From:  De novo cholesterol biosynthesis: an additional therapeutic target for the treatment of postmenopausal breast cancer with excessive adipose tissue

Randomized trials of tamoxifen vs. AIs in the adjuvant breast cancer setting

Clinical trial comparison(s)N. of cases(menopausal status)Follow (years)upOverall resultsPredictive effects by BMIReferences
ATAC
A vs. T
4,939 (post)8.3A better than TA better than T at all BMI levels
A less effective when BMI ≥ 30 for DDFS
A relative benefit of A vs. T when BMI low
[7]
TEAM
E vs. T → E
4,700 (post)5.1E = T
95% CI (0.39–0.84)
E better than T (2.75 years) at all BMI levels, significant in BMI > 30 (DDFS HR = 0.57, 95% CI = 0.39–0.84)
E better than T → E (5.1 years) for any BMI (ns), BMI > 30 (DDFS HR = 0.75, 95% CI = 0.56–1.01 and OS HR = 0.71, 95% CI = 0.51–1.01)
[10]
ABCSG-12
A + G vs. T + G
1,684 (pre)5.2A + G = T + G (DFS)
A + G worse than T + G (OS)
BMI < 25: A = T (DFS, OS)
BMI ≥ 25: A worse than T
HR = 1.49, 95% CI = 0.93–2.03 (DFS)
HR = 3.03, 95% CI = 1.35–6.82 (OS)
[8]
BIG 1–98
L vs. T vs.
L → T vs. T → L
4,760 (post)8.7L better than T
(DFS, DDFS, OS)
L → T or T → L = L
Treatment by BMI interactions (ns)
L vs. T HR: 0.77 NW, 0.68 OW, 0.78 OB
[11]

N.: number of cases; A: anastrozole; T: tamoxifen; L: letrozole; E: exemestane; G: goserelin; T → E: tamoxifen followed by exemestane; L → T: letrozole followed by tamoxifen; T → L: tamoxifen followed by letrozole; BIG 1–98: breast international group 1–98 trial; NW: normal weight; OW: overweight; OB: obese; DDFS: distant disease-free survival; DFS: disease-free survival; OS: overall survival; ns: not significant