TY - JOUR
T1 - Multicenter Evaluation of the Idylla NRAS-BRAF Mutation Test in Metastatic Colorectal Cancer
AU - Prieto-Potin, Iván
AU - Montagut, Clara
AU - Bellosillo, Beatriz
AU - Evans, Matthew
AU - Smith, Matthew
AU - Melchior, Linea
AU - Reiltin, Werner
AU - Bennett, Michael
AU - Pennati, Veronica
AU - Castiglione, Francesca
AU - Bürrig, Karl-Friedrich
AU - Cooper, Ulrike
AU - Dockhorn-Dworniczak, Barbara
AU - Rossenbach, Christiana
AU - Luna-Aguirre, Claudia M
AU - Barrera-Saldaña, Hugo A
AU - Machado, José C
AU - Costa, José L
AU - Yacobi, Rinat
AU - Tabibian-Keissar, Hilla
AU - Buglioni, Simonetta
AU - Ronchetti, Livia
AU - Douglas-Berger, Lotte
AU - Dubbink, Hendrikus J
AU - Alorini, Mohammed
AU - Sabourin, Jean-Christophe
AU - Rojo, Federico
N1 - Copyright © 2018 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved.
PY - 2018/9
Y1 - 2018/9
N2 - 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.
AB - 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.
U2 - 10.1016/j.jmoldx.2018.05.008
DO - 10.1016/j.jmoldx.2018.05.008
M3 - Journal article
C2 - 29959022
SN - 1525-1578
VL - 20
SP - 664
EP - 676
JO - The Journal of molecular diagnostics : JMD
JF - The Journal of molecular diagnostics : JMD
IS - 5
ER -