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. 2018 Apr 6;18:396. doi: 10.1186/s12885-018-4303-z

Table 4.

Adverse Events

Total N(%) Grade
1 2 3–4
Apatinib alonea 45 (100%)
Fatigue 8(17.8%) 5 2 1
Hypertension 35(77.8%) 27 3 5
Proteinuria 4(8.9%) 3 1
Hand-foot syndrome 12(26.7%) 10 2
Diarrhea 9(20%) 5 3 1
Weight loss 19(42.2%) 17 2
Hair hypopigmentation 25(55.6%) 20 5
Anorexia 17(37.8%) 10 4 3
Rash or desquamation 26(57.8%) 15 9 2
Mucositis 2(4.4%) 2
Pneumothorax 9(20%) 3 6
Wound-healing problems 6(13.3%) 1 5
Elevated Aminotransferase or bilirubin 3(6.7%) 2 1
Thrombocytopenia 7(15.6%) 5 1 1
Seizure-like attack 1(2.3%) 1
Pancreatitis 1(2.2%) 1
Anemia 2(4.4%) 2
Cranial neuritis 1(2.3%) 1
Apatinib + everolimusb 7 (100%)
Mucositis 7(100%) 2 4 1
Hypertension 4(57.1%) 2 2
Rash or desquamation 5(71.4%) 2 3
Gastrointestinal uncomfort 1(14.3%) 1
Apatinib + GTc 5 (100%)
Hypertension 1(20%) 1
Rash or desquamation 2(40%) 2
Wound-healing problems 1(20%) 1
Thrombocytopenia 2(40%) 1 1

aApatinib alone: apatinib 500-750 mg/d according to the patient’s weight

bApatinib + everolimus: apatinib 250–500 mg/d + everolimus 5 mg/d according to the patient’s weight

cGT chemo-protocol combined with gemcitabine 1000 mg/m2 d1,8 and docetaxel 75 mg/m2 d8 once every 21 days