| Literature DB >> 26921540 |
Ana-Iris Schiefer1, Laura Parlow2, Lisa Gabler1, Ildiko Mesteri3, Oskar Koperek1, Andreas von Deimling4, Berthold Streubel5, Matthias Preusser6, Annika Lehmann2, Udo Kellner7, Patrick Pauwels8, Suzan Lambin8, Manfred Dietel2, Michael Hummel9, Frederick Klauschen2, Peter Birner10, Markus Möbs2.
Abstract
The mutated BRAF oncogene represents a therapeutic target in malignant melanoma. Because BRAF mutations are also involved in the pathogenesis of other human malignancies, the use of specific BRAF inhibitors might also be extended to other diseases in the future. A prerequisite for the clinical application of BRAF inhibitors is the reliable detection of activating BRAF mutations in routine histopathological samples. In a multicenter approach, we evaluated a novel and fully automated PCR-based system (Idylla) capable of detecting BRAF V600 mutations in formalin-fixed, paraffin-embedded tissue within 90 minutes with high sensitivity. We analyzed a total of 436 samples with the Idylla system. Valid results were obtained in 421 cases (96.56%). Its performance was compared with conventional methods (pyrosequencing or Sanger sequencing). Concordant results were obtained in 406 cases (96.90%). Reanalysis of eight discordant samples by next-generation sequencing and/or pyrosequencing with newly extracted DNA and the BRAF RGQ Kit confirmed the Idylla result in seven cases, resulting in an overall agreement of 98.57%. In conclusion, the Idylla system is a highly reliable and sensitive platform for detection of BRAF V600 mutations in formalin-fixed, paraffin-embedded material, providing an efficient alternative to conventional diagnostic methods, particularly for routine diagnostics laboratories with limited experience in molecular pathology.Entities:
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Year: 2016 PMID: 26921540 DOI: 10.1016/j.jmoldx.2015.12.005
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568