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https://hdl.handle.net/10216/136228Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.creator | Reis, SS | |
| dc.creator | Carvalho, AS | |
| dc.creator | Fernandes, R | |
| dc.date.accessioned | 2021-09-20T10:52:07Z | - |
| dc.date.available | 2021-09-20T10:52:07Z | - |
| dc.date.issued | 2019 | |
| dc.identifier.issn | 1010-660X | |
| dc.identifier.uri | https://hdl.handle.net/10216/136228 | - |
| dc.description.abstract | Tamoxifen 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.sponsorship | This research was partially support by UID/BIM/04293/2013 and UID/EQU/0470/2019. | |
| dc.language.iso | eng | |
| dc.publisher | MDPI | |
| dc.relation | info:eu-repo/grantAgreement/FCT/5876/147342/PT | |
| dc.relation.ispartof | Medicina (Lithuania), vol.55(7):344 | |
| dc.rights | openAccess | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Breast cancer | |
| dc.subject | Clinical bias | |
| dc.subject | Clinical policies | |
| dc.subject | Cultural sample control | |
| dc.subject | CYP2D6 | |
| dc.subject | Hormone therapy | |
| dc.subject | Pharmacogenomics | |
| dc.subject | Tamoxifen | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Breast Neoplasms / drug therapy | |
| dc.subject.mesh | Breast Neoplasms / genetics | |
| dc.subject.mesh | Cytochrome P-450 CYP2D6 / analysis | |
| dc.subject.mesh | Cytochrome P-450 CYP2D6 / genetics | |
| dc.subject.mesh | Expert Testimony | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Guidelines as Topic / standards | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Pharmacogenetics / methods | |
| dc.subject.mesh | Pharmacogenetics / standards | |
| dc.subject.mesh | Portugal | |
| dc.subject.mesh | Sensitivity and Specificity | |
| dc.subject.mesh | Surveys and Questionnaires | |
| dc.subject.mesh | Tamoxifen / standards | |
| dc.subject.mesh | Tamoxifen / therapeutic use | |
| dc.title | Pharmacogenomics, CYP2D6, and tamoxifen: A survey of the reasons sustaining european clinical practice paradigms | |
| dc.type | Artigo em Revista Científica Internacional | |
| dc.contributor.uporto | Instituto de Investigação e Inovação em Saúde | |
| dc.identifier.doi | 10.3390/medicina55070344 | |
| dc.relation.publisherversion | https://www.mdpi.com/1648-9144/55/7/344 | |
| Appears in Collections: | I3S - Artigo em Revista Científica Internacional | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 10.3390-medicina55070344.pdf | 1.25 MB | Adobe PDF | ![]() View/Open |
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