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Lung cancer mutation testing: a clinical retesting study of agreement between a real-time PCR and a mass spectrometry test.

Authors :
Shepherd P
Sheath KL
Tin ST
Khwaounjoo P
Aye PS
Li A
Laking GR
Kingston NJ
Lewis CA
Mark Elwood J
Love DR
McKeage MJ
Source :
Oncotarget [Oncotarget] 2017 Sep 16; Vol. 8 (60), pp. 101437-101451. Date of Electronic Publication: 2017 Sep 16 (Print Publication: 2017).
Publication Year :
2017

Abstract

To investigate the clinical validity and utility of tests for detecting Epidermal Growth Factor Receptor ( EGFR ) gene mutations in non-squamous non-small cell lung cancer patients, tumour DNA extracts from 532 patients previously tested by the cobas EGFR Mutation Test (RT-PCR test) were retested by the Sequenom/Agena Biosciences MassArray OncoFocus mass spectrometry test (MS test). Valid results from both tests were available from 470 patients (88%) for agreement analysis. Survival data were obtained for 513 patients (96%) and 77 patients (14%) were treated with EGFR tyrosine kinase inhibitors (TKIs). Agreement analysis revealed moderately high positive (79.8%), negative (96.9%) and overall percentage agreement (93.2%) for the detection of EGFR mutations. However, EGFR mutations were detected by one test and not by the other test in 32 patients (7%). Retesting of discordant samples revealed false-positive and false-negative results generated by both tests. Despite this, treatment and survival outcomes correlated with the results of the RT-PCR and MS tests. In conclusion, this study provides evidence of the clinical validity and utility of the RT-PCR and MS tests for detection of EGFR mutations that predict prognosis and benefit from EGFR-TKI treatment. However, their false-positive and false-negative test results may have important clinical consequences.<br />Competing Interests: CONFLICTS OF INTEREST The authors report no conflicts of interest.

Details

Language :
English
ISSN :
1949-2553
Volume :
8
Issue :
60
Database :
MEDLINE
Journal :
Oncotarget
Publication Type :
Academic Journal
Accession number :
29254176
Full Text :
https://doi.org/10.18632/oncotarget.21023