RFS) and overall survival (OS) for each cohort.ResultsA total of 639 patients received adjuvant chemotherapy (73 IP and 566 IV) during the study period. Both the IP group and matched IV control group (65 patients) had a median RFS of 26 months. The median OS in the IP group was 63.9 months, and in the IV group was 57.2 months. At ten years, a significantly higher proportion of patients were alive in the IP group cohort (16% vs 3%, relative risk 5.5, 95% CI 1.29–24, P = 0.012). IP chemotherapy was well tolerated by our cohort. In the IP group, 73% had four or more IP cycles and 99% received six or more cycles of chemotherapy.ConclusionsOur cohort had a high rate of completion of IP chemotherapy with excellent rates of completion of six cycles of any treatment. The RFS and OS in the IP chemotherapy group were comparable to each other and reflected those in the published literature. A significantly higher proportion of patients in the IP cohort were alive at ten years than in the IV cohort.

Publisher

Wiley

Subject

Obstetrics and Gynecology,General Medicine

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1. Editor‐in‐Chief's introduction to ANZJOG 64 (3);Australian and New Zealand Journal of Obstetrics and Gynaecology;2024-06

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