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dc.contributor.authorHelland, Thomas
dc.contributor.authorNaume, Bjørn
dc.contributor.authorHustad, Steinar
dc.contributor.authorBifulco, Ersilia
dc.contributor.authorKvaløy, Jan Terje
dc.contributor.authorSætersdal, Anna Barbro
dc.contributor.authorSynnestvedt, Marit
dc.contributor.authorLende, Tone Hoel
dc.contributor.authorGilje, Bjørnar
dc.contributor.authorMjaaland, Ingvil
dc.contributor.authorWeyde, Kjetil
dc.contributor.authorBlix, Egil Støre
dc.contributor.authorWiedswang, Gro
dc.contributor.authorBorgen, Elin
dc.contributor.authorHertz, Daniel Louis
dc.contributor.authorJanssen, Emiel
dc.contributor.authorMellgren, Gunnar
dc.contributor.authorSøiland, Håvard
dc.date.accessioned2021-07-07T14:10:37Z
dc.date.available2021-07-07T14:10:37Z
dc.date.created2021-02-16T15:33:38Z
dc.date.issued2021
dc.identifier.issn1574-7891
dc.identifier.urihttps://hdl.handle.net/11250/2763837
dc.description.abstractLow steady‐state levels of active tamoxifen metabolites have been associated with inferior treatment outcomes. In this retrospective analysis of 406 estrogen receptor‐positive breast cancer (BC) patients receiving adjuvant tamoxifen as initial treatment, we have associated our previously reported thresholds for the two active metabolites, Z‐endoxifen and Z‐4‐hydroxy‐tamoxifen (Z‐4OHtam), with treatment outcomes in an independent cohort of BC patients. Among all patients, metabolite levels did not affect survival. However, in the premenopausal subgroup receiving tamoxifen alone (n = 191) we confirmed an inferior BC ‐specific survival in patients with the previously described serum concentration threshold of Z‐4OHtam ≤ 3.26 nm (HR = 2.37, 95% CI = 1.02–5.48, P = 0.039). The ‘dose–response’ survival trend in patients categorized to ordinal concentration cut‐points of Z‐4OHtamoxifen (≤ 3.26, 3.27–8.13, > 8.13 nm) was also replicated (P‐trend log‐rank = 0.048). Z‐endoxifen was not associated with outcome. This is the first study to confirm the association between a published active tamoxifen metabolite threshold and BC outcome in an independent patient cohort. Premenopausal patients receiving 5‐year of tamoxifen alone may benefit from therapeutic drug monitoring to ensure tamoxifen effectiveness.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleLow Z-4OHtam concentrations are associated with adverse clinical outcome among early stage premenopausal breast cancer patients treated with adjuvant tamoxifenen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2020 the authorsen_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1002/1878-0261.12865
dc.identifier.cristin1890507
dc.source.journalMolecular Oncologyen_US
dc.source.pagenumber957-967en_US
dc.identifier.citationMolecular Oncology. 2021, 15 (4), 957-967.en_US
dc.source.volume15en_US
dc.source.issue4en_US


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