![]() | Michael Leonard FriedlanderDepartment of Medical Oncology, Prince of Wales Hospital and Prince of Wales Clinical School, UNSW, Sydney, New South Wales, Australia. Electronic address: ... |
KOL Resume for Michael Leonard Friedlander
Year | |
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2022 | Department of Medical Oncology, Prince of Wales Hospital and Prince of Wales Clinical School, UNSW, Sydney, New South Wales, Australia. Electronic address: Prince of Wales Clinical School, UNSW, Sydney, Australia |
2021 | Department of Medical Oncology, Prince of Wales Hospital, Barker St. Randwick, New South Wales, Australia. University of New South Wales Clinical School, Prince of Wales Hospital, Randwick, Australia |
2020 | Royal Hospital for Women, Randwick, NSW, Australia University of New South Wales Clinical School, Prince of Wales Hospital |
2019 | Department of Medical Oncology, Nelune Comprehensive Cancer Centre, University of New South Wales Clinical School, Prince of Wales Hospital, Sydney, NSW, Australia. Electronic address: Prince of Wales Hospital, Randwick. Nelune Comprehensive Cancer Centre, Royal Hospital for Women, Sydney, New South Wales, Australia |
Michael Leonard Friedlander: Influence Statistics
Concept | World rank |
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women highstable | #1 |
6 cycles arm | #1 |
exploratory populations population | #1 |
depression female genes | #1 |
positive retroperitoneal lymph | #1 |
brca1m | #1 |
improvement consecutive scores | #1 |
clinical benefit life | #1 |
vcp orr | #1 |
fertilityrelated menopauserelated | #1 |
firstline chemotherapy measure | #1 |
balance deficits p001 | #1 |
ltdfs≥10 years | #1 |
ucs lms cohort | #1 |
firstline chemotherapy mosts26 | #1 |
symptoms firstline chemotherapy | #1 |
totaldc | #1 |
recovery cycle infusion | #1 |
neurotoxic treatment oxaliplatin | #1 |
fertility decisional conflict | #1 |
rp exploration pfs | #1 |
95 bevct | #1 |
male carboplatin | #1 |
tropomyosin31 | #1 |
trials orr | #1 |
p0001 higher mgps | #1 |
aim stage | #1 |
roc female humans | #1 |
pps roc | #1 |
population concordance rates | #1 |
hgsoc brca mutation | #1 |
surgical spill | #1 |
women epithelial ovarian | #1 |
cohorts primary endpoints | #1 |
patients ltdfs | #1 |
ddcp groups | #1 |
characteristics upper limit | #1 |
survival higher optimism | #1 |
chemotherapy prroc | #1 |
median pfs ddcp | #1 |
bleomycin dosing | #1 |
randomization pfs | #1 |
ppc epithelial chemotherapy | #1 |
– analysis | #1 |
data estimation models | #1 |
impact reproductive function | #1 |
twoinfive women | #1 |
questionnaires attitude phase | #1 |
timevarying cox model | #1 |
maintenance pazopanib placebo | #1 |
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Prominent publications by Michael Leonard Friedlander
Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
[ PUBLICATION ]
Importance: The clinical management of BRCA1 and BRCA2 mutation carriers requires accurate, prospective cancer risk estimates.
Objectives: To estimate age-specific risks of breast, ovarian, and contralateral breast cancer for mutation carriers and to evaluate risk modification by family cancer history and mutation location.
Design, Setting, and Participants: Prospective cohort study of 6036 BRCA1 and 3820 BRCA2 female carriers (5046 unaffected and 4810 with breast or ovarian cancer or ...
Known for Breast Cancer | Mutation Carriers | Brca1 95 | 80 Years | Risk Age |
BACKGROUND: Olaparib, a poly(ADP-ribose) polymerase (PARP) inhibitor, has previously shown efficacy in a phase 2 study when given in capsule formulation to all-comer patients with platinum-sensitive, relapsed high-grade serous ovarian cancer. We aimed to confirm these findings in patients with a BRCA1 or BRCA2 (BRCA1/2) mutation using a tablet formulation of olaparib.
METHODS: This international, multicentre, double-blind, randomised, placebo-controlled, phase 3 trial evaluated olaparib ...
Known for Patients Olaparib | 3 Trial | Relapsed Ovarian | Brca1 Genes | Maintenance Therapy |
BACKGROUND: Rucaparib, a poly(ADP-ribose) polymerase inhibitor, has anticancer activity in recurrent ovarian carcinoma harbouring a BRCA mutation or high percentage of genome-wide loss of heterozygosity. In this trial we assessed rucaparib versus placebo after response to second-line or later platinum-based chemotherapy in patients with high-grade, recurrent, platinum-sensitive ovarian carcinoma.
METHODS: In this randomised, double-blind, placebo-controlled, phase 3 trial, we recruited ...
Known for Patients Placebo | Ovarian Carcinoma | Platinum Therapy | 3 Trial | Rucaparib Maintenance |
BACKGROUND: In patients with platinum-sensitive recurrent serous ovarian cancer, maintenance monotherapy with the PARP inhibitor olaparib significantly improves progression-free survival versus placebo. We assessed the effect of maintenance olaparib on overall survival in patients with platinum-sensitive recurrent serous ovarian cancer, including those with BRCA1 and BRCA2 mutations (BRCAm).
METHODS: In this randomised, placebo-controlled, double-blind, phase 2 trial involving 82 sites ...
Known for Serous Ovarian | Olaparib Maintenance | Placebo Patients | Sensitive Recurrent | 2 Years |
Olaparib combined with chemotherapy for recurrent platinum-sensitive ovarian cancer: a randomised phase 2 trial
[ PUBLICATION ]
BACKGROUND: The poly(ADP-ribose) polymerase inhibitor olaparib has shown antitumour activity in patients with platinum-sensitive, recurrent, high-grade serous ovarian cancer with or without BRCA1 or BRCA2 mutations. The aim of this study was to assess the efficacy and tolerability of olaparib in combination with chemotherapy, followed by olaparib maintenance monotherapy, versus chemotherapy alone in patients with platinum-sensitive, recurrent, high-grade serous ovarian cancer.
METHODS: ...
Known for Chemotherapy Patients | Sensitive Ovarian | Recurrent Platinum | Paclitaxel Carboplatin | Local Neoplasms |
BACKGROUND: BRCA1 or BRCA2-mutated breast cancers are sensitive to poly(ADP-ribose) polymerase (PARP) inhibitors and platinum agents owing to deficiency in homologous recombination repair of DNA damage. In this trial, we compared veliparib versus placebo in combination with carboplatin and paclitaxel, and continued as monotherapy if carboplatin and paclitaxel were discontinued before progression, in patients with HER2-negative advanced breast cancer and a germline BRCA1 or BRCA2 ...
Known for Carboplatin Paclitaxel | Veliparib Placebo | Advanced Breast | Patients Control | Brca1 Genes |
BACKGROUND: Maintenance monotherapy with the PARP inhibitor olaparib significantly prolonged progression-free survival (PFS) versus placebo in patients with platinum-sensitive recurrent serous ovarian cancer. We aimed to explore the hypothesis that olaparib is most likely to benefit patients with a BRCA mutation.
METHODS: We present data from the second interim analysis of overall survival and a retrospective, preplanned analysis of data by BRCA mutation status from our randomised, ...
Known for Patients Olaparib | Serous Ovarian | Randomised Phase | Brca Mutation | 2 Trial |
BACKGROUND: Olaparib, a novel, orally active poly(ADP-ribose) polymerase (PARP) inhibitor, induced synthetic lethality in BRCA-deficient cells. A maximum tolerated dose and initial signal of efficacy in BRCA-deficient ovarian cancers have been reported. We therefore assessed the efficacy, safety, and tolerability of olaparib alone in women with BRCA1 or BRCA2 mutations and advanced breast cancer.
METHODS: Women (aged >or=18 years) with confirmed BRCA1 or BRCA2 mutations and recurrent, ...
Known for Brca2 Mutations | Advanced Breast Cancer | Patients Brca1 | Olaparib Women | Female Genes |
BACKGROUND: Angiogenesis is a validated clinical target in advanced epithelial ovarian cancer. Cediranib is an oral antiangiogenic vascular endothelial growth factor receptor 1-3 inhibitor that has shown antitumour activity in recurrent ovarian cancer. We assessed efficacy and safety of cediranib in combination with platinum-based chemotherapy and as continued maintenance treatment in patients with first relapse of platinum-sensitive ovarian cancer.
METHODS: In this randomised, ...
Known for Ovarian Cancer | 3 Trial | Chemotherapy Cediranib | Arm Maintenance | Local Neoplasms |
BACKGROUND: Independent validation is essential to justify use of models of breast cancer risk prediction and inform decisions about prevention options and screening. Few independent validations had been done using cohorts for common breast cancer risk prediction models, and those that have been done had small sample sizes and short follow-up periods, and used earlier versions of the prediction tools. We aimed to validate the relative performance of four commonly used models of breast ...
Known for Breast Cancer | Validation Study | Boadicea Ibis | Brcapro Bcrat | 10 Years |
PURPOSE: Olaparib (AZD2281), an orally active poly (ADP-ribose) polymerase inhibitor that induces synthetic lethality in BRCA1- or BRCA2-deficient cells, has shown promising clinical efficacy in nonrandomized phase II trials in patients with ovarian cancer with BRCA1 or BRCA2 deficiency. We assessed the comparative efficacy and safety of olaparib and pegylated liposomal doxorubicin (PLD) in this patient population.
PATIENTS AND METHODS: In this multicenter, open-label, randomized, phase ...
Known for Brca2 Mutations | Ovarian Cancer | Brca1 Genes | Multicenter Study | Efficacy Safety |
BACKGROUND: Olaparib is a novel, orally active poly(ADP-ribose) polymerase (PARP) inhibitor that induces synthetic lethality in homozygous BRCA-deficient cells. We aimed to assess the efficacy and safety of olaparib for treatment of advanced ovarian cancer in patients with BRCA1 or BRCA2 mutations.
METHODS: In this international, multicentre, phase 2 study, we enrolled two sequential cohorts of women (aged >or=18 years) with confirmed genetic BRCA1 or BRCA2 mutations, and recurrent, ...
Known for Brca2 Mutations | Patients Olaparib | Recurrent Ovarian Cancer | Grade 3 | 2 Study |
BACKGROUND: Most women with newly diagnosed advanced ovarian cancer have a relapse within 3 years after standard treatment with surgery and platinum-based chemotherapy. The benefit of the oral poly(adenosine diphosphate-ribose) polymerase inhibitor olaparib in relapsed disease has been well established, but the benefit of olaparib as maintenance therapy in newly diagnosed disease is uncertain.
METHODS: We conducted an international, randomized, double-blind, phase 3 trial to evaluate the ...
Known for Maintenance Olaparib | Advanced Ovarian | Brca1 Genes | Disease Progression Death | 3 Years |
BACKGROUND: In the phase 3 SOLO2 trial (ENGOT Ov-21), maintenance therapy with olaparib tablets significantly prolonged progression-free survival (primary endpoint) compared with placebo in patients with a germline BRCA1 or BRCA2 (BRCA1/2) mutation and platinum-sensitive, relapsed ovarian cancer who had received two or more lines of previous chemotherapy. The most common subjective adverse effects included fatigue, nausea, and vomiting, which were typically low grade and self-limiting. ...
Known for Olaparib Placebo | Life Hrqol | Phase 3 | Primary Endpoint | Centred Outcomes |
Anti-Müllerian hormone serum concentrations of women with germline BRCA1 or BRCA2 mutations
[ PUBLICATION ]
STUDY QUESTION: Do women with ITALIC! BRCA1 or ITALIC! BRCA2 mutations have reduced ovarian reserve, as measured by circulating anti-Müllerian hormone (AMH) concentration?
SUMMARY ANSWER: Women with a germline mutation in ITALIC! BRCA1 have reduced ovarian reserve as measured by AMH.
WHAT IS KNOWN ALREADY: The DNA repair enzymes encoded by ITALIC! BRCA1 and ITALIC! BRCA2 are implicated in reproductive aging. Circulating AMH is a biomarker of ovarian reserve and hence reproductive ...
Known for Brca2 Mutations | Ovarian Reserve | Mutation Carriers | Reproductive Lifespan | Müllerian Hormone |
Key People For Ovarian Cancer
Michael Leonard Friedlander:Expert Impact
Concepts for whichMichael Leonard Friedlanderhas direct influence:Ovarian cancer, Breast cancer, Maintenance olaparib, Brca1 genes, Brca mutation, Brca2 mutation carriers.
Michael Leonard Friedlander:KOL impact
Concepts related to the work of other authors for whichfor which Michael Leonard Friedlander has influence:Ovarian cancer, Parp inhibitors, Genetic testing, Flow cytometry, Dna ploidy, Fertility preservation, Neoadjuvant chemotherapy.
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