<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-31T16:52:50Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/25285" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/25285</identifier><datestamp>2024-10-23T13:07:25Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16958</setSpec><setSpec>col_20.500.12105_16962</setSpec><setSpec>col_20.500.12105_16986</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Delgado-García, Mercedes</subfield>
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      <subfield code="a">Weynand, Birgit</subfield>
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      <subfield code="a">Gómez-Izquierdo, Lourdes</subfield>
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      <subfield code="a">Hernández, María José</subfield>
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      <subfield code="a">Blanco, Ángela María</subfield>
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      <subfield code="a">Varela, Mar</subfield>
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      <subfield code="a">Matias-Guiu, Xavier</subfield>
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      <subfield code="a">Nadal, Ernest</subfield>
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      <subfield code="a">Márquez-Lobo, Bélgica</subfield>
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      <subfield code="a">Alarcão, Ana</subfield>
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      <subfield code="a">de Álava, Enrique</subfield>
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      <subfield code="a">Biscuola, Michele</subfield>
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      <subfield code="c">2020-04-03</subfield>
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      <subfield code="a">Background: 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.</subfield>
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      <subfield code="a">10.1186/s12885-020-6697-7</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/25285</subfield>
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      <subfield code="a">EGFR</subfield>
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      <subfield code="a">Clinical performance evaluation of the Idylla™ EGFR Mutation Test on formalin-fixed paraffin-embedded tissue of non-small cell lung cancer</subfield>
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