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dc.contributor.authorCheang, MCU
dc.contributor.authorBliss, JM
dc.contributor.authorViale, G
dc.contributor.authorSpeirs, V
dc.contributor.authorPalmieri, C
dc.contributor.authorShaaban, A
dc.contributor.authorLønning, PE
dc.contributor.authorMorden, J
dc.contributor.authorPorta, N
dc.contributor.authorJassem, J
dc.contributor.authorvan De Velde, CJ
dc.contributor.authorRasmussen, BB
dc.contributor.authorVerhoeven, D
dc.contributor.authorBartlett, JMS
dc.contributor.authorCoombes, RC
dc.contributor.authorPathIES Sub-Committee,
dc.date.accessioned2017-11-06T16:10:28Z
dc.date.issued2018-02-01
dc.identifier.citationBreast cancer research and treatment, 2018, 168 (1), pp. 169 - 178
dc.identifier.issn0167-6806
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/902
dc.identifier.eissn1573-7217
dc.identifier.doi10.1007/s10549-017-4543-7
dc.description.abstractBACKGROUND: Intergroup Exemestane Study (IES) was a randomised study that showed a survival benefit of switching adjuvant endocrine therapy after 2-3 years from tamoxifen to exemestane. This PathIES aimed to assess the role of immunohistochemical (IHC)4 score in determining the relative sensitivity to either tamoxifen or sequential treatment with tamoxifen and exemestane. PATIENTS AND METHODS: Primary tumour samples were available for 1274 patients (27% of IES population). Only patients for whom the IHC4 score could be calculated (based on oestrogen receptor, progesterone receptor, HER2 and Ki67) were included in this analysis (N = 430 patients). The clinical score (C) was based on age, grade, tumour size and nodal status. The association of clinicopathological parameters, IHC4(+C) scores and treatment effect with time to distant recurrence-free survival (TTDR) was assessed in univariable and multivariable Cox regression analyses. A modified clinical score (PathIEscore) (N = 350) was also estimated. RESULTS: Our results confirm the prognostic importance of the original IHC4, alone and in conjunction with clinical scores, but no significant difference with treatment effects was observed. The combined IHC4 + Clinical PathIES score was prognostic for TTDR (P < 0.001) with a hazard ratio (HR) of 5.54 (95% CI 1.29-23.70) for a change from 1st quartile (Q1) to Q1-Q3 and HR of 15.54 (95% CI 3.70-65.24) for a change from Q1 to Q4. CONCLUSION: In the PathIES population, the IHC4 score is useful in predicting long-term relapse in patients who remain disease-free after 2-3 years. This is a first trial to suggest the extending use of IHC4+C score for prognostic indication for patients who have switched endocrine therapies at 2-3 years and who remain disease-free after 2-3 years.
dc.formatPrint-Electronic
dc.format.extent169 - 178
dc.languageeng
dc.language.isoeng
dc.publisherSPRINGER
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectPathIES Sub-Committee
dc.subjectBreast
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectNeoplasm Recurrence, Local
dc.subjectTamoxifen
dc.subjectAndrostadienes
dc.subjectReceptors, Estrogen
dc.subjectReceptors, Progesterone
dc.subjectAntineoplastic Agents, Hormonal
dc.subjectPrognosis
dc.subjectDisease-Free Survival
dc.subjectChemotherapy, Adjuvant
dc.subjectMastectomy
dc.subjectImmunohistochemistry
dc.subjectDouble-Blind Method
dc.subjectDrug Resistance, Neoplasm
dc.subjectTime Factors
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.titleEvaluation of applying IHC4 as a prognostic model in the translational study of Intergroup Exemestane Study (IES): PathIES.
dc.typeJournal Article
dcterms.dateAccepted2017-10-16
rioxxterms.funderThe Institute of Cancer Research
rioxxterms.identifier.projectUnspecified
rioxxterms.versionofrecord10.1007/s10549-017-4543-7
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-02
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBreast cancer research and treatment
pubs.issue1
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/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Genomic Analysis – Clinical Trials
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/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Genomic Analysis – Clinical Trials
pubs.publication-statusPublished
pubs.volume168
pubs.embargo.termsNot known
icr.researchteamClinical Trials & Statistics Unit
icr.researchteamGenomic Analysis – Clinical Trials
dc.contributor.icrauthorCheang, Chon
dc.contributor.icrauthorBliss, Judith
dc.contributor.icrauthorPorta, Nuria


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