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.