Circulating free DNA as biomarker and source for mutation detection in metastatic colorectal cancer

Karen Lise Garm Spindler, Niels Pallisgaard, Rikke Fredslund Andersen, Ivan Brandslund, Anders Jakobsen

Publikation: Bidrag til tidsskriftTidsskriftartikelpeer review

Abstract

Background Circulating cell-free DNA (cfDNA) in plasma has shown potential as biomarker in various cancers and could become an importance source for tumour mutation detection. The objectives of our study were to establish a normal range of cfDNA in a cohort of healthy individuals and to compare this with four cohorts of metastatic colorectal cancer (mCRC) patients. We also investigated the prognostic value of cfDNA and analysed the tumour-specific KRAS mutations in the plasma. Methods The study was a prospective biomarker evaluation in four consecutive Phase II trials, including 229 patients with chemotherapy refractory mCRC and 100 healthy individuals. Plasma was obtained from an EDTA blood-sample, and the total number of DNA alleles and KRAS mutated alleles were assessed using an in-house ARMS-qPCR as previously described. Results Median cfDNA levels were higher in mCRC compared to controls (p < 0.0001). ROC analysis revealed an AUC of 0.9486 (p<0.00001). Data showed impaired OS with increasing levels of baseline cfDNA both when categorising patients by quartiles of cfDNA and into low or high cfDNA groups based on the upper normal range of the control group (Median OS 10.2 (8.3-11.7) and 5.2 (4.6-5.9) months, respectively, HR 1.78, p = 0.0006). Multivariate analysis confirmed an independent prognostic value of cfDNA (HR 1.5 (95% CI 1.3-1.7) for each increase in the cfDNA quartile). The overall concordance of KRAS mutations in plasma and Conclusions These data confirm the prognostic value of cfDNA measurement in plasma and utility for mutation detection with the method presented. tissue was high (85%).

OriginalsprogEngelsk
Artikelnummere0108247
TidsskriftPLOS ONE
Vol/bind10
Udgave nummer4
ISSN1932-6203
DOI
StatusUdgivet - 13 apr. 2015
Udgivet eksterntJa

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