Table 1.
Characteristic | |
---|---|
| |
Mean age (SD), years | 54 (12) |
| |
Sex | |
Male | 168 (60.9) |
Female | 108 (39.1) |
| |
Ethnicity | |
Caucasian | 236 (85.5) |
African American | 15 (5.4) |
Asian | 20 (7.2) |
Other | 5 (1.8) |
| |
Median BMI (IQR) | 27.0 (7.2) |
| |
ASA score | |
I | 0 |
II | 63 (22.8) |
III | 210 (76.1) |
IV | 3 (1.1) |
| |
Previous abdominal surgery | 63 (22.8) |
| |
Pre-treatment AJCC staging | |
I | 42 (15.2) |
II | 34 (12.3) |
III | 176 (63.8) |
IV | 24 (8.7) |
| |
Clinical T stage (cT) | |
T0 / Tis | 9 (3.3) |
T1 | 13 (5.7) |
T2 | 43 (15.6) |
T3 | 185 (67.0) |
T4 | 26 (9.5) |
| |
Clinical N stage (cN) | |
N0 | 86 (31.2) |
N1 | 137 (49.6) |
N2 | 53 (19.2) |
| |
Clinical M stage (cM) | |
M0 | 252 (91.3) |
M1 | 24 (8.7) |
| |
Neo-adjuvant treatment | |
Long course chemo-radiotherapy | 171 (61.9) |
Short course radiotherapy | 1 (0.4) |
Induction chemotherapy, followed by radiotherapy | 14 (5.1) |
Chemotherapy only | 20 (7.2) |
Did not receive neo-adjuvant treatment | 70 (25.4) |
| |
Adjuvant treatment | |
FOLFOX / CAPOX | 125 (45.3) |
Fluorouracil / Capecitabine only | 76 (27.5) |
FOLFOX + Bevacizumab | 12 (4.3) |
FOLFIRI + Bevacizumab | 8 (2.9) |
Other | 5 (1.8) |
Did not receive chemotherapy | 50 (18.9) |
| |
Median time to adjuvant treatment (IQR), days | 42 (21) |
Data are number of patients (%) unless otherwise indicated.
Abbreviations: SD, Standard Deviation; BMI, body mass index; IQR, Inter-quartile range; ASA, American Society of Anesthesiologists; AJCC, American Joint Committee on Cancer; FOLFOX, Folinic acid + Fluorouracil + Oxaliplatin; CAPOX: Capecitabine + Oxaliplatin; FOLFIRI: Folinic acid + Fluorouracil + Irinotecan.