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ABSTRACT: Background
Cell-free DNA (cfDNA) from plasma offers easily obtainable material for KRAS mutation analysis. Novel, multiplex, and accurate diagnostic systems using small amounts of DNA are needed to further the use of plasma cfDNA testing in personalized therapy.Patients and methods
Samples of 16 ng of unamplified plasma cfDNA from 121 patients with diverse progressing advanced cancers were tested with a KRASG12/G13 multiplex assay to detect the seven most common mutations in the hotspot of exon 2 using droplet digital polymerase chain reaction (ddPCR). The results were retrospectively compared to mutation analysis of archival primary or metastatic tumor tissue obtained at different points of clinical care.Results
Eighty-eight patients (73%) had KRASG12/G13 mutations
SUBMITTER: Janku F
PROVIDER: S-EPMC5834133 | biostudies-literature | 2017 Mar
REPOSITORIES: biostudies-literature