Evaluation of the Idylla KRAS and NRAS mutation test in colorectal cancer tissue

被引:7
作者
Zekri, Jamal [1 ]
Baghdadi, Mohammed A. [2 ]
Alardati, Hosam [3 ]
Khallaf, Hamoud [4 ]
Kabanja, Juma H. [4 ]
机构
[1] Alfaisal Univ, Coll Med, King Faisal Specialist Hosp & Res Ctr Jeddah, POB 40047,MBC J-64, Jeddah 21499, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Res Ctr, Jeddah, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Pathol Dept, Jeddah, Saudi Arabia
[4] King Fahad Specialist Hosp, Dept Pathol & Lab Med, Dammam, Saudi Arabia
关键词
Colorectal cancer; KRAS; NRAS; Idylla; 1ST-LINE TREATMENT; POOLED ANALYSIS; RAS MUTATIONS; BRAF; FOLFOX4; SYSTEM;
D O I
10.1016/j.yexmp.2019.104270
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction: The currently approved techniques for RAS mutations testing in colorectal cancer (CRC) tissue are labor-intensive and time consuming. The Idylla technology (IT) is a rapid and fully automated diagnostics system. The primary aim of this study is to compare the Idylla performance against that of conventional techniques (CT). Methodology: Archival CRC tumor samples from 2 hospitals were tested for KRAS and NRAS mutations using the IT. Results were compared to those obtained earlier by CT performed in accredited laboratories. Unexplained discordant results were verified locally by next generation sequencing (NGS) to ascertain the accuracy of IT. Results: Forty five samples were processed. All samples underwent dual testing (CT & IT) for KRAS mutations. IT identified mutations in 2 samples that were not detected by CT. Primary concordance rate for KRAS was 93.3% and the accuracy rate improved to 100% after verification and explanation of discordant results. Only 18 samples underwent dual testing for NRAS. Primary concordance and accuracy rates for NRAS were 94.4%. The mean time from dispatching the specimen for RAS testing by CT until receipt of results was 12 (7-28) days compared to few hours when IT was used. Conclusion: IT provides a quick and reliable mean for RAS testing. In addition, it identifies mutations that are not detected by CT and thus may provide better guidance to treatment choices.
引用
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页数:6
相关论文
共 24 条
[1]   Rapid Somatic Mutation Testing in Colorectal Cancer by Use of a Fully Automated System and Single-Use Cartridge: A Comparison with Next-Generation Sequencing [J].
Al-Turkmani, M. Rabie ;
Godwin, Kelley N. ;
Peterson, Jason D. ;
Tsongalis, Gregory J. .
JOURNAL OF APPLIED LABORATORY MEDICINE, 2018, 3 (02) :178-184
[2]  
[Anonymous], SAUD CANC REG 2015
[3]   Global patterns and trends in colorectal cancer incidence and mortality [J].
Arnold, Melina ;
Sierra, Monica S. ;
Laversanne, Mathieu ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin ;
Bray, Freddie .
GUT, 2017, 66 (04) :683-691
[4]   FOLFOX4 plus cetuximab treatment and RAS mutations in colorectal cancer [J].
Bokemeyer, C. ;
Koehne, C. -H. ;
Ciardiello, F. ;
Lenz, H. -J. ;
Heinemann, V. ;
Klinkhardt, U. ;
Beier, F. ;
Duecker, K. ;
van Krieken, J. H. ;
Tejpar, S. .
EUROPEAN JOURNAL OF CANCER, 2015, 51 (10) :1243-1252
[5]   Validating a fully automated real-time PCR-based system for use in the molecular diagnostic analysis of colorectal carcinoma: a comparison with NGS and IHC [J].
Colling, Richard ;
Wang, Lai Mun ;
Soilleux, Elizabeth .
JOURNAL OF CLINICAL PATHOLOGY, 2017, 70 (07) :610-614
[6]  
Cree Ian A, 2016, Biomol Detect Quantif, V8, P29, DOI 10.1016/j.bdq.2016.05.001
[7]   Final results from PRIME: randomized phase III study of panitumumab with FOLFOX4 for first-line treatment of metastatic colorectal cancer [J].
Douillard, J. Y. ;
Siena, S. ;
Cassidy, J. ;
Tabernero, J. ;
Burkes, R. ;
Barugel, M. ;
Humblet, Y. ;
Bodoky, G. ;
Cunningham, D. ;
Jassem, J. ;
Rivera, F. ;
Kocakova, I. ;
Ruff, P. ;
Blasinska-Morawiec, M. ;
Smakal, M. ;
Canon, J. L. ;
Rother, M. ;
Oliner, K. S. ;
Tian, Y. ;
Xu, F. ;
Sidhu, R. .
ANNALS OF ONCOLOGY, 2014, 25 (07) :1346-1355
[8]   Cetuximab-based therapy for metastatic colorectal cancer: a meta-analysis of the effect of K-ras mutations [J].
Ibrahim, Ezzeldin M. ;
Zekri, Jamal M. ;
Bin Sadiq, Bakr M. .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2010, 25 (06) :713-721
[9]   Clinical performance evaluation of the Idylla NRAS-BRAF mutation test on retrospectively collected formalin-fixed paraffin-embedded colorectal cancer tissue [J].
Johnston, Louise ;
Power, Michael ;
Sloan, Philip ;
Long, Anna ;
Silmon, Angela ;
Chaffey, Ben ;
Lisgo, Andrea Jane ;
Little, Liam ;
Vercauteren, Ellen ;
Steiniche, Torben ;
Meyer, Tine ;
Simpson, John .
JOURNAL OF CLINICAL PATHOLOGY, 2018, 71 (04) :336-343
[10]   Financial implications of Idylla testing in colorectal cancer, lung cancer and melanoma: a French laboratory point of view [J].
Le Flahec, Glen ;
Guibourg, Briac ;
Marcorelles, Pascale ;
Uguen, Arnaud .
JOURNAL OF CLINICAL PATHOLOGY, 2017, 70 (10) :906-907