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dc.contributor.authorGreen, H
dc.contributor.authorHasmats, J
dc.contributor.authorKupershmidt, I
dc.contributor.authorEdsgard, D
dc.contributor.authorde Petris, L
dc.contributor.authorLewensohn, R
dc.contributor.authorBlackhall, Fiona H
dc.contributor.authorVikingsson, S
dc.contributor.authorBesse, B
dc.contributor.authorLindgren, A
dc.contributor.authorKoyi, H
dc.contributor.authorBranden, E
dc.contributor.authorPeterson, C
dc.contributor.authorLundeberg, J
dc.date.accessioned2015-10-26T10:42:10Zen
dc.date.available2015-10-26T10:42:10Zen
dc.date.issued2015-09-16en
dc.identifier.citationUsing whole exome sequencing to identify genetic markers for carboplatin and gemcitabine-induced toxicities. 2015: Clin Cancer Resen
dc.identifier.issn1078-0432en
dc.identifier.pmid26378035en
dc.identifier.doi10.1158/1078-0432.CCR-15-0964en
dc.identifier.urihttp://hdl.handle.net/10541/581081en
dc.description.abstractChemotherapies are associated with significant inter-individual variability in therapeutic effect and adverse drug reactions. In lung cancer, the use of gemcitabine and carboplatin induces grade 3 or 4 myelosuppression in about a quarter of the patients, while an equal fraction of patients are basically unaffected in terms of myelosuppressive side effects. We therefore set out to identify genetic markers for gemcitabine/carboplatin-induced myelosuppression.
dc.languageENGen
dc.language.isoenen
dc.rightsArchived with thanks to Clinical cancer research : an official journal of the American Association for Cancer Researchen
dc.titleUsing whole exome sequencing to identify genetic markers for carboplatin and gemcitabine-induced toxicities.en
dc.typeArticleen
dc.contributor.departmentMedical and Health Sciences, Linkoping Universityen
dc.identifier.journalClinical Cancer Researchen
refterms.dateFOA2020-05-01T14:17:04Z
html.description.abstractChemotherapies are associated with significant inter-individual variability in therapeutic effect and adverse drug reactions. In lung cancer, the use of gemcitabine and carboplatin induces grade 3 or 4 myelosuppression in about a quarter of the patients, while an equal fraction of patients are basically unaffected in terms of myelosuppressive side effects. We therefore set out to identify genetic markers for gemcitabine/carboplatin-induced myelosuppression.


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