Table 1.
Study | Year | Tumor type | N | M/F ratio | Region | Participants
|
Line of apatinib | Outcome index | |
---|---|---|---|---|---|---|---|---|---|
Control | Treatment | ||||||||
Li et al11 | 2013 | Gastric cancer | 144 | 109:33 | China | Placebo | Apatinib (850 mg qd or 425 mg bid) | Third line | ORR, DCR, PFS and OS, adverse reaction |
Li et al16 | 2017 | Hepatocellular carcinoma | 40 | – | China | TACE | Oral apatinib (unknown dose) | Unknown | CR, PR, SD, PD, survival rate of half year/1 year, total survival rate, VEGF and MMP-9 level, adverse reaction |
Lu et al15 | 2017 | Hepatocellular carcinoma | 44 | 33:9 | China | TACE | Oral apatinib (500 mg qd) + TACE | Unknown | AFP level, ORR, PFS, adverse reaction |
Guo and Jing14 | 2017 | Nonsquamous non-small-cell lung cancer | 39 | 20:19 | China | Received chemotherapy | Oral apatinib (500 mg qd) + docetaxel | Second line | PFS, DCR, ORR, adverse reaction |
Wang et al13 | 2017 | Nonsquamous non-small-cell lung cancer | 128 | 87:41 | China | Received chemotherapy | Apatinib + chemotherapy (unknown dose) | Second line | PFS, OS, CR, PR, SD, PD, adverse reaction |
Zhang et al12 | 2012 | Nonsquamous non-small-cell lung cancer | 135 | – | China | Placebo | Apatinib (750 mg qd) | Third line | CR, PR, SD, PD, PFS, adverse reaction |
Li et al17 | 2016 | Gastric cancer | 273 | 201:66 | China | Placebo | Apatinib (850 mg qd) | Third line | CR, PR, SD, PD, OS, PFS, adverse reaction |
Abbreviations: ORR, objective response rate; DCR, disease control rate; PFS, progression-free survival; OS, overall survival; CR, complete remission; PR, partial remission; SD, stable disease; PD, progression disease; AFP, alpha fetoprotein.