Literature DB >> 32525522

Comparison of Tissue Molecular Biomarker Testing Turnaround Times and Concordance Between Standard of Care and the Biocartis Idylla Platform in Patients With Colorectal Cancer.

Gregory J Tsongalis1,2, M Rabie Al Turkmani1,2, Michael Suriawinata1,2, Michael J Babcock3, Kristi Mitchell3, Yi Ding4, Lisa Scicchitano4, Adrian Tira5, Lela Buckingham5, Sara Atkinson6, Amy Lax6, Dara L Aisner7, Kurtis D Davies7, Holly N Wood7, Stacey S O'Neill8, Edward A Levine9, Judy Sequeira10, Shuko Harada11, Gina DeFrank11, Ravikumar Paluri12, Bradford A Tan13, Heather Colabella13, Christopher Snead14, Marcia Cruz-Correa15, Virginia Ramirez15, Arnaldo Rojas15, Huiya Huang16, Alexander C Mackinnon16, Fernando U Garcia17, Sharon M Cavone17, Mutasim Elfahal18, Gyorgy Abel18, Mohammad A Vasef19, Andrew Judd19, Mark W Linder20, Khaled Alkhateeb20, William L Skinner21, Ralph Boccia22, Kashyap Patel23.   

Abstract

OBJECTIVES: Management of colorectal cancer warrants mutational analysis of KRAS/NRAS when considering anti-epidermal growth factor receptor therapy and BRAF testing for prognostic stratification. In this multicenter study, we compared a fully integrated, cartridge-based system to standard-of-care assays used by participating laboratories.
METHODS: Twenty laboratories enrolled 874 colorectal cancer cases between November 2017 and December 2018. Testing was performed on the Idylla automated system (Biocartis) using the KRAS and NRAS-BRAF cartridges (research use only) and results compared with in-house standard-of-care testing methods.
RESULTS: There were sufficient data on 780 cases to measure turnaround time compared with standard assays. In-house polymerase chain reaction (PCR) had an average testing turnaround time of 5.6 days, send-out PCR of 22.5 days, in-house Sanger sequencing of 14.7 days, send-out Sanger of 17.8 days, in-house next-generation sequencing (NGS) of 12.5 days, and send-out NGS of 20.0 days. Standard testing had an average turnaround time of 11 days. Idylla average time to results was 4.9 days with a range of 0.4 to 13.5 days.
CONCLUSIONS: The described cartridge-based system offers rapid and reliable testing of clinically actionable mutation in colorectal cancer specimens directly from formalin-fixed, paraffin-embedded tissue sections. Its simplicity and ease of use compared with other molecular techniques make it suitable for routine clinical laboratory testing. © American Society for Clinical Pathology, 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  BRAF; Colorectal cancer; KRAS; Molecular pathology; NRAS; Precision medicine

Year:  2020        PMID: 32525522     DOI: 10.1093/ajcp/aqaa044

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  2 in total

1.  A graphical, interactive and GPU-enabled workflow to process long-read sequencing data.

Authors:  Shishir Reddy; Ling-Hong Hung; Olga Sala-Torra; Jerald P Radich; Cecilia Cs Yeung; Ka Yee Yeung
Journal:  BMC Genomics       Date:  2021-08-23       Impact factor: 4.547

2.  Utility of Select Gene Mutation Detection in Tumors by the Idylla Rapid Multiplex PCR Platform in Comparison to Next-Generation Sequencing.

Authors:  Dingani Nkosi; Vektra L Casler; Chauncey R Syposs; Zoltán N Oltvai
Journal:  Genes (Basel)       Date:  2022-04-29       Impact factor: 4.141

  2 in total

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