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. 2026 Jan 30;17:1709044. doi: 10.3389/fphar.2026.1709044

TABLE 2.

Principal characteristics of RCTs included in the meta-analysis.

study (year) Age (years) C Sample size Tumor responses criteria Stage Intervention Cinobufacini dose Duration (cycles) Outcome measures
T (T/C) T C
Zhou, 2023 57.89 ± 6.12 58.47 ± 6.25 43/43 RECIST III,IV XELOX + CC XELOX 0.5g-tid-po 2 ①②⑤
Cheng, 2023 53.42 ± 7.34 52.63 ± 7.21 31/31 NA IIIB,IV FOLFOXIRI + CC FOLFOXIRI 0.5g-tid-po 6 ③④
Song, 2022 61.98 ± 5.77 62.15 ± 5.87 50/50 RECIST III,IV FOLFOX + CC FOLFOX 0.5g-bid-po 4 ①②③④⑤
Zhang, 2021 53.36 ± 7.43 53.41 ± 7.46 36/36 RECIST III,IV XELOX + CC XELOX 0.5g-tid-po 2 ①②⑤
Yang, 2021 58.30 ± 7.89 59.61 ± 7.93 31/31 RECIST III,IV XELOX + CC XELOX 0.5g-tid-po 6 ①②③⑤
Zhong, 2019 62-82 64-78 44/42 RECIST III,IV XELOX + CC XELOX 0.75g-tid-po 2 ①②⑤
Sha, 2018 42-70 43-72 41/41 NA III,IV PTX + OX + CC PTX + OX 0.5g-tid-po 2 ③④
Dong, 2017 58. 6 ± 7. 4 60.2 ± 6.8 38/38 Unclear III,IV XELOX + CC XELOX 0.5g-tid-po 4 ①②⑤
Shi, 2017 35. 57 ± 2. 35 35.42 ± 4. 8 34/34 RECIST III FOLFOX + CC FOLFOX 0.6g-bid-po 4 ①②⑤
Lu, 2014 38–75 36–73 30/30 RECIST III,IV FOLFOX + CC FOLFOX 0.5g-tid-po 2 ①②⑤
Wang, 2023 58.14 ± 7.31 57.89 ± 7.03 40/40 WHO IIIB,IV XELOX + CC XELOX 0.5g-tid-po 4 ①②③④
Fang, 2021 68.72 ± 3.21 68.80 ± 3.19 60/60 RECIST IIIB,IV XELOX + CC XELOX 0.5g-tid-po 4 ①②③

C: control group, T: treatment group, NA: not available, RECIST: response evaluation criteria in solid tumors, WHO:World Health Organization XELOX: Xeloda + Oxaliplatin, FOLFOXIRI: Leucovorin+5-Fluorouracil + Oxaliplatin + Irinotecan, FOLFOX: Leucovorin+5-Fluorouracil + Oxaliplatin, PTX + OX: Raltitrexed + Oxaliplatin, CC: cinobufacini capsule, Outcome measures: ①: DCR, ②: ORR, ③: Tumor Markers, ④: CD4 T cells, ⑤: Adverse Events.