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Pharmacogenomics, CYP2D6, and tamoxifen: a survey of the reasons sustaining European clinical practice paradigms

dc.contributor.authorReis, Sara S.
dc.contributor.authorCarvalho, Ana S.
dc.contributor.authorFernandes, Rúben
dc.date.accessioned2019-10-23T10:46:21Z
dc.date.available2019-10-23T10:46:21Z
dc.date.issued2019
dc.description.abstractTamoxifen is a drug that is often used in the clinical management of breast cancer. CYP2D6 is a key metabolizing enzyme that is involved in the conversion of tamoxifen to its active drug metabolites. CYP2D6 has several alleles that metabolize tamoxifen and other drugs at different rates that can alter therapeutic impact, a characteristic that renders it one of the most studied enzymes in the field of pharmacogenetics. Background and objectives: Portugal has no implemented measures based on pharmacogenomics analysis prior to therapy that might function as a cultural sample control when analyzing the individual and economic factors present in clinical practice paradigms. Therefore, we aim to investigate the impact of CYP2D6 genotyping of the tamoxifen metabolizing enzymes in the clinical management of breast cancer patients. Materials and Methods: Qualitative/quantitative studies regarding the impact of pharmacogenomics in breast cancer; personal interviews in different Portuguese laboratories within hospital setting using a survey. Analysis of data through interviews to management board and/or decision makers from major oncological centers. Results: Reasons for common adoption of pharmacogenomics practice are contradictory and based both in economic factors and cultural/clinical bias. Conclusions: This research study identifies specific cultural and/or clinical bias that act as obstacles to pharmacogenomic implementation and proposes viable courses of action that might bring about change in cultural/medical habits.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationReis, Carvalho, & Fernandes. (2019). Pharmacogenomics, CYP2D6, and Tamoxifen: A Survey of the Reasons Sustaining European Clinical Practice Paradigms. Medicina, 55(7), 344. https://doi.org/10.3390/medicina55070344pt_PT
dc.identifier.doi10.3390/medicina55070344pt_PT
dc.identifier.eid85069289922
dc.identifier.eissn1648-9144
dc.identifier.issn1010-660X
dc.identifier.pmcPMC6681270
dc.identifier.pmid31284530
dc.identifier.urihttp://hdl.handle.net/10400.14/28497
dc.identifier.wos000480658200031
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationUID/EQU/0470/2019
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectPharmacogenomicspt_PT
dc.subjectClinical policiespt_PT
dc.subjectClinical biaspt_PT
dc.subjectBreast cancerpt_PT
dc.subjectTamoxifenpt_PT
dc.subjectCYP2D6pt_PT
dc.subjectHormone therapypt_PT
dc.subjectCultural sample controlpt_PT
dc.titlePharmacogenomics, CYP2D6, and tamoxifen: a survey of the reasons sustaining European clinical practice paradigmspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FBIM%2F04293%2F2013/PT
oaire.citation.issue7
oaire.citation.titleMedicinapt_PT
oaire.citation.volume55
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublicationbc5f2a05-bfc8-4ecb-aaed-8a34f487ae13
relation.isProjectOfPublication.latestForDiscoverybc5f2a05-bfc8-4ecb-aaed-8a34f487ae13

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