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. 2015 May 25;6(18):16725–16734. doi: 10.18632/oncotarget.4264

Table 1. Characteristics of trials included in the Meta-analysis.

Study ID country Trial phase N(T/C) Male
(T/C,%)
Ages
(T/C,Years)
Interventions outcomes
TKI-group Non-TKI-group ORR OS CNS-TTP PFS Adverse event (grade≥3)
Lee et al. 2014 Britain II 40/40 37.5/52.5 61.3/62.2 erlotinib+WBRT placebo+WBRT N Y Y N Y
Zhuang et al. 2013 China II 23/31 43/42 60/63 erlotinib+WBRT WBRT Y Y Y Y Y
Sperduto et al. 2013 America III 41/44 N 61/64 erlotinib+WBRT/SRS WBRT/SRS N Y Y N Y
Fu et al. 2012 China N 38/123 N N gefitinib+WBRT/SRS WBRT/SRS Y N N N Y
Pesce et al. 2011 Switzerland II 16/43 56/63 57/63 gefitinib+WBRT TMZ+WBRT N Y N N Y
Wang et al. 2014 China N 37/36 67.6/63.9 61/62 gefitinib+3D-CRT VMP+3D-CRT Y Y N N Y
Cai et al. 2014 China N 104/178 59.6/66.3 65/65 TKI+WBRT/SRS/S WBRT/SRS/S N Y Y N N
Fan et al. 2013 China N 75/111 57.3/73.0 57/57 TKI+WBRT/SRS/S chemotherapy+WBRT/SRS/S N Y N N N

Abbreviation: N(T/C): number of patients(test group/control group); ORR: object response rate; OS: overall survival; CNS-TTP: time to central nerves system/neurological progression / neurological progression-free survival/progression-free survival of intracranial disease/local progression-free survival; PFS: progression-free survival; N: no mention in the paper; Y: have mentioned in the paper.