Table 1.
Patient characteristics and clinical use
n | % | |
---|---|---|
(A) Patient characteristics | ||
Sex | ||
Male | 1234 | 61.5 |
Female | 772 | 38.5 |
Age | ||
<65 years | 1032 | 51.4 |
≥65 years | 971 | 48.4 |
Unknown | 3 | 0.2 |
Tumour site (including overlapping sites) | ||
Colon | 1235 | 61.6 |
Rectum | 775 | 38.6 |
PS | ||
0 | 1370 | 68.3 |
1 | 630 | 31.4 |
2 | 2 | 0.1 |
Unknown | 4 | 0.2 |
Treatment line | ||
Second line | 133 | 6.6 |
Third line and later treatment | 1869 | 93.2 |
Others | 4 | 0.2 |
Previous chemotherapy | ||
(−) | 3 | 0.2 |
(+) | 2003 | 99.9 |
FOLFIRI | 1510 | 75.3 |
FOLFOX | 1854 | 92.4 |
5-FU/LV | 370 | 18.4 |
Irinotecan | 261 | 13.0 |
UFT/LV | 337 | 16.8 |
Bevacizumab | 923 | 46.0 |
Previous surgery | ||
(−) | 81 | 4.0 |
(+) | 1925 | 96.0 |
Previous radiation therapy | ||
(−) | 1650 | 82.3 |
(+) | 355 | 17.7 |
Unknown | 1 | 0.0 |
EGFR-IHC | ||
Positive | 1974 | 98.4 |
Negative | 29 | 1.4 |
Not tested | 3 | 0.2 |
KRAS status | ||
Wild | 249 | 12.4 |
Mutant | 53 | 2.6 |
Not tested | 1691 | 84.3 |
Unknown | 13 | 0.7 |
Comorbidity | ||
(−) | 1019 | 50.8 |
(+) | 974 | 48.6 |
Unknown | 13 | 0.6 |
(B) Clinical use | ||
No. of treatments | ||
<4 | 253 | 12.6 |
4 to <16 | 900 | 44.9 |
16 to <32 | 524 | 26.1 |
32 to <48 | 255 | 12.7 |
≥48 | 74 | 3.7 |
Duration of treatment | ||
<4 weeks | 276 | 13.8 |
4 to < 16 weeks | 739 | 36.8 |
16 to <32 weeks | 489 | 24.4 |
32 to <48 weeks | 280 | 14.0 |
≥48 weeks | 222 | 11.1 |
Cumulative dose | ||
<1500 mg/m2 | 435 | 21.7 |
1500 to <3000 mg/m2 | 493 | 24.6 |
3000 to < 9000 mg/m2 | 832 | 41.5 |
≥9000 mg/m2 | 236 | 11.8 |
Unknown | 10 | 0.5 |
Combination chemotherapy | ||
(−) | 460 | 22.9 |
(+) | 1546 | 77.1 |
Irinotecan | 1255 | 62.6 |
FOLFIRI | 256 | 12.8 |
Others | 35 | 1.7 |
Combination radiation therapy | ||
(−) | 1943 | 96.9 |
(+) | 59 | 2.9 |
Unknown | 4 | 0.2 |
Pre-medicationa | ||
No | 14 | 0.7 |
Antihistamine alone | 185 | 9.2 |
Corticosteroid alone | 23 | 1.2 |
Antihistamine + corticosteroid | 1783 | 88.9 |
PS, performance status; 5-FU, 5-fluorouracil; LV, leucovorin; UFT, tegafur-uracil; EGFR, epidermal growth factor receptor; IHC, immunohistochemistry.
aExcluded unknown (one patient).