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. 2021 Aug 21;2021:5596415. doi: 10.1155/2021/5596415

Table 1.

Principal characteristics of the studies included in the meta-analysis.

Study ID Sample size(T/C)/case Age (mean ± SD) Stage Intervention Cinobufacini dose Duration(day) Outcome
Test group Control group Test group Control group
Su [22] 44/44 56.48 ± 7.05 55.74 ± 6.12 IIIb, IV DP + cinobufacini DP 0.6 g·bid·po 84 ①④⑤⑥
Li [23] 21/18 —— —— IIIb, IV DP + cinobufacini DP 0.75 g·tid·po 90
Chen et al. [24] 36/31 54.26 ± 10.38 53.45 ± 11.69 III, IV GP + cinobufacini GP 0.5 g·tid·po 84 ①②③④⑤⑥⑦
Li [25] 38/37 60.09 ± 4.81 58.97 ± 4.63 III, IV DP + cinobufacini DP 0.5 g·tid·po 42 ①⑥⑦
Huang [26] 43/43 61.58 ± 7.26 61.23 ± 7.15 IIIb, IV GP + cinobufacini GP 0.5 g·bid·po 42 ①⑥⑦
Li et al. [23] 58/58 56.38 ± 8.24 57.12 ± 8.44 IIIb, IV GP + cinobufacini GP 0.5 g·bid·po 84 ①③⑥⑦
Lan et al. [27] 43/42 55.63 ± 12.05 56.49 ± 11.61 III, IV TC + cinobufacini TC 0.5 g·tid·po 63
Chen et al. [28] 31/31 55.87 ± 6.58 56.29 ± 6.49 IIIb, IV GP/AP + cinobufacini GP/AP 0.5 g·tid·po 42 ①⑤⑥⑦
Yu et al. [29] 33/30 —— —— III, IV GP + cinobufacini GP 0.5 g·tid·po 42 ①④⑤⑥
Liu [30] 40/40 67.88 ± 2.27 68.54 ± 2.11 IIIb, IV TP/NP + cinobufacini TP/NP 0.6 g·bid·po 42 ②④⑤⑥
Chen et al. [31] 36/36 56.90 ± 11.00 56.20 ± 10.70 IIIb, IV TC + cinobufacini TC 0.5 g·tid·po 84 ①⑦
Pu et al. [32] 42/38 54.60 ± 9.38 57.83 ± 12.42 III, IV GP + cinobufacini GP 0.5 g·bid·po 42 ①②③⑥⑦
Shi [33] 51/51 —— —— III, IV TP + cinobufacini TP 0.6 g·tid·po 42 ①②④⑤⑥
Wei and Xu [34] 34/34 57.39 ± 4.31 58.31 ± 2.57 III, IV GP + cinobufacini GP 0.5 g·tid·po 42 ①④⑥
Chen et al. [35] 40/40 59.30 ± 7.90 59.50 ± 7.50 IIIb, IV GP + cinobufacini GP 0.6 g·tid·po 42 ①②③
Li et al. [36] 63/63 58.73 ± 9.54 57.96 ± 9.86 IIIb, IV DP + cinobufacini DP 0.5 g·tid·po 105 ①②③④⑤⑥
Xiao et al. [37] 68/62 —— —— IV GP + cinobufacini GP 0.5 g·tid·po 42
Liu [38] 45/40 —— —— III, IV NP/TP + cinobufacini NP/TP 0.5 g·bid·po 42 ①②③④⑤⑥
Miao et al. [39] 30/30 58.00 ± 7.00 57.00 ± 6.50 IIIb, IV TP + cinobufacini TP 0.5 g·tid·po 84 ①④⑥

Note. (1) T is the test group; C is the control group; AP: pemetrexed + cisplatin; DP: docetaxel + cisplatin; GP: gemcitabine + cisplatin; NP: vinorelbine + cisplatin; TC: paclitaxel + carboplatin; TP: paclitaxel + cisplatin; (2) outcome index: ① ORR; ② one-year survival rate; ③ two-year survival rate; ④ leukocyte toxicity; ⑤ platelet toxicity; ⑥ vomiting reaction; ⑦ immune response.