Michael Friedlander
迈克尔·弗里德兰德
MB ChB, PhD, FRACP
Professor of Medical Oncology, Prince of Wales Clinical School, UNSW; Medical Oncologist, Prince of Wales Hospital; former Chair, ANZGOG (Australia New Zealand Gynaecological Oncology Group)新南威尔士大学威尔士亲王临床学院医学肿瘤学教授;威尔士亲王医院医学肿瘤科医生;前澳大利亚新西兰妇科肿瘤组主席
👥Biography 个人简介
Michael Friedlander, MB ChB, PhD, FRACP is Professor of Medical Oncology at Prince of Wales Clinical School, University of New South Wales, and an attending medical oncologist at Prince of Wales Hospital in Sydney. He is one of Australia's most distinguished gynecologic oncologists and a globally influential figure in ovarian cancer clinical research, having served as former chair of the Australia New Zealand Gynaecological Oncology Group (ANZGOG) and co-chair of the Gynecologic Cancer InterGroup (GCIG). Professor Friedlander has been a principal investigator or key contributor to some of the most important ovarian cancer clinical trials of the past three decades, including the ICON series, SOLO-1 and SOLO-2, AGO-OVAR series, and multiple ANZGOG-led studies. He has made foundational contributions to understanding the clinical and biological behavior of BRCA1/2-mutant ovarian cancer — demonstrating superior chemosensitivity, distinct natural history, and exceptional responses to PARP inhibitor therapy in BRCA-mutant patients — contributing to the systematic integration of germline BRCA testing into ovarian cancer clinical practice. Professor Friedlander has led Australia's national framework for BRCA testing and genetic counseling in ovarian cancer patients and their families, and has contributed to GCIG consensus recommendations on clinical trial endpoint selection, response criteria, and quality-of-life measurement in ovarian cancer trials. He has authored over 250 peer-reviewed publications and is a founding contributor to patient advocacy and survivorship programs in gynecologic oncology in Australasia.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
BRCA-Mutant Ovarian Cancer — Clinical Characterization and PARP Inhibitor Response
Made seminal contributions to characterizing the distinct clinical behavior of BRCA1/2-mutant ovarian cancer, including superior response to platinum-based chemotherapy, longer platinum-free intervals, and exceptional sensitivity to PARP inhibitors. Led and contributed to landmark studies — including the ICON series (ICON1, ICON3, ICON5, ICON6, ICON7) — establishing the prognostic value of BRCA mutation status and platinum sensitivity. Contributed to pivotal analyses demonstrating BRCA-mutant patients' exceptional benefit from olaparib maintenance in Study 19, SOLO-1, and SOLO-2, helping define this population as a paradigmatic precision oncology cohort.
ANZGOG Cooperative Group Leadership and Trial Infrastructure
Served as founding member and chair of ANZGOG, building Australia and New Zealand's national cooperative gynecologic oncology research infrastructure from the ground up. Under his leadership, ANZGOG activated and completed landmark phase II and III trials including ANZGOG-0902 (carboplatin dose-dense scheduling), and activated multiple GCIG and ENGOT-partnered trials including ICON series and SOLO studies as Australian principal sites. Created the national patient registry and biobank infrastructure that underpins translational ovarian cancer research in Australia and contributed to GCIG's global trial harmonization.
Germline BRCA Testing and Genetic Counseling Integration
Championed systematic germline BRCA1/2 testing as standard of care for all newly diagnosed ovarian cancer patients in Australia, co-authoring national clinical practice guidelines that predate and influenced international guideline adoption. Led studies demonstrating that BRCA testing performed by oncologists at the time of ovarian cancer diagnosis with streamlined genetic counseling achieves higher uptake than traditional genetics referral pathways, establishing the "mainstreaming" approach to ovarian cancer BRCA testing that has been adopted in multiple countries.
Platinum-Sensitive Recurrent Ovarian Cancer — Treatment Sequencing
Contributed extensively to the evidence base for platinum re-treatment, non-platinum salvage regimens, and PARP inhibitor sequencing in platinum-sensitive recurrent ovarian cancer. Participated in ICON4, CALYPSO (carboplatin-pegylated liposomal doxorubicin versus carboplatin-paclitaxel), and multiple ANZGOG salvage therapy studies, providing comparative efficacy and quality-of-life data informing contemporary treatment sequencing algorithms and demonstrating the importance of platinum-free interval as a continuous rather than dichotomous predictor of re-treatment benefit.
Representative Works 代表性著作
Paclitaxel plus Platinum-Based Chemotherapy versus Conventional Platinum-Based Chemotherapy in Women with Relapsed Ovarian Cancer (ICON4)
The Lancet (2003)
ICON4 landmark trial demonstrating paclitaxel-platinum superiority over platinum alone in platinum-sensitive recurrent ovarian cancer, establishing the doublet standard for recurrent disease.
Carboplatin and Pegylated Liposomal Doxorubicin versus Carboplatin and Paclitaxel in Platinum-Sensitive Ovarian Cancer: the CALYPSO Trial
Journal of the National Cancer Institute (2010)
CALYPSO phase III trial demonstrating non-inferiority of carboplatin-PLD versus carboplatin-paclitaxel in platinum-sensitive recurrent ovarian cancer with a superior toxicity profile.
Maintenance Olaparib in Patients with Newly Diagnosed Advanced Ovarian Cancer (SOLO-1)
New England Journal of Medicine (2018)
SOLO-1 Australian co-investigator; landmark trial demonstrating 70% risk reduction in disease progression with frontline olaparib maintenance in BRCA-mutant ovarian cancer.
"Mainstreaming" BRCA Testing in Women with Ovarian Cancer: A Feasibility Study
Journal of Clinical Oncology (2017)
Demonstration that oncologist-led BRCA testing at ovarian cancer diagnosis with streamlined genetic counseling achieves high uptake, establishing the "mainstreaming" model widely adopted internationally.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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