Loading…
Polymorphisms in
Sorafenib-treated patients display a substantial variation in the incidence of toxicity. We aimed to investigate the association of genetic polymorphisms with observed toxicity on sorafenib. We genotyped 114 patients that were treated with sorafenib at the Erasmus MC Cancer Institute, the Netherland...
Saved in:
Published in: | Pharmacogenomics 2016-09, Vol.17 (14), p.1483-1490 |
---|---|
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 | 1490 |
container_issue | 14 |
container_start_page | 1483 |
container_title | Pharmacogenomics |
container_volume | 17 |
creator | Bins, Sander Lenting, Anne El Bouazzaoui, Samira van Doorn, Leni Oomen-de Hoop, Esther Eskens, Ferry ALM van Schaik, Ron HN Mathijssen, Ron HJ |
description | Sorafenib-treated patients display a substantial variation in the incidence of toxicity. We aimed to investigate the association of genetic polymorphisms with observed toxicity on sorafenib.
We genotyped 114 patients that were treated with sorafenib at the Erasmus MC Cancer Institute, the Netherlands, for
and
.
The
(rs8175347) polymorphism was associated with hyperbilirubinemia and treatment interruption. Polymorphisms in
(rs2306283, rs4149056) were associated with diarrhea and thrombocytopenia, respectively. None of the investigated polymorphisms was associated with overall or progression-free survival in hepatocellular cancer patients.
Polymorphisms in
and
are associated with several different sorafenib side effects. |
doi_str_mv | 10.2217/pgs-2016-0063 |
format | article |
fullrecord | <record><control><sourceid>futurescience</sourceid><recordid>TN_cdi_futurescience_futuremedicine_10_2217_pgs_2016_0063</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_2217_pgs_2016_0063</sourcerecordid><originalsourceid>FETCH-futurescience_futuremedicine_10_2217_pgs_2016_00633</originalsourceid><addsrcrecordid>eNpjYBA1NNAzMjI01y9IL9Y1MjA00zUwMDNmYuA0NDcx0bUwMDFiAbJNzIx0jUwMzTgYuIqLswwMjAzNTAw4GQQC8nMqc_OLCjIyi3OLFTLzeBhY0xJzilN5oTQ3g6Wba4izh25aaUlpUWpxcmZqXnJqPISXm5qSmZyZlxpvaBAPckI80AnxICfEg5xgTIleAGR7PUw</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Polymorphisms in</title><source>PubMed</source><creator>Bins, Sander ; Lenting, Anne ; El Bouazzaoui, Samira ; van Doorn, Leni ; Oomen-de Hoop, Esther ; Eskens, Ferry ALM ; van Schaik, Ron HN ; Mathijssen, Ron HJ</creator><creatorcontrib>Bins, Sander ; Lenting, Anne ; El Bouazzaoui, Samira ; van Doorn, Leni ; Oomen-de Hoop, Esther ; Eskens, Ferry ALM ; van Schaik, Ron HN ; Mathijssen, Ron HJ</creatorcontrib><description>Sorafenib-treated patients display a substantial variation in the incidence of toxicity. We aimed to investigate the association of genetic polymorphisms with observed toxicity on sorafenib.
We genotyped 114 patients that were treated with sorafenib at the Erasmus MC Cancer Institute, the Netherlands, for
and
.
The
(rs8175347) polymorphism was associated with hyperbilirubinemia and treatment interruption. Polymorphisms in
(rs2306283, rs4149056) were associated with diarrhea and thrombocytopenia, respectively. None of the investigated polymorphisms was associated with overall or progression-free survival in hepatocellular cancer patients.
Polymorphisms in
and
are associated with several different sorafenib side effects.</description><identifier>ISSN: 1462-2416</identifier><identifier>EISSN: 1744-8042</identifier><identifier>DOI: 10.2217/pgs-2016-0063</identifier><language>eng</language><publisher>Future Medicine Ltd</publisher><subject>drug transporters ; hepatocellular carcinoma ; pharmacogenetics ; renal cell cancer ; sorafenib ; toxicity</subject><ispartof>Pharmacogenomics, 2016-09, Vol.17 (14), p.1483-1490</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>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Bins, Sander</creatorcontrib><creatorcontrib>Lenting, Anne</creatorcontrib><creatorcontrib>El Bouazzaoui, Samira</creatorcontrib><creatorcontrib>van Doorn, Leni</creatorcontrib><creatorcontrib>Oomen-de Hoop, Esther</creatorcontrib><creatorcontrib>Eskens, Ferry ALM</creatorcontrib><creatorcontrib>van Schaik, Ron HN</creatorcontrib><creatorcontrib>Mathijssen, Ron HJ</creatorcontrib><title>Polymorphisms in</title><title>Pharmacogenomics</title><description>Sorafenib-treated patients display a substantial variation in the incidence of toxicity. We aimed to investigate the association of genetic polymorphisms with observed toxicity on sorafenib.
We genotyped 114 patients that were treated with sorafenib at the Erasmus MC Cancer Institute, the Netherlands, for
and
.
The
(rs8175347) polymorphism was associated with hyperbilirubinemia and treatment interruption. Polymorphisms in
(rs2306283, rs4149056) were associated with diarrhea and thrombocytopenia, respectively. None of the investigated polymorphisms was associated with overall or progression-free survival in hepatocellular cancer patients.
Polymorphisms in
and
are associated with several different sorafenib side effects.</description><subject>drug transporters</subject><subject>hepatocellular carcinoma</subject><subject>pharmacogenetics</subject><subject>renal cell cancer</subject><subject>sorafenib</subject><subject>toxicity</subject><issn>1462-2416</issn><issn>1744-8042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBA1NNAzMjI01y9IL9Y1MjA00zUwMDNmYuA0NDcx0bUwMDFiAbJNzIx0jUwMzTgYuIqLswwMjAzNTAw4GQQC8nMqc_OLCjIyi3OLFTLzeBhY0xJzilN5oTQ3g6Wba4izh25aaUlpUWpxcmZqXnJqPISXm5qSmZyZlxpvaBAPckI80AnxICfEg5xgTIleAGR7PUw</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Bins, Sander</creator><creator>Lenting, Anne</creator><creator>El Bouazzaoui, Samira</creator><creator>van Doorn, Leni</creator><creator>Oomen-de Hoop, Esther</creator><creator>Eskens, Ferry ALM</creator><creator>van Schaik, Ron HN</creator><creator>Mathijssen, Ron HJ</creator><general>Future Medicine Ltd</general><scope/></search><sort><creationdate>20160901</creationdate><title>Polymorphisms in</title><author>Bins, Sander ; Lenting, Anne ; El Bouazzaoui, Samira ; van Doorn, Leni ; Oomen-de Hoop, Esther ; Eskens, Ferry ALM ; van Schaik, Ron HN ; Mathijssen, Ron HJ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-futurescience_futuremedicine_10_2217_pgs_2016_00633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>drug transporters</topic><topic>hepatocellular carcinoma</topic><topic>pharmacogenetics</topic><topic>renal cell cancer</topic><topic>sorafenib</topic><topic>toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bins, Sander</creatorcontrib><creatorcontrib>Lenting, Anne</creatorcontrib><creatorcontrib>El Bouazzaoui, Samira</creatorcontrib><creatorcontrib>van Doorn, Leni</creatorcontrib><creatorcontrib>Oomen-de Hoop, Esther</creatorcontrib><creatorcontrib>Eskens, Ferry ALM</creatorcontrib><creatorcontrib>van Schaik, Ron HN</creatorcontrib><creatorcontrib>Mathijssen, Ron HJ</creatorcontrib><jtitle>Pharmacogenomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bins, Sander</au><au>Lenting, Anne</au><au>El Bouazzaoui, Samira</au><au>van Doorn, Leni</au><au>Oomen-de Hoop, Esther</au><au>Eskens, Ferry ALM</au><au>van Schaik, Ron HN</au><au>Mathijssen, Ron HJ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymorphisms in</atitle><jtitle>Pharmacogenomics</jtitle><date>2016-09-01</date><risdate>2016</risdate><volume>17</volume><issue>14</issue><spage>1483</spage><epage>1490</epage><pages>1483-1490</pages><issn>1462-2416</issn><eissn>1744-8042</eissn><abstract>Sorafenib-treated patients display a substantial variation in the incidence of toxicity. We aimed to investigate the association of genetic polymorphisms with observed toxicity on sorafenib.
We genotyped 114 patients that were treated with sorafenib at the Erasmus MC Cancer Institute, the Netherlands, for
and
.
The
(rs8175347) polymorphism was associated with hyperbilirubinemia and treatment interruption. Polymorphisms in
(rs2306283, rs4149056) were associated with diarrhea and thrombocytopenia, respectively. None of the investigated polymorphisms was associated with overall or progression-free survival in hepatocellular cancer patients.
Polymorphisms in
and
are associated with several different sorafenib side effects.</abstract><pub>Future Medicine Ltd</pub><doi>10.2217/pgs-2016-0063</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1462-2416 |
ispartof | Pharmacogenomics, 2016-09, Vol.17 (14), p.1483-1490 |
issn | 1462-2416 1744-8042 |
language | eng |
recordid | cdi_futurescience_futuremedicine_10_2217_pgs_2016_0063 |
source | PubMed |
subjects | drug transporters hepatocellular carcinoma pharmacogenetics renal cell cancer sorafenib toxicity |
title | Polymorphisms in |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T10%3A30%3A54IST&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=Polymorphisms%20in&rft.jtitle=Pharmacogenomics&rft.au=Bins,%20Sander&rft.date=2016-09-01&rft.volume=17&rft.issue=14&rft.spage=1483&rft.epage=1490&rft.pages=1483-1490&rft.issn=1462-2416&rft.eissn=1744-8042&rft_id=info:doi/10.2217/pgs-2016-0063&rft_dat=%3Cfuturescience%3E10_2217_pgs_2016_0063%3C/futurescience%3E%3Cgrp_id%3Ecdi_FETCH-futurescience_futuremedicine_10_2217_pgs_2016_00633%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 |