Plasma ESR1 Mutations and the Treatment of Estrogen Receptor-Positive Advanced Breast Cancer.
By C. Fribbens, B. O’Leary, L. Kilburn, S. Hrebien, I. Garcia-Murillas, M. Beaney, M. Cristofanilli, F. André, S. Loi, S. Loibl and 7 more. Journal of Clinical Oncology, 2016
639 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics, Pulmonary and Respiratory Medicine
View Paper: https://www.semanticscholar.org/paper/ad83ee94ec2d007eae96c0e335fc7f77aa46a7e3
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In Cancer Research
In Genetics
In Pulmonary and Respiratory Medicine
Citations in the corpus
- Recommendations for the use of next-generation sequencing (NGS) for patients with metastatic cancers: A report from the ESMO Precision Medicine Working Group. (2020, background): “ESR1 mutations occur in around 20% of patients previously treated with aromatase inhibitors and are associated with response to selective estrogen receptor degraders.(74) Nevertheless, these data are preliminary and cannot be used in daily practice.”
- De-escalating and escalating treatments for early-stage breast cancer: the St. Gallen International Expert Consensus Conference on the Primary Therapy of Early Breast Cancer 2017 (2018, background): “Molecular mechanisms of resistance to therapy Activating mutations in the estrogen receptor ESR1 gene arise in 30%–40% of recurrences on AI therapy and likely account for resistance to AI treatment in those cases [81].”
- Overcoming Endocrine Resistance in Breast Cancer (2020, positive): “The prevalence of ESR1 mutations in plasma ctDNA in similar populations is even higher (Fribbens et al., 2016; Schiavon et al., 2015).”
- 5th ESO-ESMO international consensus guidelines for advanced breast cancer (ABC 5) (2020, background): “74).(87) Despite promising preclinical data and statistical trends, the ESCAT scale for ESR1 mutations is tier II.”
- The Genomic Landscape of Endocrine-Resistant Advanced Breast Cancers (2018, background): “On the other hand, and reflecting the impact of prior therapy, ligand binding domain mutations in ESR1 were present in 18% of HRHER2 patients whose sequenced tumor specimens were collected after endocrine therapy (n = 128 of 692) (Chandarlapaty et al., 2016; Fribbens et al., 2016; Robinson et al., 2”