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Therapies for the Treatment of Advanced/Metastatic Estrogen Receptor-Positive Breast Cancer: Current Situation and Future Directions

dc.contributor.authorRej, Rohan Kalyan
dc.contributor.authorRoy, Joyeeta
dc.contributor.authorAllu, Srinivasa Rao
dc.date.accessioned2024-02-01T01:10:13Z
dc.date.available2024-02-01T01:10:13Z
dc.date.issued2024-01-27
dc.identifier.issn2072-6694
dc.identifier.urihttps://hdl.handle.net/2027.42/192163
dc.description.abstract<jats:p>The hormone receptor-positive (HR+) type is the most frequently identified subtype of breast cancer. HR+ breast cancer has a more positive prognosis when compared to other subtypes, such as human epidermal growth factor protein 2-positive disorder and triple-negative disease. The advancement in treatment outcomes for advanced HR+ breast cancer has been considerably elevated due to the discovery of cyclin-dependent kinase 4/6 inhibitors and their combination effects with endocrine therapy. However, despite the considerable effectiveness of tamoxifen, a selective estrogen receptor modulator (SERMs), and aromatase inhibitors (AI), the issue of treatment resistance still presents a significant challenge for HR+ breast cancer. As a result, there is a focus on exploring new therapeutic strategies such as targeted protein degradation and covalent inhibition for targeting ERα. This article discusses the latest progress in treatments like oral selective ER degraders (SERDs), complete estrogen receptor antagonists (CERANs), selective estrogen receptor covalent antagonists (SERCAs), proteolysis targeting chimera (PROTAC) degraders, and combinations of CDK4/6 inhibitors with endocrine therapy. The focus is specifically on those compounds that have transitioned into phases of clinical development.</jats:p>
dc.languageen
dc.publisherMDPI AG
dc.titleTherapies for the Treatment of Advanced/Metastatic Estrogen Receptor-Positive Breast Cancer: Current Situation and Future Directions
dc.typeArticle
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/192163/2/cancers-16-00552-v2 (1).pdf
dc.identifier.doi10.3390/cancers16030552
dc.identifier.doihttps://dx.doi.org/10.7302/22163
dc.identifier.sourceCancers
dc.description.versionPublished online
dc.date.updated2024-02-01T01:10:09Z
dc.identifier.orcid0000-0003-0904-9137
dc.identifier.orcid0000-0001-9178-2578
dc.identifier.volume16
dc.identifier.issue3
dc.identifier.startpage552
dc.identifier.endpage552
dc.identifier.name-orcidRej, Rohan Kalyan; 0000-0003-0904-9137
dc.identifier.name-orcidRoy, Joyeeta
dc.identifier.name-orcidAllu, Srinivasa Rao; 0000-0001-9178-2578
dc.working.doi10.7302/22163en
dc.owningcollnameInternal Medicine, Department of


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