Clare Scott
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Recent Grants
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Accelerating translational outcomes based on super-responders from the SOLACE2 trial of immunotherapy priming in ovarian cancer
Open Date: 2022-01-01
Close Date: 2024-01-01
Grant: Open
Ovarian Cancers Research Program: Matching a woman’s ovarian cancer to new treatments
Open Date: 2022-01-01
Close Date: 2027-01-01
Grant: Close
Super-Responders and Super-Survivors – how to dramatically improve cancer outcomes
Open Date: 2021-09-14
Close Date:
Grant: Close
WEHI Stafford Fox Rare Cancer Program: Changing the future for patients with rare cancers
Open Date: 2021-01-01
Close Date: 2026-01-01
Grant: Close
Multiple primary tumours: immune response and metastasis prevention
Open Date: 2020-01-01
Close Date: 2021-01-01
Articles (10)
Year:
2025
Year:
2024
Year:
2024
Year:
2024
Year:
2024
Year:
2023
Aim To catalogue and compare the pattern of metastatic disease in germline BRCA1/2 pathogenic mutation carriers and non‐carriers with breast, ovarian and prostate cancer from a rapid autopsy programme. Methods and results The number of metastases in the major body systems and the proportion of participants with metastases were documented in 50 participants (19 germline mutation carriers). Analysis was conducted on the participants’ pattern of disease for the different cancers and mutation subgroups. The four commonly affected organ systems were the digestive (liver only) (82%), respiratory (76%), gastrointestinal (65%) and reticuloendothelial (42%). There were significant differences in the pattern of metastatic breast cancer in BRCA1/2 germline carriers compared with non‐carriers. Breast cancer carriers had significantly fewer organ systems involved (median n = 3, range = 1–3) compared with non‐carriers (median n = 9, range = 1–7) ( P = 0.03). BRCA1/2 carriers with ovarian carcinomas had significantly more organ systems with metastatic carcinoma (median n = 10, range = 3–8) than non‐carriers (median n = 5, range = 3–5) ( P < 0.001). There were no significant differences in the number of involved systems in BRCA2 carriers compared with non‐carriers with prostate cancer ( P = 1.0). There was an absence of locoregional disease (6.5%) compared with distant disease (93.5%) among the three cancer subtypes ( P < 0.001). The majority of metastatic deposits (97%) collected during the autopsy were identified by recent diagnostic imaging. Conclusion Even though a major limitation of this study is that our numbers are small, especially in the breast cancer carrier group, the metastatic patterns of breast and ovarian cancers may be impacted by BRCA1/2 carrier status, suggesting that tumours derived from patients with these mutations use different mechanisms of dissemination. The findings may focus clinical diagnostic imaging for monitoring metastases where whole‐body imaging resources are scant.
Year:
2023
Year:
2023
Year:
2022
Year:
2022
Collaborators (6)
Stephen Fox
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Matthew Wakefield
University of Melbourne
Jonathan Ledermann
University College London
John R. Zalcberg
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Mansoor Mirza
Chief Oncologist
Rigshospitalet
Sarah (Sally) J Lord
Associate Professor, Research
The University of Notre Dame Australia
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