TABLE 2.
Absolute difference | Adverse events | ||||||
---|---|---|---|---|---|---|---|
Drug | DFS | OS | Hot flashes | Endometrial cancer | Thromboembolic events | Bone fracture/ osteoporosis | Trial |
Anastrozole vs. tamoxifen | 2.4% | 0.3% | 36% | 0.2%* | 4.5%* | 11%† | ATAC, AIs started immediately postsurgery; 3,215 patients in the anastrozole arm, 3,116 in the tamoxifen arm |
Letrozole vs. tamoxifen | 1.9% | 0.7% | 34% | 0.2% | 2.0%* | 5.8%* | BIG 01-198, AIs started immediately postsurgery; 4,003 patients in the letrozole arm, 4,007 in the tamoxifen arm |
Exemestane vs. tamoxifen | 3.5% | 0.6% | 42% | NR | 1.9%* | 7.4%* | IES, AIs started after 2 to 3 yrs of tamoxifen; 2,362 patients in the exemestane arm, 2,372 in the tamoxifen arm |
AI=aromatase inhibitors; ATAC=arimidex, tamoxifen alone or in combination; BIG=Breast International Group; DFS=disease-free survival; IES=International Exemestane Study; NR=not reported; OS=overall survival.
Difference statistically significant in favor of AI.
Difference statistically significant in favor of tamoxifen.
Table should not be used to compare AIs, as trial designs differed. These agents’ comparisons to tamoxifen are valid only in the context of each individual trial.
Sources: Nordman 2005, Masakazu 2006