Comparison of Biocartis IDYLLA ™ cartridge assay with Qiagen GeneReader NGS for detection of targetable mutations in EGFR, KRAS/NRAS, and BRAF genes
Lung and colorectal cancers (CRC) have two of the highest mortality rates among all cancer types, and their occurrence and the need for personalized diagnostics and subsequent therapy were not influenced by the COVID-19 pandemics. However, due to the disruption of established delivery chains, standa...
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Veröffentlicht in: | Experimental and molecular pathology 2021-06, Vol.120, p.104634-104634, Article 104634 |
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creator | Haiduk, Tiffany Brockmann, Michael Tillmann, Ramona-Liza Pieper, Monika Lüsebrink, Jessica Schildgen, Verena Schildgen, Oliver |
description | Lung and colorectal cancers (CRC) have two of the highest mortality rates among all cancer types, and their occurrence and the need for personalized diagnostics and subsequent therapy were not influenced by the COVID-19 pandemics. However, due to the disruption of established delivery chains, standard assays for in vitro diagnostics of those cancers were temporarily not available, forcing us to implement alternative testing methods that enabled at least basic therapy decision making. For this reason, we evaluated rapid testing on the Biocartis Idylla™ platform (Biocartis, Mechelen, Belgium) for four important genes commonly mutated in lung and colorectal cancers, namely EGFR, NRAS, KRAS, and BRAF. Clinical specimens from which the mutation status has previously been determined using Next Generation Sequencing (NGS), were retested to determine whether Idylla™ can offer accurate results. To compare the results, the sensitivity, specificity, positive predictive values (PPV) and negative predictive values (NPV) are calculated for each of the mutation types and then combined to determine the values of the Idylla™ system in total, while setting NGS as the gold-standard basis the assays were compared with. Idylla testing thereby displayed acceptable sensitivity and specificity and delivered reliable results for initial therapy decisions. |
doi_str_mv | 10.1016/j.yexmp.2021.104634 |
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However, due to the disruption of established delivery chains, standard assays for in vitro diagnostics of those cancers were temporarily not available, forcing us to implement alternative testing methods that enabled at least basic therapy decision making. For this reason, we evaluated rapid testing on the Biocartis Idylla™ platform (Biocartis, Mechelen, Belgium) for four important genes commonly mutated in lung and colorectal cancers, namely EGFR, NRAS, KRAS, and BRAF. Clinical specimens from which the mutation status has previously been determined using Next Generation Sequencing (NGS), were retested to determine whether Idylla™ can offer accurate results. To compare the results, the sensitivity, specificity, positive predictive values (PPV) and negative predictive values (NPV) are calculated for each of the mutation types and then combined to determine the values of the Idylla™ system in total, while setting NGS as the gold-standard basis the assays were compared with. Idylla testing thereby displayed acceptable sensitivity and specificity and delivered reliable results for initial therapy decisions.</description><identifier>ISSN: 0014-4800</identifier><identifier>EISSN: 1096-0945</identifier><identifier>DOI: 10.1016/j.yexmp.2021.104634</identifier><identifier>PMID: 33773991</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>BRAF ; COVID-19 ; CRC ; Delivery chain interruptions ; EGFR ; KRAS ; Lung cancer ; NRAS ; Personalized diagnostics</subject><ispartof>Experimental and molecular pathology, 2021-06, Vol.120, p.104634-104634, Article 104634</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. 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Idylla testing thereby displayed acceptable sensitivity and specificity and delivered reliable results for initial therapy decisions.</description><subject>BRAF</subject><subject>COVID-19</subject><subject>CRC</subject><subject>Delivery chain interruptions</subject><subject>EGFR</subject><subject>KRAS</subject><subject>Lung cancer</subject><subject>NRAS</subject><subject>Personalized diagnostics</subject><issn>0014-4800</issn><issn>1096-0945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kcFuEzEQhi0EoqHwBEhojhy66djr9a4PHNLQhIqoiBQOnCxndzY4yu6m9gaae5-BB-DReBIctnDkMh79-ucfjT_GXnIcc-TqfDM-0F2zGwsUPCpSpfIRG3HUKkEts8dshMhlIgvEE_YshA0iauTiKTtJ0zxPteYj9mPaNTvrXeha6Gq4cF1pfe8CXL39slhM4Nf9Tzgq3lVrAhuCPcB313-Fj86uqYU5tbQkW5GH6_kN1J2HinoqezcE9tavqberLUGz7-1RDuBauJzPlmfwfjm5Ob-O5QxsW8HFcjKDmErhOXtS222gFw_vKfs8u_w0fZcsPsyvppNFUopc9omuc9JVFm9fYexzZVGvKpmLQsiaK5UVhcyVJC4sKpXWKs1JEIoy14WVmU5P2eshd-e72z2F3jQulLTd2pa6fTAiQxXjMy6jNR2spe9C8FSbnXeN9QfD0RyBmI35A8QcgZgBSJx69bBgv2qo-jfzl0A0vBkMFM_85sibUDpqS6qcj99oqs79d8Fv3xabnA</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Haiduk, Tiffany</creator><creator>Brockmann, Michael</creator><creator>Tillmann, Ramona-Liza</creator><creator>Pieper, Monika</creator><creator>Lüsebrink, Jessica</creator><creator>Schildgen, Verena</creator><creator>Schildgen, Oliver</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210601</creationdate><title>Comparison of Biocartis IDYLLA ™ cartridge assay with Qiagen GeneReader NGS for detection of targetable mutations in EGFR, KRAS/NRAS, and BRAF genes</title><author>Haiduk, Tiffany ; Brockmann, Michael ; Tillmann, Ramona-Liza ; Pieper, Monika ; Lüsebrink, Jessica ; Schildgen, Verena ; Schildgen, Oliver</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-9f7e9d5046b09f776a09bd472824f1665884764e12a0663f637e2e02c798a4593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>BRAF</topic><topic>COVID-19</topic><topic>CRC</topic><topic>Delivery chain interruptions</topic><topic>EGFR</topic><topic>KRAS</topic><topic>Lung cancer</topic><topic>NRAS</topic><topic>Personalized diagnostics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haiduk, Tiffany</creatorcontrib><creatorcontrib>Brockmann, Michael</creatorcontrib><creatorcontrib>Tillmann, Ramona-Liza</creatorcontrib><creatorcontrib>Pieper, Monika</creatorcontrib><creatorcontrib>Lüsebrink, Jessica</creatorcontrib><creatorcontrib>Schildgen, Verena</creatorcontrib><creatorcontrib>Schildgen, Oliver</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental and molecular pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haiduk, Tiffany</au><au>Brockmann, Michael</au><au>Tillmann, Ramona-Liza</au><au>Pieper, Monika</au><au>Lüsebrink, Jessica</au><au>Schildgen, Verena</au><au>Schildgen, Oliver</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of Biocartis IDYLLA ™ cartridge assay with Qiagen GeneReader NGS for detection of targetable mutations in EGFR, KRAS/NRAS, and BRAF genes</atitle><jtitle>Experimental and molecular pathology</jtitle><addtitle>Exp Mol Pathol</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>120</volume><spage>104634</spage><epage>104634</epage><pages>104634-104634</pages><artnum>104634</artnum><issn>0014-4800</issn><eissn>1096-0945</eissn><abstract>Lung and colorectal cancers (CRC) have two of the highest mortality rates among all cancer types, and their occurrence and the need for personalized diagnostics and subsequent therapy were not influenced by the COVID-19 pandemics. 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subjects | BRAF COVID-19 CRC Delivery chain interruptions EGFR KRAS Lung cancer NRAS Personalized diagnostics |
title | Comparison of Biocartis IDYLLA ™ cartridge assay with Qiagen GeneReader NGS for detection of targetable mutations in EGFR, KRAS/NRAS, and BRAF genes |
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