Investigator

Leon Foster

Visiting Medical Officer · Canberra Health Services, Gynaecology Oncology

LFLeon Foster
Papers(3)
The use of intraperit…The socioeconomic gra…The utilisation of se…
Collaborators(6)
Alison BrandMichael BurlingPaul HarnettStephen J. RobsonAdrienne KirbyChristina Girgis
Institutions(5)
Royal Zoological Soci…NHMRC Clinical Trials…The University Of Syd…Act GovernmentWestmead Hospital

Papers

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

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.

The socioeconomic gradient in mortality from ovarian, cervical, and endometrial cancer in Australian women, 2001–2018: A population‐based study

BackgroundSocio‐economic (SE) status is closely linked to health status and the mechanisms of this association are complex. One important adverse effect of SE disadvantage is vulnerability to cancer and cancer is a major cause of morbidity and mortality in Australia.AimsWe aimed to estimate the effect of SE status on mortality rates from ovarian, cervical, and endometrial cancer.Materials and MethodsNational mortality data were obtained from the Australian Bureau of Statistics (ABS) for the calendar years from 2001 to 2018, inclusive. Individual deaths were grouped by the ABS Index of Relative Socio‐economic Advantage and Disadvantage. Population data were obtained to provided denominators allowing calculation of mortality rates (deaths per 100 000 women aged 30–79 years). Statistical analyses performed included tabulating point‐estimates of mortality rates and their changes over time and modelling the trends of rates using maximum likelihood method.ResultsAge‐standardised mortality rates for ovarian and cervical cancer fell over the study period but increased for endometrial cancer. There was clear evidence of a SE gradient in the mortality rate for all three cancers. This SE gradient increased over the study period for ovarian and cervical cancer but remained unchanged for endometrial cancer.ConclusionsWomen at greater SE disadvantage have higher rates of death from the commonest gynaecological cancers and this gradient has not reduced over the last two decades. After the COVID‐19 pandemic efforts must be redoubled to ensure that Australians already at risk of ill health do not face even greater risks because of their circumstances.

The utilisation of sentinel lymph node biopsy for endometrial cancer in Australia and New Zealand

AimsThe aim of this study was to identify to what extent the sentinel lymph node (SLN) technique is utilised by gynaecological oncologists in Australia and New Zealand, identifying the techniques used, any barriers to uptake, and management of isolated tumour cells (ITCs) and micrometastases.Materials and methodsWe conducted an online survey of all practising gynaecological oncologists in Australia and New Zealand. They were asked whether they utilised SLN biopsy and in what circumstances, how they managed non‐mapping and how their multidisciplinary team managed small volume disease. Those who did not were asked to identify their concerns with the procedure, reasons for non‐uptake and their alternate technique.ResultsWe surveyed 63 gynaecological oncologists of whom 59 were practising, and 48 (81%) responded. Six members (11%) do not utilise SLN biopsy, and 42 (89%) do. Areas where clinicians differ in practice are those areas that are most controversial and include the use of SLN biopsy in complex atypical hyperplasia, the management of ITCs and micrometastases and procedures on unilateral or bilateral non‐mapping. Those who do not utilise the technique cite concerns about the false‐negative rate, equipment and training issues.ConclusionsThe utilisation of SLN biopsy in endometrial cancer is well established in Australia and New Zealand, with similar practices and concerns to those of other international groups.

7Works
3Papers
6Collaborators

Positions

2023–

Visiting Medical Officer

Canberra Health Services · Gynaecology Oncology

2020–

Fellow

Westmead Hospital · Gynaecology Oncology

2016–

Researcher

ACT Health

2010–

Researcher

Canberra Hospital

Education

2015

Masters of Public Health

University of Queensland

2009

Bachelor of Medicine / Bachelor of Surgery

Australian National University

1999

Bachelor of Arts

University of New South Wales