Skip to main content
. 2016 Oct;5(5):511–516. doi: 10.21037/tlcr.2016.10.14

Table 1. Survival data according to KRAS status in blood.

Author, year Study population (n) NSCLC Stage Therapeutic regimen Specimen type PFS (months) P value (PFS) OS (months) P value (OS)
Camps C. et al., (30) 2005 67 IIIB or IV Chemotherapy Serum KRAS +: 7.3 0.2300 KRAS +: 11.4 0.2800
WT: 5.5 WT: 12.5
Gautschi O. et al., (31) 2007 175 I, II, III (A/B) or IV Surgery + chemotherapy Plasma Worse OS of patients with mutant plasma KRAS 0.0370
Wang S. et al., (32) 2010 120 IIIB or IV EGFR-TKI Plasma KRAS+: 2.5 <0.0010 KRAS +: 16.9 0.8270
WT: 8.8 WT: 20.3
Nygaard AD. et al., (33) 2013 246 III or IV Chemotherapy Plasma KRAS +: 3.0 0.0043 KRAS +: 4.8 0.0002
WT: 5.6 WT: 9.5
Kim ST. et al., (34) 2013 57 IIIB and IV EGFR-TKI Serum KRAS +: 3.9 0.4520
WT: 10.4
Nygaard AD. et al., (35) 2014 69 III or IV Chemotherapy Plasma KRAS +: 2.1 0.0100 KRAS +: 3.6 0.0300
WT: 5.5 WT: 8.4
Ai B. et al.,(16) 2016 meta-analysis (30,31,33,35) III or IV Chemotherapy cfDNA No significant differences 0.4500 No significant differences 0.8900

NSCLC, non-small cell lung cancer; PFS, progression-free survival; OS, overall survival; EGFR, epidermal growth factor receptor; cfDNA, circulating free DNA.