Table 1.
Parameter | N (%) |
---|---|
Age (median) |
62.6 years |
Gender (Female/Male) |
97 (43.0%)/129 (57.0%) |
Histological Grade |
|
1–2 |
170 (75.2%) |
3-4 |
46 (20.4%) |
Obstruction Yes/No |
30 (13.2%)/179 (79.2%) |
Perforation Yes/No |
9 (4.0%)/201 (89.0%) |
Primary Site Left/Right |
165 (73.0%)/60 (26.6%) |
Rectum |
71 (31.0%) |
TNM stage at biopsy |
|
I-III versus IV |
83 (36.8%)/137 (60.6%) |
Median Follow Up |
73.6 months |
Deaths |
175 (77.4%) |
Line of therapy at Cetuximab administration |
|
1st line |
38 (16.8%) |
2nd line |
108 (47.8%) |
3rd line and beyond |
80 (35.4%) |
Type of therapy at Cetuximab administration |
|
Irinotecan-based |
153 (48.7%) |
Oxaliplatin-based |
84 (26.7%) |
Both irinotecan and oxaliplatin |
29 (9.2%) |
Only fluoropyrimidine |
6 (1.9%) |
Single-agent Cetuximab |
42 (13.4%) |
Objective Response to Cetuximab |
|
All lines of therapy |
|
Complete Respone (CR) |
2 (0.9%) |
Partial Response (PR) |
55 (24.4%) |
ORR (CR+PR) |
57 (25.3%) |
Stable disease (SD) |
66 (29.3%) |
Progressive disease (PD) |
70 (31.1%) |
ORR by line of Cetuximab therapy |
|
1st line |
17 (44.7%) |
2nd line |
23 (21.5%) |
3rd line | 14 (22.9%) |