Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136228
Full metadata record
DC FieldValueLanguage
dc.creatorReis, SS
dc.creatorCarvalho, AS
dc.creatorFernandes, R
dc.date.accessioned2021-09-20T10:52:07Z-
dc.date.available2021-09-20T10:52:07Z-
dc.date.issued2019
dc.identifier.issn1010-660X
dc.identifier.urihttps://hdl.handle.net/10216/136228-
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.
dc.description.sponsorshipThis research was partially support by UID/BIM/04293/2013 and UID/EQU/0470/2019.
dc.language.isoeng
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147342/PT
dc.relation.ispartofMedicina (Lithuania), vol.55(7):344
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBreast cancer
dc.subjectClinical bias
dc.subjectClinical policies
dc.subjectCultural sample control
dc.subjectCYP2D6
dc.subjectHormone therapy
dc.subjectPharmacogenomics
dc.subjectTamoxifen
dc.subject.meshAdult
dc.subject.meshBreast Neoplasms / drug therapy
dc.subject.meshBreast Neoplasms / genetics
dc.subject.meshCytochrome P-450 CYP2D6 / analysis
dc.subject.meshCytochrome P-450 CYP2D6 / genetics
dc.subject.meshExpert Testimony
dc.subject.meshFemale
dc.subject.meshGuidelines as Topic / standards
dc.subject.meshHumans
dc.subject.meshPharmacogenetics / methods
dc.subject.meshPharmacogenetics / standards
dc.subject.meshPortugal
dc.subject.meshSensitivity and Specificity
dc.subject.meshSurveys and Questionnaires
dc.subject.meshTamoxifen / standards
dc.subject.meshTamoxifen / therapeutic use
dc.titlePharmacogenomics, CYP2D6, and tamoxifen: A survey of the reasons sustaining european clinical practice paradigms
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/medicina55070344
dc.relation.publisherversionhttps://www.mdpi.com/1648-9144/55/7/344
Appears in Collections:I3S - Artigo em Revista Científica Internacional

Files in This Item:
File Description SizeFormat 
10.3390-medicina55070344.pdf1.25 MBAdobe PDFThumbnail
View/Open


This item is licensed under a Creative Commons License Creative Commons