| Literature DB >> 29959022 |
Iván Prieto-Potin1, Clara Montagut2, Beatriz Bellosillo3, Matthew Evans4, Matthew Smith4, Linea Melchior5, Werner Reiltin6, Michael Bennett6, Veronica Pennati7, Francesca Castiglione7, Karl-Friedrich Bürrig8, Ulrike Cooper8, Barbara Dockhorn-Dworniczak9, Christiana Rossenbach9, Claudia M Luna-Aguirre10, Hugo A Barrera-Saldaña10, José C Machado11, José L Costa11, Rinat Yacobi12, Hilla Tabibian-Keissar12, Simonetta Buglioni13, Livia Ronchetti13, Lotte Douglas-Berger14, Hendrikus J Dubbink14, Mohammed Alorini15, Jean-Christophe Sabourin15, Federico Rojo16.
Abstract
Treatment of colorectal cancer (CRC) with monoclonal antibodies against epidermal growth factor receptor requires the assessment of the mutational status of exons 2, 3, and 4 of the NRAS and KRAS oncogenes. Moreover, the mutational status of exon 15 of the BRAF oncogene is a marker of poor prognosis in CRC. The Idylla NRAS-BRAF Mutation Test is a reliable, simple (<2 minutes hands-on time), and quick (<2 hours turnaround time) sample-to-result solution, enabling the detection of clinically relevant mutations in NRAS (18 mutations) and BRAF (5 mutations). A multicenter study was conducted in 14 centers using the Idylla NRAS-BRAF Mutation Test to assess the NRAS and BRAF mutational status of 418 formalin-fixed, paraffin-embedded tissue samples from CRC patients. Results were compared with those obtained earlier by routine reference methods, including next-generation sequencing, pyrosequencing, mass spectrometry-based assays, PCR-based assays, and Sanger sequencing. In case of discordance, additional tests were performed by digital droplet PCR. Overall, after testing confirmation and excluding invalids/errors by design, concordances between the Idylla NRAS-BRAF Mutation Test and the reference test results were found in almost perfect agreement. In conclusion, the Idylla NRAS-BRAF Mutation Test enables the routine detection of all NRAS and BRAF mutations deemed clinically relevant according to the latest clinical guidelines, without necessitating molecular expertise or infrastructure.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29959022 DOI: 10.1016/j.jmoldx.2018.05.008
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568