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. 2020 Mar 6;10:313. doi: 10.3389/fonc.2020.00313

Table 4.

Subgroup analysis for progression-free survival, overall survival, and objective response rate.

Group PFS OS ORR
No. of studies HR (95% CI) P I2 (%) No. of studies HR (95% CI) P I2 (%) No. of studies RR (95% CI) P I2 (%)
Total 8 0.81 [0.66, 0.99] 0.04 0 6 1.00 [0.95, 1.05] 0.97 0 5 0.91 [0.64, 1.29] 0.58 20
Nation
East Asia 5 0.75 [0.58, 0.98] 0.03 20 3 1.02 [0.69, 1.50] 0.93 0 4 0.92 [0.63, 1.34] 0.65 39
Egypt 1 0.96 [0.51, 1.82] 0.90 NA 1 1.00 [0.87, 1.15] 1 NA 1 0.83 [0.30, 2.31] 0.73 NA
Canada 1 0.84 [0.41, 1.74] 0.64 NA 1 0.63 [0.26, 1.50] 0.3 NA NA NA NA NA
Italy 1 0.89 [0.57, 1.40] 0.61 NA 1 1.09 [0.44, 2.68] 0.85 NA NA NA NA NA
Treatment line
First line 4 0.76 [0.58, 1.00] 0.05 0.37 3 0.96 [0.61, 1.51] 0.87 0 2 0.57 [0.31, 1.02] 0.06 0
First and second line 1 0.84 [0.41, 1.74] 0.64 NA 1 0.63 [0.26, 1.50] 0.30 NA NA NA NA NA
Unclear 3 0.87 [0.63, 1.22] 0.43 0 2 1.00 [0.95, 1.05] 0.97 0 3 1.20 [0.77, 1.89] 0.42 0
Initial dosage
50 mg/d 5 0.76 [0.59, 0.97] 0.03 0 4 1.00 [0.95, 1.05] 0.99 0 3 1.20 [0.77, 1.89] 0.42 0
50/37.5/25 mg/d 1 0.54 [0.21, 1.38] 0.20 NA NA NA NA NA 1 0.62 [0.30, 1.25] 0.18 NA
Unclear 2 0.99 [0.68, 1.43] 0.94 0 2 0.93 [0.54, 1.63] 0.81 0 1 0.50 [0.18, 1.40] 0.19 NA
Study qualitya
High quality 5 0.80 [0.64, 1.01] 0.06 16 4 1.03 [0.72, 1.47] 0.87 0 3 1.05 [0.67, 1.64] 0.83 35
Medium quality 3 0.81 [0.53, 1.25] 0.35 0 2 1.00 [0.95, 1.05] 0.95 7 2 0.69 [0.38, 1.24] 0.21 0
Study design
RCT 1 0.75 [0.44, 1.27] 0.29 NA 1 1.15 [0.64, 2.05] 0.64 NA 1 1.42 [0.80, 2.51] 0.23 NA
RS 7 0.82 [0.65, 1.02] 0.07 0 5 1.00 [0.95, 1.05] 0.94 0 4 0.71 [0.45, 1.12] 0.14 0

PFS, progression-free survival; OS, overall survival; ORR, objective response rate; HR, hazard ratio; RR, risk ratio; CI, confidence interval; NA, not available.

a

Study quality was evaluated using the Newcastle-Ottawa Scale for retrospective observational studies and the Jadad scale for randomized controlled trials.