Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/105823
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dc.contributor.authorDelgado-García, Mercedes-
dc.contributor.authorWeynand, Birgit-
dc.contributor.authorGómez-Izquierdo, Lourdes-
dc.contributor.authorHernández, María José-
dc.contributor.authorBlanco, Ángela María-
dc.contributor.authorVarela, Mar-
dc.contributor.authorMatias-Guiu, Xavier-
dc.contributor.authorNadal, Ernest-
dc.contributor.authorMárquez-Lobo, Bélgica-
dc.contributor.authorAlarcão, Ana-
dc.contributor.authorde Álava, Enrique-
dc.contributor.authorBiscuola, Michele-
dc.date.accessioned2023-03-09T12:14:34Z-
dc.date.available2023-03-09T12:14:34Z-
dc.date.issued2020-
dc.identifier.issn1471-2407pt
dc.identifier.urihttps://hdl.handle.net/10316/105823-
dc.description.abstractBackground: Detection of epidermal growth factor receptor (EGFR) mutations in exons 18–21 is recommended in all patients with advanced Non-small-cell lung carcinoma due to the demonstrated efficiency of the standard therapy with tyrosine kinase inhibitors in EGFR-mutated patients. Therefore, choosing a suitable technique to test EGFR mutational status is crucial to warrant a valid result in a short turnaround time using the lowest possible amount of tissue material. The Idylla™ EGFR Mutation Test is a simple, fast and reliable method designed for the detection of EGFR mutations from formalin-fixed paraffin-embedded samples. The aim of this study was the Clinical Performace Evaluation of the Idylla™ EGFR Mutation Test on the Idylla™ System. Methods: EGFR mutational status was determined on 132 archived formalin-fixed paraffin-embedded tissue sections with Idylla™ technology. Results were compared with the results previously obtained by routine method in the reference lab (Therascreen® EGFR RGQ PCR v2, Qiagen in Molecular Pathology lab, Hospital Universitario Virgen del Rocío de Sevilla). Results: The overall agreement between results obtained with the Idylla™ EGFR Mutation Test and the Comparator test method was 95.38% (with 1-sided 95% lower limit of 91.7%) showing Positive Diagnostic Agreement of 93.22% and Negative Diagnostic Agreement of 97.18%, with a Limit Of Detection ≤5%. Conclusions: The Idylla™ EGFR Mutation Test passed its clinical validity performance characteristics for accuracy.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relationSupported by each clinical center. Biocartis provided free-of-charge Idylla™ EGFR Mutation Test cartridges.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectNon-small-cell lung carcinomapt
dc.subjectEGFRpt
dc.subjectMutationspt
dc.titleClinical performance evaluation of the Idylla™ EGFR Mutation Test on formalin-fixed paraffin-embedded tissue of non-small cell lung cancerpt
dc.typearticle-
degois.publication.firstPage275pt
degois.publication.issue1pt
degois.publication.titleBMC Cancerpt
dc.peerreviewedyespt
dc.identifier.doi10.1186/s12885-020-6697-7pt
degois.publication.volume20pt
dc.date.embargo2020-01-01*
uc.date.periodoEmbargo0pt
item.openairetypearticle-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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