Table 3.
Characteristic | Treatment group | Hazard ratio (95% CI) | P |
---|---|---|---|
Lowest BMD T-score | .04a | ||
≤ -2.0 | Placebo | 1.00 | |
Letrozole | 0.67 (0.52 to 0.86) | ||
> -2.0 | Placebo | 1.00 | |
Letrozole | 0.91 (0.79 to 1.06) | ||
Age, y | <.001 | ||
Younger than 60 | 1.00 | ||
60 and older | 1.67 (1.44 to 1.95) | ||
Pathologic nodal status | <.001 | ||
Negative | 1.00 | ||
Positive | 1.38 (1.21 to 1.57) | ||
Received tamoxifen | <.001 | ||
No | 1.00 | ||
Yes | 0.76 (0.66 to 0.87) |
P interaction between treatment and T-score (for placebo, lowest T-score above -2.0 compared with no more than -2.0: HR = 0.74, 95% CI = 0.61 to 0.90; for letrozole lowest T-score: above -2.0 compared with no more than -2.0: HR = 1.01, 95% CI = 0.81 to 1.26). BMD = bone mineral density; DFS = disease-free survival; NSABP = National Surgical Adjuvant Breast and Bowel Project.