Table 1.
Primary analysis population (N = 155)a | |||||||
---|---|---|---|---|---|---|---|
Tissue |
ctDNA to tissue, % |
Tissue to ctDNA, % |
|||||
Positive | Negative | Total | PPA | 87.8 | 81.8 | ||
ctDNA | Positive | 72 | 16 | 88 | PPV | 81.8 | 87.8 |
Negative | 10 | 57 | 67 | NPA | 78.1 | 85.1 | |
Total | 82 | 73 | 155 | NPV | 85.1 | 78.1 | |
OPA | 83.2 | 83.2 |
Secondary analysis population (N = 118)b | |||||||
---|---|---|---|---|---|---|---|
Tissue |
ctDNA to tissue, % |
Tissue to ctDNA, % |
|||||
Positive | Negative | Total | PPA | 89.6 | 85.7 | ||
ctDNA | Positive | 60 | 10 | 70 | PPV | 85.7 | 89.6 |
Negative | 7 | 41 | 48 | NPA | 80.4 | 85.4 | |
Total | 67 | 51 | 118 | NPV | 85.4 | 80.4 | |
OPA | 85.6 | 85.6 |
Biomarkers included are KRAS SNVs, NRAS SNVs, BRAF V600E, MSI-H, and ERBB2 CNVs.
ctDNA, circulating tumor DNA; NPA, negative percent agreement; MSI, microsatellite instability; NPV, negative predictive value; OPA, overall percent agreement; PPA, positive percent agreement; PPV, positive predictive value; SNV, single-nucleotide variant; SOC, standard of care.
Samples that were negative, in which testing failed, which had no detectable tumor, or were not assessed for all biomarkers of interest are classified as ‘negative’.
Secondary analysis population excludes samples in which testing failed, which had no detectable tumor, were not assessed for biomarkers of interest (N = 12), or samples where tissue was taken >20 days prior to stage IV diagnosis (N = 25).