<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fasching PA</submitter><funding>NCI NIH HHS</funding><pagination>78133-78143</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5652844</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(44)</volume><pubmed_abstract>Hematotoxicity is one of the major side effects of chemotherapy. The aim of this study was to examine the association between single nucleotide polymorphisms (SNPs) and hematotoxicity in breast cancer patients in a subset of patients of the SUCCESS prospective phase III chemotherapy study. All patients (n = 1678) received three cycles of 5-fluorouracil, epirubicin, and cyclophosphamide (FEC) followed by three cycles of docetaxel or docetaxel/gemcitabine, depending on randomization. Germline DNA was genotyped for 246 SNPs selected from a previous genome-wide association study (GWAS) in a panel of lymphoblastoid cell lines, with gemcitabine toxicity as the phenotype. All SNPs were tested for their value in predicting grade 3 or 4 neutropenic or leukopenic events (NLEs). Their prognostic valu</pubmed_abstract><journal>Oncotarget</journal><pubmed_title>Clinical validation of genetic variants associated with &lt;i>in vitro&lt;/i> chemotherapy-related lymphoblastoid cell toxicity.</pubmed_title><pmcid>PMC5652844</pmcid><funding_grant_id>N01 CA015083</funding_grant_id><funding_grant_id>P30 CA015083</funding_grant_id><funding_grant_id>P30 CA076292</funding_grant_id><pubmed_authors>Rezai M</pubmed_authors><pubmed_authors>Jenkins G</pubmed_authors><pubmed_authors>Lichtenegger W</pubmed_authors><pubmed_authors>Ekici AB</pubmed_authors><pubmed_authors>Tesch H</pubmed_authors><pubmed_authors>Heinrich G</pubmed_authors><pubmed_authors>Rack B</pubmed_authors><pubmed_authors>Ruebner M</pubmed_authors><pubmed_authors>Fridley B</pubmed_authors><pubmed_authors>Fehm T</pubmed_authors><pubmed_authors>Lux MP</pubmed_authors><pubmed_authors>Fasching PA</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Reis A</pubmed_authors><pubmed_authors>Beckmann MW</pubmed_authors><pubmed_authors>Cunningham JM</pubmed_authors><pubmed_authors>Haberle L</pubmed_authors><pubmed_authors>Janni W</pubmed_authors><pubmed_authors>Weinshilboum RM</pubmed_authors><pubmed_authors>Hein A</pubmed_authors><pubmed_authors>Schneeweiss A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical validation of genetic variants associated with &lt;i>in vitro&lt;/i> chemotherapy-related lymphoblastoid cell toxicity.</name><description>Hematotoxicity is one of the major side effects of chemotherapy. The aim of this study was to examine the association between single nucleotide polymorphisms (SNPs) and hematotoxicity in breast cancer patients in a subset of patients of the SUCCESS prospective phase III chemotherapy study. All patients (n = 1678) received three cycles of 5-fluorouracil, epirubicin, and cyclophosphamide (FEC) followed by three cycles of docetaxel or docetaxel/gemcitabine, depending on randomization. Germline DNA was genotyped for 246 SNPs selected from a previous genome-wide association study (GWAS) in a panel of lymphoblastoid cell lines, with gemcitabine toxicity as the phenotype. All SNPs were tested for their value in predicting grade 3 or 4 neutropenic or leukopenic events (NLEs). Their prognostic valu</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Sep</publication><modification>2026-04-29T09:55:52.233Z</modification><creation>2019-03-27T02:59:42Z</creation></dates><accession>S-EPMC5652844</accession><cross_references><pubmed>29100455</pubmed><doi>10.18632/oncotarget.17726</doi></cross_references></HashMap>