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dc.contributor.authorMuller, I
dc.contributor.authorKilburn, LS
dc.contributor.authorTaylor, PN
dc.contributor.authorBarrett-Lee, PJ
dc.contributor.authorBliss, JM
dc.contributor.authorEllis, P
dc.contributor.authorLudgate, ME
dc.contributor.authorDayan, CM
dc.date.accessioned2017-10-05T15:15:09Z
dc.date.accessioned2020-06-22T10:04:21Z
dc.date.issued2017-07-01
dc.identifier.citationEuropean thyroid journal, 2017, 6 (4), pp. 197 - 207
dc.identifier.issn2235-0640
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3760
dc.identifier.eissn2235-0802
dc.identifier.doi10.1159/000460246
dc.description.abstractBACKGROUND: Small-scale studies correlated the presence of thyroid autoimmunity with both improved or worsened breast cancer outcome. OBJECTIVES: We aimed to clarify this association in a large cohort using the phase III, randomized, controlled Taxotere as Adjuvant Chemotherapy Trial (TACT, CRUK01/001). METHODS: TACT women >18 years old with node-positive or high-risk node-negative early breast cancer (pT1-3a, pN0-1, M0), with stored plasma (n = 1,974), taken 15.5 (median; IQR 7.0-24.0) months after breast surgery were studied. Patients had also received chemotherapy (100%), radiotherapy (1,745/1,974; 88.4%), hormonal therapy (1,378/ 1,974; 69.8%), or trastuzumab (48/1,974; 2.4%). History of thyroid diseases and/or related treatments was not available. The prognostic significance of autoantibodies to thyroid peroxidase (TPOAb; positive ≥6 kIU/L), free-thyroxine and thyrotropin (combined: euthyroid, hypothyroid, hyperthyroid) was evaluated for disease-free survival (DFS), overall-survival (OS), and time-to-recurrence (TTR), with Cox regression models in univariate and multivariable analyses. The extended median follow-up was 97.5 months. RESULTS: No difference in DFS was found by TPOAb status (unadjusted hazard ratio [HR]: 0.97, 95%CI: 0.78-1.19; p = 0.75) and/or thyroid function (unadjusted HR [hypothyroid vs. euthyroid]: 1.15, 95% CI: 0.79-1.68; p = 0.46; unadjusted HR [hyperthyroid vs. euthyroid]: 1.14, 95% CI: 0.82-1.61; p = 0.44). Similar results were obtained for OS, TTR, multivariable analyses, when TPOAb titre by tertiles was considered, and in a subgroup of 123 patients with plasma collected before adjuvant treatments. CONCLUSIONS: No evidence for a prognostic role of TPOAb and/or thyroid function in moderate-to-high-risk early breast cancer was found in the largest and longest observational study to date.
dc.formatPrint-Electronic
dc.format.extent197 - 207
dc.languageeng
dc.language.isoeng
dc.publisherKARGER
dc.relation.replaceshttps://repository.icr.ac.uk/handle/internal/848
dc.relation.replacesinternal/848
dc.relation.replacesinternal/820
dc.relation.replaceshttps://repository.icr.ac.uk/handle/internal/820
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved
dc.titleTPOAb and Thyroid Function Are Not Associated with Breast Cancer Outcome: Evidence from a Large-Scale Study Using Data from the Taxotere as Adjuvant Chemotherapy Trial (TACT, CRUK01/001).
dc.typeJournal Article
dcterms.dateAccepted2017-02-07
rioxxterms.funderThe Institute of Cancer Research
rioxxterms.identifier.projectUnspecified
rioxxterms.versionofrecord10.1159/000460246
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean thyroid journal
pubs.issue4
pubs.notesIndefinite
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
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.publication-statusPublished
pubs.volume6
pubs.embargo.termsIndefinite
icr.researchteamClinical Trials & Statistics Unit
dc.contributor.icrauthorKilburn, Lucy
dc.contributor.icrauthorBliss, Judith


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