Skip to main content
. 2021 Jan 1;26(3):443–449. doi: 10.1007/s10147-020-01844-1

Table 1.

Clinical information and the CGP results of simulated cases

Case 1 Case 2
Gender Male Female
Age 50s 40s
Tumor type Colon cancer Breast cancer (ER+, PgR+, HER2 1+)
Previous chemotherapies
 1st line FOLFOX + bevacizumab Anastrozol
 2nd line FOLFIRI + cetuximab Fulvestrant + palbociclib
 3rd line Investigational drug Paclitaxel + bevacizumab
 4th line Regorafeinib Eriblin
 5th line Capecitabin
 6th line Doxorubicin + cyclophosphamide
Family history of cancer Mother: breast cancer (40s) N/A
Sister: breast cancer (50s)
Medical history Hypertension N/A
Type of GCP test OncoGuide™ NCC oncopanel FoundationOne® CDx
Detected SNVs and CNVs Somatic variants
BRAF V600E PIK3CA H1047R
ATM R35* ERBB2 S310Y
NF1 Y1521* CCND1 amplification
TP53 R273H
APC c.1312+1G>A
ARAF R326*
NTRK2 L138P
Germline variant
BRCA2 V208G

N/A not applicable, CGP comprehensive genomic profiling, SNV single-nucleotide variant, CNV copy number variant, FOLFOX oxaliplatin, folinic acid and 5-fluorouracil, FOLFIRI irinotecan, folinic acid and 5-fluorouracil, BRAF V-Raf murine sarcoma viral oncogene homolog B1, ATM ataxia telangiectasia mutated, NF1 neurofibromatosis type I, TP53 tumor protein p53, APC adenomatous polyposis coli, ARAF V-Raf murine sarcoma 3611 viral oncogene homolog 1, NTRK2 neurotrophic tyrosine receptor kinase 2, BRCA2 breast cancer susceptibility gene 2, PIK3CA phosphoinositide-3-kinase, catalytic, alpha polypeptide, ERBB2 human epidermal growth factor receptor 2, CCND1 cyclin D1