Comparison of KRAS Mutation Assessment in Tumor DNA and Circulating Free DNA in Plasma and Serum Samples
Author(s) -
Shethah Morgan,
Jessica Whiteley,
Emma Donald,
John Smith,
Marcia Eisenberg,
Eddie Kallam,
Lauren Kam-Morgan
Publication year - 2012
Publication title -
clinical medicine insights pathology
Language(s) - English
Resource type - Journals
ISSN - 1179-5557
DOI - 10.4137/cpath.s8798
Subject(s) - kras , colorectal cancer , polymerase chain reaction , circulating tumor dna , oncogene , medicine , dna , cancer , cancer research , oncology , biology , gene , genetics , cell cycle
Testing for mutations in the KRAS oncogene for patients with metastatic colorectal cancer (mCRC) is generally performed using DNA from formalin-fixed paraffin-embedded tumor tissue; however, access to specimens can be limited and analysis challenging. This study assessed the identification of KRAS mutations in circulating free DNA (cfDNA) using a commercially available KRAS polymerase chain reaction (PCR) kit. Matched plasma, serum and tumor samples were available from 71 patients with mCRC who had received prior therapy but whose disease progressed following therapy. Yields of cfDNA from plasma and serum samples were comparable. Analyses were successful in 70/71 plasma-extracted samples (specificity: 97%, sensitivity: 31%) and 67/71 serum- extracted samples (specificity: 100%, sensitivity: 25%). This study demonstrates that KRAS mutations can be detected in cfDNA using a commercially available KRAS PCR kit, confirming cfDNA as a potential alternative source of tumor DNA in a diagnostic setting if access to archival tumor specimens is limited.
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