Table 1:
Placebo (n=1983) | Letrozole (n=1983) | |||
---|---|---|---|---|
Characteristic | n | % | n | % |
Age at randomization, yrs | ||||
<60 | 675 | 34.0 | 685 | 34.5 |
≥60 | 1308 | 66.0 | 1298 | 65.5 |
Race | ||||
White | 1840 | 92.8 | 1848 | 93.2 |
Black | 81 | 4.1 | 70 | 3.5 |
Asian | 39 | 2.0 | 39 | 2.0 |
Other/Unknown | 23 | 1.2 | 26 | 1.3 |
Pathologic Nodal Status | ||||
Negative | 1134 | 57.2 | 1145 | 57.7 |
Positive | 849 | 42.8 | 838 | 42.3 |
Lowest BMD T-score | ||||
≤−2.0 | 493 | 24.9 | 489 | 24.7 |
>−2.0 | 1490 | 75.1 | 1494 | 75.3 |
Duration of Tamoxifen Prior to Randomization, mos | ||||
0 | 1212 | 61.1 | 1207 | 60.9 |
1 to 12 | 164 | 8.3 | 150 | 7.6 |
13 to 24 | 254 | 12.8 | 259 | 13.1 |
25 to 36 | 353 | 17.8 | 367 | 18.5 |
Surgery Type | ||||
Lumpectomy | 1208 | 60.9 | 1201 | 60.6 |
Mastectomy | 775 | 39.1 | 782 | 39.4 |
HER 2 Status | ||||
Positive | 278 | 14.0 | 287 | 14.5 |
Negative | 1547 | 78.0 | 1546 | 78.0 |
Not done/Unknown | 158 | 8.0 | 150 | 7.6 |
Duration of AI prior to randomization, mos* | ||||
≤36 | 412 | 20.8 | 399 | 20.1 |
37 to 48 | 192 | 9.7 | 207 | 10.4 |
49 to 60 | 992 | 50.0 | 970 | 48.9 |
>60 | 387 | 19.5 | 407 | 20.5 |
Duration of AI for one patient in placebo group was unknown, presented in the “≤36” category.