Fully automated real-time PCR for EGFR testing in non-small cell lung carcinoma.


Journal

Virchows Archiv : an international journal of pathology
ISSN: 1432-2307
Titre abrégé: Virchows Arch
Pays: Germany
ID NLM: 9423843

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 17 07 2018
accepted: 13 11 2018
revised: 23 10 2018
pubmed: 25 11 2018
medline: 21 3 2019
entrez: 25 11 2018
Statut: ppublish

Résumé

Molecular testing for mutations in the EGFR gene is commonplace for patients with non-small cell lung cancer (NSCLC). These patients are often very sick and management decisions need to be made urgently. In many cases, the results of molecular testing are needed the same day, in order to start targeted therapy and allow maximum benefit for patients. The Idylla™ EGFR Mutation Test offers rapid results within three hours of requesting. This study aimed to assess the concordance of Idylla™ EGFR Mutation Test results with current standard tests. Forty formalin-fixed, paraffin-embedded NSCLC tumour cases (20 EGFR mutant and EGFR 20 wild type) were analysed by the Idylla™ EGFR Mutation Test (CE-IVD) and compared with PCR and NGS methodologies. The overall concordance between Idylla™ and standard testing was 92.5% (95% CI 80.14% to 97.42%) and the specificity of Idylla™ was 100% (95% CI 83.89% to 100%). The sensitivity was affected by loss of tumour content in tissue blocks in a small number of NGS cases; however, comparing Idylla™ with PCR alone, there was 100% concordance (95% CI 89.85% to 100%). The Idylla™ EGFR Mutation Test shows comparative accuracy to routine PCR testing for the most common EGFR mutations in NSCLC. The Idylla™ also offers significantly reduced turn-around times compared with existing modalities and therefore the platform would be a useful addition to many molecular diagnostics units.

Identifiants

pubmed: 30470932
doi: 10.1007/s00428-018-2486-y
pii: 10.1007/s00428-018-2486-y
pmc: PMC6349793
doi:

Substances chimiques

EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

187-192

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Auteurs

Richard Colling (R)

Nuffield Division of Clinical Laboratory Sciences, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, UK. richard.colling@ndcls.ox.ac.uk.
Department of Cellular Pathology, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, OX3 9DU, UK. richard.colling@ndcls.ox.ac.uk.

Hollie Bancroft (H)

Department of Histopathology, Birmingham Heartlands Hospital, Heart of England NHS Foundation Trust, Bordesley Green Estate, Birmingham, B9 5SS, UK.

Gerald Langman (G)

Department of Histopathology, Birmingham Heartlands Hospital, Heart of England NHS Foundation Trust, Bordesley Green Estate, Birmingham, B9 5SS, UK.

Elizabeth Soilleux (E)

Division of Cellular and Molecular Pathology, Addenbrooke's Hospital, Lab Block Level 3, Box 231, Cambridge, CB2 0QQ, UK.

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Classifications MeSH