Search Results - "Antill, Yoland"
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Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles
Published in PLoS genetics (01-09-2012)“…Despite intensive efforts using linkage and candidate gene approaches, the genetic etiology for the majority of families with a multi-generational breast…”
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Exercise as a diagnostic and therapeutic tool for the prevention of cardiovascular dysfunction in breast cancer patients
Published in European journal of preventive cardiology (01-02-2019)“…Background Anthracycline chemotherapy may be associated with decreased cardiac function and functional capacity measured as the peak oxygen uptake during…”
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Clinical activity of durvalumab for patients with advanced mismatch repair-deficient and repair-proficient endometrial cancer. A nonrandomized phase 2 clinical trial
Published in Journal for immunotherapy of cancer (01-06-2021)“…BackgroundIn this study, we assessed the activity of durvalumab, an antibody to programmed death ligand-1, in two cohorts of women with advanced endometrial…”
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Cancer Risks for MLH1 and MSH2 Mutation Carriers
Published in Human mutation (01-03-2013)“…ABSTRACT We studied 17,576 members of 166 MLH1 and 224 MSH2 mutation‐carrying families from the Colon Cancer Family Registry. Average cumulative risks of…”
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Breast cancer polygenic risk scores: a 12-month prospective study of patient reported outcomes and risk management behavior
Published in Genetics in medicine (01-12-2021)“…Purpose To prospectively assess patient reported outcomes and risk management behavior of women choosing to receive (receivers) or decline (decliners) their…”
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Pilot study of an online training program to increase genetic literacy and communication skills in oncology healthcare professionals discussing BRCA1/2 genetic testing with breast and ovarian cancer patients
Published in Familial cancer (01-04-2022)“…The increasing use of genetic testing for BRCA1/2 and other pathogenic variants in the management of women with breast and ovarian cancer necessitates…”
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Enhanced Toxicity With Trastuzumab Emtansine And Concurrent Adjuvant Radiotherapy: Non-Consecutive Case Series
Published in Breast (Edinburgh) (01-04-2023)Get full text
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Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers
Published in JNCI : Journal of the National Cancer Institute (03-02-2010)“…Background Germline mutations in MSH6 account for 10%–20% of Lynch syndrome colorectal cancers caused by hereditary DNA mismatch repair gene mutations. Because…”
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Exercise as a diagnostic and therapeutic tool for preventing cardiovascular morbidity in breast cancer patients- the BReast cancer EXercise InTervention (BREXIT) trial protocol
Published in BMC cancer (14-07-2020)“…Anthracycline chemotherapy (AC) is an efficacious (neo) adjuvant treatment for early-stage breast cancer (BCa), but is associated with an increased risk of…”
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Denosumab: Prevention and management of hypocalcemia, osteonecrosis of the jaw and atypical fractures
Published in Asia-Pacific journal of clinical oncology (01-08-2017)“…Denosumab, a bone‐modifying agent, reduces the risk of skeletal‐related events in patients with bone metastases from solid tumors and is generally well…”
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A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Published in Journal of translational medicine (26-04-2023)“…Routine screening of tumors for DNA mismatch repair (MMR) deficiency (dMMR) in colorectal (CRC), endometrial (EC) and sebaceous skin (SST) tumors leads to a…”
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Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history
Published in European journal of human genetics : EJHG (01-07-2018)“…In patients with early breast cancer, personal and tumour characteristics other than family history are increasingly used to prompt genetic testing to guide…”
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Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial
Published in Genetics in medicine (01-04-2017)“…Increasingly, women newly diagnosed with breast cancer are being offered treatment-focused genetic testing (TFGT). As the demand for TFGT increases,…”
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PARAGON (ANZGOG-0903): a phase 2 study of anastrozole in asymptomatic patients with estrogen and progesterone receptor-positive recurrent ovarian cancer and CA125 progression
Published in Journal of gynecologic oncology (01-09-2019)“…A subset of patients with recurrent ovarian cancer (ROC) may benefit from antiestrogen therapy with higher response rates reported in tumors that are strongly…”
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Identifying primary and secondary MLH1 epimutation carriers displaying low-level constitutional MLH1 methylation using droplet digital PCR and genome-wide DNA methylation profiling of colorectal cancers
Published in Clinical epigenetics (03-06-2023)“…MLH1 epimutation is characterised by constitutional monoallelic MLH1 promoter hypermethylation, which can cause colorectal cancer (CRC). Tumour molecular…”
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Lynch syndrome and cervical cancer
Published in International journal of cancer (01-12-2015)“…Carriers of germline mutations in DNA mismatch repair (MMR) genes are at increased risk of several cancers including colorectal and gynecologic cancers (Lynch…”
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Therapeutic options for mucinous ovarian carcinoma
Published in Gynecologic oncology (01-03-2020)“…Mucinous ovarian carcinoma (MOC) is an uncommon ovarian cancer histotype that responds poorly to conventional chemotherapy regimens. Although long overall…”
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Exercise Attenuates Cardiotoxicity of Anthracycline Chemotherapy Measured by Global Longitudinal Strain
Published in JACC CardioOncology (01-12-2019)Get full text
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Gene Methylation in Breast Ductal Fluid from BRCA1 and BRCA2 Mutation Carriers
Published in Cancer epidemiology, biomarkers & prevention (01-01-2010)“…Purpose: Genomic alterations (including gene hypermethylation) are likely to precede the phenotypic changes associated with breast tumorigenesis. From a…”
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Loss of Heterozygosity at the BRCA2 Locus Detected by Multiplex Ligation-Dependent Probe Amplification is Common in Prostate Cancers from Men with a Germline BRCA2 Mutation
Published in Clinical cancer research (15-05-2008)“…Purpose: Prostate cancer risk is increased for men carrying a pathogenic germline mutation in BRCA2 , and perhaps BRCA1. Our primary aim was to test for loss…”
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