Table 1 Relationship between the eligibility criteria and clinicopathological features (n = 160).

From: Prognostic impact of clinical trial eligibility in patients with advanced gastric cancer

Factor

 

Eligibility criteria, n (%)

P value

Total

(n = 160)

Eligible group

(n = 76)

Ineligible group

(n = 84)

 

Sex, male/female

98 (61.3)/62 (38.8)

50 (65.8)/26 (34.2)

48 (57.1)/36 (42.9)

0.33

Median age, years

68

63

72

< 0.01

Performance status, 0–1/2–3

116 (72.5)/44 (27.5)

76 (100.0)/0 (0.0)

40 (47.6)/44 (52.4)

< 0.01

Tumor location, whole–upper/middle–lower

96 (60.0)/64 (40.0)

46 (60.5)/30 (39.5)

50 (59.5)/34 (40.5)

1.00

Macroscopic type, type non–4/type 4

100 (62.5)/60 (37.5)

47 (61.8)/29 (38.2)

53 (63.1)/31 (36.9)

0.87

Depth of tumor invasion, cT1–2/cT3–4

1 (0.6)/159 (99.4)

1 (1.3)/75 (98.7)

0 (0.0)/84 (100.0)

0.48

Lymph node metastasis, cN0–1/cN2–3

61 (38.1)/99 (61.9)

29 (38.2)/47 (61.8)

32 (38.1)/52 (61.9)

1.00

Number of distant metastatic sites, 1/ 2

116 (72.5)/44 (27.5)

54 (71.1)/22 (29.0)

62 (73.8)/22 (26.2)

0.73

Liver metastasis, presence

34 (21.3)

18 (23.7)

16 (19.1)

0.56

Lung metastasis, presence

3 (1.9)

3 (4.0)

0 (0.0)

0.10

Distant lymph node metastasis, presence

46 (28.8)

24 (31.6)

22 (26.2)

0.49

Peritoneal dissemination, presence

107 (66.9)

46 (60.5)

61 (72.6)

0.13

Bone metastasis, presence

4 (2.5)

0 (0.0)

4 (4.8)

0.12

Histological type, differentiated/undifferentiated

36 (22.5)/124 (77.5)

17 (22.4)/59 (77.6)

19 (22.6)/65 (77.4)

1.00

First-line regimen of chemotherapy, S-1 alone/taxane-based or platinum-based

3 (1.9)/157 (98.1)

0 (0.0)/76 (100.0)

3 (3.6)/81 (96.4)

0.25

Dose reduction in the first-line chemotherapy initiation, presence

60 (37.5)

22 (28.9)

38 (45.2)

0.04

Median number of administrations in the first-line chemotherapy

4

5

3

< 0.01

Treatment-related adverse events (any grade), presence

142 (88.8)

67 (88.2)

75 (89.3)

1.00

Conversion surgery, presence

44 (27.5)

29 (38.2)

15 (17.9)

< 0.01