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dc.contributor.authorRichman, J
dc.contributor.authorRing, A
dc.contributor.authorDowsett, M
dc.contributor.authorSestak, I
dc.coverage.spatialNetherlands
dc.date.accessioned2022-09-02T08:16:13Z
dc.date.available2022-09-02T08:16:13Z
dc.date.issued2020-11-21
dc.identifier10.1007/s10549-020-06013-6
dc.identifier.citationBreast Cancer Research and Treatment, 2020, 186 (1), pp. 115 - 123en_US
dc.identifier.issn0167-6806
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5374
dc.identifier.eissn1573-7217
dc.identifier.eissn1573-7217
dc.identifier.doi10.1007/s10549-020-06013-6
dc.description.abstractPURPOSE: Clinical Treatment Score at 5 years (CTS5) is a prognostic tool to estimate distant recurrence (DR) risk after 5 years of endocrine therapy for postmenopausal women with oestrogen receptor-positive (ER-positive) breast cancer. METHODS: The validity of CTS5 was tested in a retrospective cohort of patients diagnosed with early ER-positive breast cancer. The primary endpoint was DR in years 5-10. The primary analysis cohort consisted of postmenopausal women, with premenopausal women as a secondary analysis cohort. Cox regression models were used to determine the prognostic value of CTS5 and Kaplan-Meier curves were used with associated 10-year DR risks (%). RESULTS: 2428 women were included with a median follow-up of 13.4 years. The CTS5 was significantly prognostic in both postmenopausal (N = 1662, HR = 2.18 95% CI (1.78-2.67)) and premenopausal women (N = 766, HR = 1.84 95% CI (1.32-2.56)). The 10-year DR risks were 2.9% (1.9-4.5), 7.2% (5.3-9.9), and 12.9% (10.0-16.7) for low, intermediate and high risk in postmenopausal women and 3.8% (2.2-6.7), 6.9% (4.4-10.8), and 11.1% (7.4-16.5) in premenopausal women, respectively. The number of observed DRs was significantly greater than expected in those predicted to be at high risk by CTS5 but this discordance was lost when those receiving more than 60 months of endocrine therapy were excluded. CONCLUSIONS: The CTS5 demonstrated clinical validity for predicting late DR within a large cohort of unselected postmenopausal patients but less so in premenopausal patients. Calibration of the CTS5 was good in patients who did not receive extended endocrine therapy. The CTS5 low-risk cohort has risk of DR so low as to not warrant extended endocrine therapy.
dc.formatPrint-Electronic
dc.format.extent115 - 123
dc.languageeng
dc.language.isoengen_US
dc.publisherSPRINGERen_US
dc.relation.ispartofBreast Cancer Research and Treatment
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectBreast cancer
dc.subjectExtended endocrine therapy
dc.subjectLate metastasis
dc.subjectPrediction
dc.subjectAntineoplastic Agents, Hormonal
dc.subjectBreast Neoplasms
dc.subjectFemale
dc.subjectHumans
dc.subjectNeoplasm Recurrence, Local
dc.subjectPrognosis
dc.subjectReceptors, Estrogen
dc.subjectRetrospective Studies
dc.subjectTamoxifen
dc.titleClinical validity of clinical treatment score 5 (CTS5) for estimating risk of late recurrence in unselected, non-trial patients with early oestrogen receptor-positive breast cancer.en_US
dc.typeJournal Article
dcterms.dateAccepted2020-11-03
dc.date.updated2022-09-02T08:15:48Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1007/s10549-020-06013-6en_US
rioxxterms.licenseref.startdate2020-11-21
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33222093
pubs.issue1
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/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Endocrinology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Endocrinology/Endocrinology (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Endocrinology
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1007/s10549-020-06013-6
pubs.volume186
icr.researchteamEndocrinologyen_US
dc.contributor.icrauthorDowsett, Mitch
icr.provenanceDeposited by Mr Arek Surman on 2022-09-02. Deposit type is initial. No. of files: 1. Files: Clinical validity of clinical treatment score 5 (CTS5) for estimating risk of late recurrence in unselected, non-trial patie.pdf


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