TABLE 2.
Group | Mean % change from baseline to 12 months (95% confidence intervals) |
p-values* | ||
---|---|---|---|---|
N | ||||
LDL-cholesterol | Anastrozole (PAPL) | 54 | −2.3 (−7.64, 3.13) | 0.2859 |
Anastrozole (LITTP) | 94 | −5.4 (−9.31, −1.54) | 0.0007 | |
Anastrozole + risedronate (SP) |
59 | −2.9 (−7.20, 1.38) | 0.0770 | |
HDL-cholesterol | Anastrozole (PAPL) | 54 | 6.9 (2.79, 10.91) | 0.0016 |
Anastrozole (LITTP) | 95 | 6.8 (4.02, 9.49) | < 0.0001 | |
Anastrozole + risedronate (SP) |
60 | 4.0 (0.21, 7.79) | 0.1070 | |
Total cholesterol | Anastrozole (PAPL) | 54 | 0.8 (−3.08, 4.60) | 0.8647 |
Anastrozole (LITTP) | 95 | −2.2 (−4.96, 0.67) | 0.0351 | |
Anastrozole + risedronate (SP) |
60 | −0.4 (−3.27, 2.39) | 0.4840 | |
Triglycerides | Anastrozole (PAPL) | 54 | −0.6 (−7.15, 5.94) | 0.9881 |
Anastrozole (LITTP) | 95 | −0.7 (−5.84, 4.50) | 0.4133 | |
Anastrozole + risedronate (SP) |
60 | 7.0 (−5.02, 19.09) | 0.4313 |
Paired t−test comparing the means at baseline and 12 months are two−sided, 95% confidence intervals (CI). All formal tests of significance are two sided with a significance level of 5%.
Abbreviations: HDL, high−density lipoprotein; LITTP, lipid intent to treat population; LDL, low-density lipoprotein; PAPL, primary analysis population for lipids; SP, secondary population. Note: variation in sample size reflects sample analysis excluded due to major protocol deviations, sample collection and study drop out over the course of 12 months.