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. 2017 Apr 12;28(8):1713–1729. doi: 10.1093/annonc/mdx175

Table 7.

Trials’ subset and sensitivity analyses for prognostic analysis in the experimental arm for OS, PFS and ORR

Main analysis Trials’ subset analysis
Sensitivity analyses
Type of anti-EGFR
Only phase III (without PEAK) Only first line (without 20050181)
Parameter Cetuximab Panitumumab
OS
HR (95% CI) 2.03 (1.69–2.42) 2.11 (1.68–2.66) 1.90 (1.43–2.53) 1.99 (1.65–2.39) 2.03 (1.67–2.47)
P value <0.001 <0.001 <0.001 <0.001 <0.001
P value for interactiona 0.57
P value for heterogeneity 0.46 0.25 0.44 0.54 0.46
PFS
HR (95% CI) 1.59 (1.34–1.88) 1.77 (1.43–2.20) 1.34 (1.02–1.75) 1.59 (1.33–1.89) 1.63 (1.35–1.96)
P value <0.001 <0.001 0.03 <0.001 <0.001
P value for interactiona 0.11
P value for heterogeneity 0.58 0.73 0.73 0.58 0.65
ORR
OR (95% CI) 0.38 (0.28–0.50) 0.35 (0.25–0.50) 0.42 (0.27–0.66) 0.33 (0.24–0.44) 0.40 (0.30–0.53)
P value <0.001 <0.001 <0.001 <0.001 <0.001
P value for interactiona 0.55
P value for heterogeneity 0.08 0.50 0.02 0.64 0.22
a

Test comparing the HRs between the two trial subsets (cetuximab, panitumumab).

HR, hazard ratio; OR, odds ratio; CI, confidence interval; ORR, objective response rate; OS, overall survival; PFS, progression-free survival.