Skip to main content
. 2017 Sep 5;10:153. doi: 10.1186/s13045-017-0521-0

Table 1.

Characteristics of 269 apatinib-treated gastric cancer patients from two clinical trials included in the present study

Without adverse eventsa
No. (%)
With adverse events
No. (%)
P valueb
Overall 119 (44.24) 150 (55.76)
Trial
 Phase II 45 (37.82) 48 (32.00) 0.319
 Phase III 74 (62.18) 102 (68.00)
Age (years)
 < 30 2 (1.68) 1 (0.67) 0.319
 30–39 10 (8.40) 8 (5.33)
 40–49 23 (19.33) 26 (17.33)
 50–59 53 (44.54) 60 (40.00)
 60–69 29 (24.37) 54 (36.00)
 ≥ 70 2 (1.68) 1 (0.67)
Sex
 Female 27 (22.69) 37 (24.67) 0.705
 Male 92 (77.31) 113 (75.33)
ECOG PS
 0 21 (17.65) 32 (21.33) 0.450
 1 98 (82.35) 118 (78.67)
Stage at diagnosis
 II 2 (1.68) 1 (0.67) 0.755
 III 7 (5.88) 6 (4.00)
 IV 109 (91.60) 141 (94.00)
Pathological grading
 Gx 12 (10.53) 21 (15.11) 0.280
 G1 6 (5.26) 4 (2.88)
 G2 46 (40.35) 44 (31.65)
 G3 50 (43.86) 70 (50.36)
No. of metastatic sites
 ≤ 2 79 (66.39) 104 (69.80) 0.551
 > 2 40 (33.61) 45 (30.20)
Prior surgery of primary tumor
 Yes 86 (72.27) 108 (72.00) 0.961
 No 33 (27.73) 42 (28.00)
Prior radiotherapy
 Yes 19 (15.97) 21 (14.00) 0.653
 No 100 (84.03) 129 (86.00)
Neoadjuvant chemotherapy
 Yes 32 (26.89) 45 (30.00) 0.575
 No 81 (73.11) 105 (70.00)
Months since diagnosisc 15.7 (10.1–29.9) 18.3 (11.8–31.4) 0.1876
Comorbidity
 Yes 29 (24.37) 44 (29.33) 0.363
 No 90 (75.63) 106 (70.67)
Days since last chemotherapyc 44 (34–91) 46 (32–91) 0.7310
Tumor size
 ≥ 5 cm 50 (42.02) 56 (37.33) 0.435
 < 5 cm 69 (57.98) 94 (62.67)

aAdverse events are defined as hypertension, proteinuria, or hand and foot syndrome in the first 4 weeks of treatment

b P values were calculated from chi-square or Fisher’s exact test for categorical variables, t test for normally distributed continuous variables, and Wilcoxon rank sum test for continuous and skewed variables

cPresented as median (interquartile range) ECOG PS: Eastern Cooperative Oncology Group performance status