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Ethnic Diversity of DPD Activity and the DPYD Gene: Review of the Literature
Pharmacogenomic screening can identify patients with gene variants that predispose them to the development of severe toxicity from fluoropyrimidine (FP) chemotherapy. Deficiency of the critical metabolic enzyme dihydropyrimidine dehydrogenase (DPD) leads to excessive toxicity on exposure to fluoropy...
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Published in: | Pharmacogenomics and personalized medicine 2021-01, Vol.14, p.1603-1617 |
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description | Pharmacogenomic screening can identify patients with gene variants that predispose them to the development of severe toxicity from fluoropyrimidine (FP) chemotherapy. Deficiency of the critical metabolic enzyme dihydropyrimidine dehydrogenase (DPD) leads to excessive toxicity on exposure to fluoropyrimidine chemotherapy. This can result in hospitalisation, intensive care admissions and even death. Upfront screening of the gene that encodes for DPD (
) has recently been implemented in regions throughout Europe and the United Kingdom. Current screening evaluates
variants that are well described within Caucasian patient populations and provides genotyped-guided dose adjustment recommendations based upon the presence of these variants. This article reviews the differences in
gene variants within non-Caucasian populations compared to Caucasian populations, with regard to the implications for clinical tolerance of fluoropyrimidine chemotherapies and genotype guided dose adjustment guidelines. |
doi_str_mv | 10.2147/PGPM.S337147 |
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) has recently been implemented in regions throughout Europe and the United Kingdom. Current screening evaluates
variants that are well described within Caucasian patient populations and provides genotyped-guided dose adjustment recommendations based upon the presence of these variants. This article reviews the differences in
gene variants within non-Caucasian populations compared to Caucasian populations, with regard to the implications for clinical tolerance of fluoropyrimidine chemotherapies and genotype guided dose adjustment guidelines.</description><identifier>ISSN: 1178-7066</identifier><identifier>EISSN: 1178-7066</identifier><identifier>DOI: 10.2147/PGPM.S337147</identifier><identifier>PMID: 34916829</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Cancer ; Cancer therapies ; Chemotherapy ; Dehydrogenases ; dihydropyrimidine dehydrogenase ; dpyd gene ; Enzymes ; Genes ; Genotypes ; Investigations ; Literature reviews ; Metabolism ; Metabolites ; Multiculturalism ; Multiculturalism & pluralism ; non-caucasian ; Patients ; Pharmacogenetics ; Pharmacogenomics ; Review ; Toxicity ; White people</subject><ispartof>Pharmacogenomics and personalized medicine, 2021-01, Vol.14, p.1603-1617</ispartof><rights>2021 White et al.</rights><rights>COPYRIGHT 2021 Dove Medical Press Limited</rights><rights>2021. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 White et al. 2021 White et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c576t-9ccb0dd622f3a6fb3495333220c5eacf8cdee08b3dcb8fa2942c4c4de5b45ec3</citedby><cites>FETCH-LOGICAL-c576t-9ccb0dd622f3a6fb3495333220c5eacf8cdee08b3dcb8fa2942c4c4de5b45ec3</cites><orcidid>0000-0001-5268-2793</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2611006330/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2611006330?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34916829$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>White, Cassandra</creatorcontrib><creatorcontrib>Scott, Rodney J</creatorcontrib><creatorcontrib>Paul, Christine</creatorcontrib><creatorcontrib>Ziolkowski, Andrew</creatorcontrib><creatorcontrib>Mossman, David</creatorcontrib><creatorcontrib>Ackland, Stephen</creatorcontrib><title>Ethnic Diversity of DPD Activity and the DPYD Gene: Review of the Literature</title><title>Pharmacogenomics and personalized medicine</title><addtitle>Pharmgenomics Pers Med</addtitle><description>Pharmacogenomic screening can identify patients with gene variants that predispose them to the development of severe toxicity from fluoropyrimidine (FP) chemotherapy. Deficiency of the critical metabolic enzyme dihydropyrimidine dehydrogenase (DPD) leads to excessive toxicity on exposure to fluoropyrimidine chemotherapy. This can result in hospitalisation, intensive care admissions and even death. Upfront screening of the gene that encodes for DPD (
) has recently been implemented in regions throughout Europe and the United Kingdom. Current screening evaluates
variants that are well described within Caucasian patient populations and provides genotyped-guided dose adjustment recommendations based upon the presence of these variants. This article reviews the differences in
gene variants within non-Caucasian populations compared to Caucasian populations, with regard to the implications for clinical tolerance of fluoropyrimidine chemotherapies and genotype guided dose adjustment guidelines.</description><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Dehydrogenases</subject><subject>dihydropyrimidine dehydrogenase</subject><subject>dpyd gene</subject><subject>Enzymes</subject><subject>Genes</subject><subject>Genotypes</subject><subject>Investigations</subject><subject>Literature reviews</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Multiculturalism</subject><subject>Multiculturalism & pluralism</subject><subject>non-caucasian</subject><subject>Patients</subject><subject>Pharmacogenetics</subject><subject>Pharmacogenomics</subject><subject>Review</subject><subject>Toxicity</subject><subject>White people</subject><issn>1178-7066</issn><issn>1178-7066</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk2P0zAQhiMEYpeFG2cUCQlxoMUfsZNwQKq2S1mpiAr2wslynHHjKrUX2ynaf4-zLUuLkA_2zDzzejyeLHuJ0ZTgony_Wqy-TL9TWibjUXaOcVlNSsT546PzWfYshA1Kp4qSp9kZLWrMK1KfZ8ur2Fmj8rnZgQ8m3uVO5_PVPJ-paHajLW2bxw6S88c8X4CFD_k32Bn4NZJjYGkieBkHD8-zJ1r2AV4c9ovs5tPVzeXnyfLr4vpytpwoVvI4qZVqUNtyQjSVXDepGkYpJQQpBlLpSrUAqGpoq5pKS1IXRBWqaIE1BQNFL7LrvWzr5EbcerOV_k44acS9w_m1kD4a1YNgmNNSIl42mheUogZkwSWrSINYXSCWtD7utW6HZgutAhu97E9ETyPWdGLtdqJKvSSsTAJvDwLe_RwgRLE1QUHfSwtuCIJwjDmrClwn9PU_6MYN3qZO3VPpe1KFf6m1TA8wVrt0rxpFxYxXNUvFI5qo6X-otFrYGuUsaJP8JwlvjhI6kH3sguuHaJwNp-C7Pai8C8GDfmgGRmKcODFOnDhMXMJfHTfwAf4zYvQ3AIrNXQ</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>White, Cassandra</creator><creator>Scott, Rodney J</creator><creator>Paul, Christine</creator><creator>Ziolkowski, Andrew</creator><creator>Mossman, David</creator><creator>Ackland, Stephen</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>KB0</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5268-2793</orcidid></search><sort><creationdate>20210101</creationdate><title>Ethnic Diversity of DPD Activity and the DPYD Gene: Review of the Literature</title><author>White, Cassandra ; 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Deficiency of the critical metabolic enzyme dihydropyrimidine dehydrogenase (DPD) leads to excessive toxicity on exposure to fluoropyrimidine chemotherapy. This can result in hospitalisation, intensive care admissions and even death. Upfront screening of the gene that encodes for DPD (
) has recently been implemented in regions throughout Europe and the United Kingdom. Current screening evaluates
variants that are well described within Caucasian patient populations and provides genotyped-guided dose adjustment recommendations based upon the presence of these variants. This article reviews the differences in
gene variants within non-Caucasian populations compared to Caucasian populations, with regard to the implications for clinical tolerance of fluoropyrimidine chemotherapies and genotype guided dose adjustment guidelines.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>34916829</pmid><doi>10.2147/PGPM.S337147</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-5268-2793</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cancer Cancer therapies Chemotherapy Dehydrogenases dihydropyrimidine dehydrogenase dpyd gene Enzymes Genes Genotypes Investigations Literature reviews Metabolism Metabolites Multiculturalism Multiculturalism & pluralism non-caucasian Patients Pharmacogenetics Pharmacogenomics Review Toxicity White people |
title | Ethnic Diversity of DPD Activity and the DPYD Gene: Review of the Literature |
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