Loading…
Evaluation of clinical implementation of prospective
Fluoropyrimidines are commonly used anti-cancer drugs, but lead to severe toxicity in 10-30% of patients. Prospective screening identifies patients at risk for toxicity and leads to a safer treatment with fluoropyrimidines. This study evaluated the routinely application of prospective screening at t...
Saved in:
Published in: | Pharmacogenomics 2016-05, Vol.17 (7), p.721-729 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 729 |
container_issue | 7 |
container_start_page | 721 |
container_title | Pharmacogenomics |
container_volume | 17 |
creator | Lunenburg, Carin ATC van Staveren, Maurice C Gelderblom, Hans Guchelaar, Henk-Jan Swen, Jesse J |
description | Fluoropyrimidines are commonly used anti-cancer drugs, but lead to severe toxicity in 10-30% of patients. Prospective
screening identifies patients at risk for toxicity and leads to a safer treatment with fluoropyrimidines. This study evaluated the routinely application of prospective
screening at the Leiden University Medical Center.
Prospective
screening as part of routine patient care was evaluated by retrospectively screening databases and patient files to determine genotype, treatment, dose recommendations and dose adjustments.
86.9% of all patients with a first fluoropyrimidine prescription were screened. Fourteen out of 275 patients (5.1%) carried a
variant and received a 25-50% dose reduction recommendation. None of the patients with a
variant treated with a reduced dose developed toxicities.
Prospective
screening can be implemented successfully in a real world clinical setting, is well accepted by physicians and results in low toxicity. |
doi_str_mv | 10.2217/pgs-2016-0013 |
format | article |
fullrecord | <record><control><sourceid>futurescience</sourceid><recordid>TN_cdi_futurescience_futuremedicine_10_2217_pgs_2016_0013</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_2217_pgs_2016_0013</sourcerecordid><originalsourceid>FETCH-futurescience_futuremedicine_10_2217_pgs_2016_00133</originalsourceid><addsrcrecordid>eNqlzk0KwjAQBeAgCv4u3fcC0Zk0pLqWigdwH0qcSiRNQ5P2_LYoXsDVvOHx4GNsj3AQAotjeEYuABUHwHzGVlhIyU8gxXzMUgkuJKolW8f4AhCoJKyYLIfK9VWyrc_aOjPOemsql9kmOGrIp18VujYGMskOtGWLunKRdt-7Yedreb_ceN2nvqNoLHlD-vM19LDGetIIemLqkaknpp6Y-T_bNzgLSx8</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Evaluation of clinical implementation of prospective</title><source>PubMed Central(OpenAccess)</source><creator>Lunenburg, Carin ATC ; van Staveren, Maurice C ; Gelderblom, Hans ; Guchelaar, Henk-Jan ; Swen, Jesse J</creator><creatorcontrib>Lunenburg, Carin ATC ; van Staveren, Maurice C ; Gelderblom, Hans ; Guchelaar, Henk-Jan ; Swen, Jesse J</creatorcontrib><description>Fluoropyrimidines are commonly used anti-cancer drugs, but lead to severe toxicity in 10-30% of patients. Prospective
screening identifies patients at risk for toxicity and leads to a safer treatment with fluoropyrimidines. This study evaluated the routinely application of prospective
screening at the Leiden University Medical Center.
Prospective
screening as part of routine patient care was evaluated by retrospectively screening databases and patient files to determine genotype, treatment, dose recommendations and dose adjustments.
86.9% of all patients with a first fluoropyrimidine prescription were screened. Fourteen out of 275 patients (5.1%) carried a
variant and received a 25-50% dose reduction recommendation. None of the patients with a
variant treated with a reduced dose developed toxicities.
Prospective
screening can be implemented successfully in a real world clinical setting, is well accepted by physicians and results in low toxicity.</description><identifier>ISSN: 1462-2416</identifier><identifier>EISSN: 1744-8042</identifier><identifier>DOI: 10.2217/pgs-2016-0013</identifier><language>eng</language><publisher>Future Medicine Ltd</publisher><subject>5-fluorouracil ; capecitabine ; dihydropyrimidine dehydrogenase ; dose reductions ; fluoropyrimidines ; implementation ; screening</subject><ispartof>Pharmacogenomics, 2016-05, Vol.17 (7), p.721-729</ispartof><rights>Future Medicine Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Lunenburg, Carin ATC</creatorcontrib><creatorcontrib>van Staveren, Maurice C</creatorcontrib><creatorcontrib>Gelderblom, Hans</creatorcontrib><creatorcontrib>Guchelaar, Henk-Jan</creatorcontrib><creatorcontrib>Swen, Jesse J</creatorcontrib><title>Evaluation of clinical implementation of prospective</title><title>Pharmacogenomics</title><description>Fluoropyrimidines are commonly used anti-cancer drugs, but lead to severe toxicity in 10-30% of patients. Prospective
screening identifies patients at risk for toxicity and leads to a safer treatment with fluoropyrimidines. This study evaluated the routinely application of prospective
screening at the Leiden University Medical Center.
Prospective
screening as part of routine patient care was evaluated by retrospectively screening databases and patient files to determine genotype, treatment, dose recommendations and dose adjustments.
86.9% of all patients with a first fluoropyrimidine prescription were screened. Fourteen out of 275 patients (5.1%) carried a
variant and received a 25-50% dose reduction recommendation. None of the patients with a
variant treated with a reduced dose developed toxicities.
Prospective
screening can be implemented successfully in a real world clinical setting, is well accepted by physicians and results in low toxicity.</description><subject>5-fluorouracil</subject><subject>capecitabine</subject><subject>dihydropyrimidine dehydrogenase</subject><subject>dose reductions</subject><subject>fluoropyrimidines</subject><subject>implementation</subject><subject>screening</subject><issn>1462-2416</issn><issn>1744-8042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqlzk0KwjAQBeAgCv4u3fcC0Zk0pLqWigdwH0qcSiRNQ5P2_LYoXsDVvOHx4GNsj3AQAotjeEYuABUHwHzGVlhIyU8gxXzMUgkuJKolW8f4AhCoJKyYLIfK9VWyrc_aOjPOemsql9kmOGrIp18VujYGMskOtGWLunKRdt-7Yedreb_ceN2nvqNoLHlD-vM19LDGetIIemLqkaknpp6Y-T_bNzgLSx8</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Lunenburg, Carin ATC</creator><creator>van Staveren, Maurice C</creator><creator>Gelderblom, Hans</creator><creator>Guchelaar, Henk-Jan</creator><creator>Swen, Jesse J</creator><general>Future Medicine Ltd</general><scope/></search><sort><creationdate>20160501</creationdate><title>Evaluation of clinical implementation of prospective</title><author>Lunenburg, Carin ATC ; van Staveren, Maurice C ; Gelderblom, Hans ; Guchelaar, Henk-Jan ; Swen, Jesse J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-futurescience_futuremedicine_10_2217_pgs_2016_00133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>5-fluorouracil</topic><topic>capecitabine</topic><topic>dihydropyrimidine dehydrogenase</topic><topic>dose reductions</topic><topic>fluoropyrimidines</topic><topic>implementation</topic><topic>screening</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lunenburg, Carin ATC</creatorcontrib><creatorcontrib>van Staveren, Maurice C</creatorcontrib><creatorcontrib>Gelderblom, Hans</creatorcontrib><creatorcontrib>Guchelaar, Henk-Jan</creatorcontrib><creatorcontrib>Swen, Jesse J</creatorcontrib><jtitle>Pharmacogenomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lunenburg, Carin ATC</au><au>van Staveren, Maurice C</au><au>Gelderblom, Hans</au><au>Guchelaar, Henk-Jan</au><au>Swen, Jesse J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of clinical implementation of prospective</atitle><jtitle>Pharmacogenomics</jtitle><date>2016-05-01</date><risdate>2016</risdate><volume>17</volume><issue>7</issue><spage>721</spage><epage>729</epage><pages>721-729</pages><issn>1462-2416</issn><eissn>1744-8042</eissn><abstract>Fluoropyrimidines are commonly used anti-cancer drugs, but lead to severe toxicity in 10-30% of patients. Prospective
screening identifies patients at risk for toxicity and leads to a safer treatment with fluoropyrimidines. This study evaluated the routinely application of prospective
screening at the Leiden University Medical Center.
Prospective
screening as part of routine patient care was evaluated by retrospectively screening databases and patient files to determine genotype, treatment, dose recommendations and dose adjustments.
86.9% of all patients with a first fluoropyrimidine prescription were screened. Fourteen out of 275 patients (5.1%) carried a
variant and received a 25-50% dose reduction recommendation. None of the patients with a
variant treated with a reduced dose developed toxicities.
Prospective
screening can be implemented successfully in a real world clinical setting, is well accepted by physicians and results in low toxicity.</abstract><pub>Future Medicine Ltd</pub><doi>10.2217/pgs-2016-0013</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1462-2416 |
ispartof | Pharmacogenomics, 2016-05, Vol.17 (7), p.721-729 |
issn | 1462-2416 1744-8042 |
language | eng |
recordid | cdi_futurescience_futuremedicine_10_2217_pgs_2016_0013 |
source | PubMed Central(OpenAccess) |
subjects | 5-fluorouracil capecitabine dihydropyrimidine dehydrogenase dose reductions fluoropyrimidines implementation screening |
title | Evaluation of clinical implementation of prospective |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T13%3A11%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-futurescience&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evaluation%20of%20clinical%20implementation%20of%20prospective&rft.jtitle=Pharmacogenomics&rft.au=Lunenburg,%20Carin%20ATC&rft.date=2016-05-01&rft.volume=17&rft.issue=7&rft.spage=721&rft.epage=729&rft.pages=721-729&rft.issn=1462-2416&rft.eissn=1744-8042&rft_id=info:doi/10.2217/pgs-2016-0013&rft_dat=%3Cfuturescience%3E10_2217_pgs_2016_0013%3C/futurescience%3E%3Cgrp_id%3Ecdi_FETCH-futurescience_futuremedicine_10_2217_pgs_2016_00133%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |