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. 2020 Dec 21;10(2):615–625. doi: 10.1002/cam4.3638

TABLE 1.

Patient demographics and clinical characteristics.

Characteristics

Total (N = 289)

No. of patients (%)

FOLFIRI + Bevacizumab (N = 119) FOLFIRI + Ramucirumab (N = 107) FOLFIRI + Aflibercept (N = 63) p value
Age at enrollment, years
Median [range] 63.0 [31.0–84.0] 63.0 [32.0–82.0] 64.0 [31–84.0] 62.0 [43.0–80.0] 0.87
Sex
Male 137 (47.4) 57 (47.9) 46 (43.0) 34 (54.0) 0.39
Female 152 (52.6) 62 (52.1) 61 (57.0) 29 (46.0)
Primary site
Right‐sided colon 93 (32.2) 39 (32.8) 22 (20.6) 17 (27.0) 0.12
Left‐sided colon 196 (67.8) 80 (67.2) 85 (79.4) 46 (73.0)
Metastatic site
Liver 148 (51.2) 58 (48.7) 59 (55.1) 31 (49.2) 0.59
Lung 145 (50.2) 66 (55.5) 49 (45.8) 36 (57.1) 0.25
Peritoneal 97 (33.6) 38 (31.9) 31 (29.0) 25 (39.7) 0.34
Lymph node 99 (34.3) 40 (33.6) 40 (37.4) 17 (27.0) 0.38
Other 41 (14.2) 14 (11.8) 16 (15.0) 11 (17.5) 0.54
RAS status in tissue
Wild type 134 (46.4) 47 (39.5) 57 (53.3) 30 (47.6) 0.11
Mutant 155 (53.6) 72 (60.5) 50 (46.7) 33 (52.4)
Prior bevacizumab exposure in first‐line chemotherapy
Yes 159 (55.0) 68 (57.1) 54 (50.5) 37 (58.7) 0.55
No 130 (45.0) 51 (42.9) 53 (49.5) 26 (41.3)
First‐line progression‐free survival (Patients treated with Bevacizumab only)
≤9 months 71 (44.7) 25 (36.8) 29 (53.7) 17 (45.9) 0.16
>9 months 88 (55.3) 43 (63.2) 25 (46.3) 20 (54.1)
Patients who experienced relapse within 6 months of completing oxaliplatin‐based adjuvant therapy
Yes 40 (13.8) 15 (12.6) 15 (14.0) 10 (15.9) 0.84
No 249 (86.2) 104 (87.4) 92 (86.0) 53 (84.1)
Tumor markers (at initiation of second‐line chemotherapy)
CEA median, [range] 17.3 [0.5–17056.1] 16.8 [1.0–1501.4] 28.3 [0.5–17056.1] 14.9 [1.0–7415] 0.30
CA19‐9 median, [range] 32.7 [2.0–50000] 27.6 [2.0–29210.2] 33.0 [2.0–50000] 33.6 [2.0–50000] 0.71
RAS:rat sarcoma viral oncogene homolog
CEA: carcinoembryonic antigen
CA19‐9: carbohydrate antigen 19–9