A next-generation sequencing (NGS) report helps you understand the genomic information about your cancer.

Typically, on the first or second page of the NGS report you will see a list of genes in “Genomic Findings” or “Genomic Variants” or “Molecular Findings”. On this list, you may see genes with “amplification” or “copy number gain”. 

If your report includes CCNE1, MYC, KRAS, or other genes with amplification or copy number gain, you may be eligible for the study.