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dc.contributor.authorTurner, NC
dc.contributor.authorNeven, P
dc.contributor.authorLoibl, S
dc.contributor.authorAndre, F
dc.date.accessioned2017-11-24T11:44:42Z
dc.date.accessioned2017-11-24T11:49:03Z
dc.date.issued2017-06-17
dc.identifier.citationLancet (London, England), 2017, 389 (10087), pp. 2403 - 2414
dc.identifier.issn0140-6736
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/949
dc.identifier.eissn1474-547X
dc.identifier.doi10.1016/s0140-6736(16)32419-9
dc.description.abstractOestrogen-receptor-positive breast cancer is the most common subtype of breast cancer. Endocrine therapies that target the dependence of this subtype on the oestrogen receptor have substantial activity, yet the development of resistance to therapy is inevitable in advanced cancer. Major progress has been made in identifying the drivers of oestrogen-receptor-positive breast cancer and the mechanisms of resistance to endocrine therapy. This progress has translated into major advances in the treatment of advanced breast cancer, with several targeted therapies that enhance the efficacy of endocrine therapy; inhibitors of mTOR and inhibitors of the cyclin-dependent kinases CDK4 and CDK6 substantially improve progression-free survival. A new wave of targeted therapies is being developed, including inhibitors of PI3K, AKT, and HER2, and a new generation of oestrogen-receptor degraders. Considerable challenges remain in patient selection, deciding on the most appropriate order in which to administer therapies, and establishing whether cross-resistance occurs between therapies.
dc.formatPrint-Electronic
dc.format.extent2403 - 2414
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCIENCE INC
dc.relation.replaceshttps://repository.icr.ac.uk/handle/internal/948
dc.relation.replacesinternal/948
dc.rights.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectPiperazines
dc.subjectPyridines
dc.subjectNuclear Proteins
dc.subjectReceptors, Estrogen
dc.subjectTranscription Factors
dc.subjectAntineoplastic Agents
dc.subjectAromatase Inhibitors
dc.subjectFemale
dc.subjectCyclin-Dependent Kinase 4
dc.subjectCyclin-Dependent Kinase 6
dc.subjectTOR Serine-Threonine Kinases
dc.subjectMolecular Targeted Therapy
dc.titleAdvances in the treatment of advanced oestrogen-receptor-positive breast cancer.
dc.typeJournal Article
dcterms.dateAccepted2016-08-24
rioxxterms.versionofrecord10.1016/s0140-6736(16)32419-9
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
rioxxterms.licenseref.startdate2017-06
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfLancet (London, England)
pubs.issue10087
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume389
pubs.embargo.termsNot known
icr.researchteamMolecular Oncology
dc.contributor.icrauthorTurner, Nicholas


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