Everolimus in hormone receptor–positive advanced breast cancer: Targeting receptor-based mechanisms of resistance
The Breast, ISSN: 0960-9776, Vol: 22, Issue: 4, Page: 405-410
2013
- 17Citations
- 25Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations17
- Citation Indexes17
- 17
- CrossRef11
- Captures25
- Readers25
- 25
Review Description
Although patients with hormone receptor (HR)–positive breast cancer are successfully treated with endocrine therapy, many tumors go on to develop resistance to these agents. Studies have determined that mechanisms of resistance to endocrine therapy are quite complex and can involve a multitude of signal transduction pathways, either through direct association with the estrogen receptor or through cross-talk with other pathways. Preclinical studies have suggested the therapeutic importance of the mammalian target of rapamycin (mTOR) pathway and that inhibiting this pathway may restore sensitivity to endocrine therapy. The oral mTOR inhibitor everolimus has been extensively studied for breast cancer. Clinical studies suggest that everolimus in combination with endocrine therapy improves progression-free survival and is well tolerated. A combined approach, targeting both mTOR signal transduction and the HR pathways, promises to take clinical research in a new direction for the treatment of HR-positive advanced breast cancer.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0960977613000349; http://dx.doi.org/10.1016/j.breast.2013.02.003; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84879782716&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/23499266; https://linkinghub.elsevier.com/retrieve/pii/S0960977613000349; https://dx.doi.org/10.1016/j.breast.2013.02.003
Elsevier BV
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