Comparison of 2 Commercially Available Next-Generation Sequencing Platforms in Oncology

Nicole M. Kuderer(University of Washington), Kimberly A. Burton(University of Washington), Sibel Blau(Northwest Medical Specialties), Andrea L. Rose(Northwest Medical Specialties), Stephanie Parker(Northwest Medical Specialties), Gary H. Lyman(Fred Hutch Cancer Center), C. Anthony Blau(University of Washington)
JAMA Oncology
December 19, 2016
Cited by 171Open Access
Full Text

Abstract

The growing use of next generation-sequencing to identify cancer-associated alterations as well as the increasing number of targeted drugs holds promise for better matching patients with cancer with effective therapies. The FoundationOne (F1; Foundation Medicine) test sequences clinical tumor samples to characterize the exons of 315 cancer-associated genes and introns from 28 genes involved in rearrangements. The Guardant360 (G360; Guardant Health) test uses cell-free circulating DNA from blood to sequence 70 genes. Both the F1 and G360 tests have high specificities (>99%) and somewhat lower sensitivities. 1,2 However, little is known about how different next-generation sequencing tests compare when used in the same patients with cancer. We compared reports from F1 and G360 testing in 9 patients from a community oncology practice to determine the level of concordance between the platforms.


Related Papers