Comparison of Tissue Molecular Biomarker Testing Turnaround Times and Concordance Between Standard of Care and the Biocartis Idylla Platform in Patients With Colorectal Cancer. Issue 2 (11th June 2020)
- Record Type:
- Journal Article
- Title:
- Comparison of Tissue Molecular Biomarker Testing Turnaround Times and Concordance Between Standard of Care and the Biocartis Idylla Platform in Patients With Colorectal Cancer. Issue 2 (11th June 2020)
- Main Title:
- Comparison of Tissue Molecular Biomarker Testing Turnaround Times and Concordance Between Standard of Care and the Biocartis Idylla Platform in Patients With Colorectal Cancer
- Authors:
- Tsongalis, Gregory J
Al Turkmani, M Rabie
Suriawinata, Michael
Babcock, Michael J
Mitchell, Kristi
Ding, Yi
Scicchitano, Lisa
Tira, Adrian
Buckingham, Lela
Atkinson, Sara
Lax, Amy
Aisner, Dara L
Davies, Kurtis D
Wood, Holly N
O'Neill, Stacey S
Levine, Edward A
Sequeira, Judy
Harada, Shuko
DeFrank, Gina
Paluri, Ravikumar
Tan, Bradford A
Colabella, Heather
Snead, Christopher
Cruz-Correa, Marcia
Ramirez, Virginia
Rojas, Arnaldo
Huang, Huiya
Mackinnon, Alexander C
Garcia, Fernando U
Cavone, Sharon M
Elfahal, Mutasim
Abel, Gyorgy
Vasef, Mohammad A
Judd, Andrew
Linder, Mark W
Alkhateeb, Khaled
Skinner, William L
Boccia, Ralph
Patel, Kashyap
… (more) - Abstract:
- 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 clinicalAbstract: 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. … (more)
- Is Part Of:
- American journal of clinical pathology. Volume 154:Issue 2(2020)
- Journal:
- American journal of clinical pathology
- Issue:
- Volume 154:Issue 2(2020)
- Issue Display:
- Volume 154, Issue 2 (2020)
- Year:
- 2020
- Volume:
- 154
- Issue:
- 2
- Issue Sort Value:
- 2020-0154-0002-0000
- Page Start:
- 266
- Page End:
- 276
- Publication Date:
- 2020-06-11
- Subjects:
- Colorectal cancer -- Molecular pathology -- Precision medicine -- KRAS -- NRAS -- BRAF
Diagnosis, Laboratory -- Periodicals
Pathology -- Periodicals
616.07 - Journal URLs:
- http://www.oxfordjournals.org/ ↗
http://ajcp.oxfordjournals.org/ ↗ - DOI:
- 10.1093/ajcp/aqaa044 ↗
- Languages:
- English
- ISSNs:
- 0002-9173
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0824.000000
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- 15443.xml