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                  <mods:namePart>Miguelañez</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-01-23T13:27:23Z</mods:dateAccessioned>
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               <mods:identifier type="citation">Ann Oncol. 2016 Sep;27(9):1788-93.</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/17262</mods:identifier>
               <mods:identifier type="pubmedID">27287205</mods:identifier>
               <mods:identifier type="doi">10.1093/annonc/mdw234</mods:identifier>
               <mods:identifier type="e-issn">1569-8041</mods:identifier>
               <mods:identifier type="journal">Annals of oncology : official journal of the European Society for Medical Oncology</mods:identifier>
               <mods:abstract>Background: Despite the effectiveness of current treatment protocols for Ewing sarcoma (ES), many patients still experience relapse, and survival following recurrence is &lt;15%. We aimed to identify genetic variants that predict treatment outcome in children diagnosed with ES. Patients and methods: We carried out a pharmacogenetic study of 384 single-nucleotide polymorphisms (SNPs) in 24 key transport or metabolism genes relevant to drugs used to treat in pediatric patients (&lt;30 years) with histologically confirmed ES. We studied the association of genotypes with tumor response and overall survival (OS) in a discovery cohort of 106 Spanish children, with replication in a second cohort of 389 pediatric patients from across Europe. Results: We identified associations with OS (P &lt; 0.05) for three SNPs in the Spanish cohort that were replicated in the European cohort. The strongest association observed was with rs7190447, located in the ATP-binding cassette subfamily C member 6 (ABCC6) gene [discovery: hazard ratio (HR) = 14.30, 95% confidence interval (CI) = 1.53-134, P = 0.020; replication: HR = 9.28, 95% CI = 2.20-39.2, P = 0.0024] and its correlated SNP rs7192303, which was predicted to have a plausible regulatory function. We also replicated associations with rs4148737 in the ATP-binding cassette subfamily B member 1 (ABCB1) gene (discovery: HR = 2.96, 95% CI = 1.08-8.10, P = 0.034; replication: HR = 1.60, 95% CI = 1.05-2.44, P = 0.029), which we have previously found to be associated with poorer OS in pediatric osteosarcoma patients, and rs11188147 in cytochrome P450 family 2 subfamily C member 8 gene (CYP2C8) (discovery : HR = 2.49, 95% CI = 1.06-5.87, P = 0.037; replication: HR = 1.77, 95% CI = 1.06-2.96, P = 0.030), an enzyme involved in the oxidative metabolism of the ES chemotherapeutic agents cyclophosphamide and ifosfamide. None of the associations with tumor response were replicated. Conclusion: Using an integrated pathway-based approach, we identified polymorphisms in ABCC6, ABCB1 and CYP2C8 associated with OS. These associations were replicated in a large independent cohort, highlighting the importance of pharmacokinetic genes as prognostic markers in ES.</mods:abstract>
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                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:subject>
                  <mods:topic>Ewing sarcoma</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Polymorphisms</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Pharmacokinetic genes</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Prognostic</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Pathway-based approach</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Identification of genetic variants in pharmacokinetic genes associated with Ewing Sarcoma treatment outcome</mods:title>
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               <mods:genre>research article</mods:genre>
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