Skip to main content
. 2016 Dec 15;3(7):996–998. doi: 10.1001/jamaoncol.2016.4983

Table. Clinical Characteristics, Numbers of Genetic Alterations and Drugs Mentioned in F1 and G360 Reports, and Concordance Between Reports From F1 and G360 Testing.

Patient Characteristic All Mutations Reported by at Least 1 Platform
(n = 112)
Mutations Detectable by Both Platforms
(n = 45)
Drugs Recommended by at Least 1 Platform
(n = 36)
Patient No./Sex Tumor Type Stage Time Difference, mo F1 or G360, No. Both, No. (%) F1, No. Both,
No. (%)
F1, No. G360, No. F1 or G360, No. F1 and G360,
No. (%)
F1, No. G360, No.
1/F Breast cancer IV 0.5 13 7 (54) 6 1/7 (14) 1 5 2 0 2 0
2/F Pancreatic cancer IV 1 16 4 (25) 12 1/4 (25) 3 0 2 0 2 0
3/F Breast cancer IV 15 8 5 (63) 3 0 2 3 2 0 0 2
4/F Thymic carcinoma I 0.5 0 0 0 0 0 0 0 0 0 0
5/F Breast cancer IV 0 9 5 (56) 4 2/5 (40) 1 2 7 4/7 (57) 2 1
6/F Breast cancer IV 0.5 19 4 (21) 15 0 2 2 3 0 2 1
7/M Lung cancer IV 1 18 7 (39) 11 1/7 (14) 1 5 11 1/11 (9) 1 9a
8/M Salivary gland cancer IV 2.5 10 2 (20) 8 2 (100) 0 0 2 0 2 0
9/F Breast cancer III 0 19 11 (58) 8 3/11 (27) 3 5 7 4/7 (57) 0 3
Total 112 45 (40) 67b 10/45 (22) 13 22 36 9/36 (25) 11 16

Abbreviations: F1, FoundationOne; G360, Guardant360.

a

A recommendation of other KIT proto-oncogene receptor tyrosine kinase inhibitors was counted as a single drug.

b

The 67 alterations detectable owing to technical differences only by F1 testing were excluded from the analysis to avoid an exaggerated portrayal of discordance.