Abstract
Tamoxifen as adjuvant therapy for women with breast cancer decreases serum lipids and lipoproteins by its estrogenic agonist effects. We evaluated whether a novel antiestrogen, toremifene, has similar effects. Patients and Methods 49 postmenopausal early breast cancer patients were randomized to adjuvant tamoxifen or toremifene treatment groups. Total, LDL and HDL cholesterol, apolipoprotein A-I, A-II and B and Lp(a) were measured before treatment and after 12 months. Results Both antiestrogens reduced significantly serum total and LDL cholesterol and apo B levels. The response of HDL cholesterol to treatment was clearly different between the groups. Toremifene increased the HDL-Ievel 14% whereas tamoxifen decreased it 5% ( P = 0.001). Both Chol/HDL and LDL/HDL ratios fell more in the toremifene than tamoxifen group (P = 0.008; p = 0.03, respectively). Toremifene also increased apo A-I level ( P = 0.00007) and apo A-I/A-II ratio ( P = 0.018). In both tamoxifen and toremifene treatment groups Lp(a) concentration fell significantly (change: 34% vs 41%). Conclusion These results provide positive evidence that toremifene has highly antiatherogenic properties with an exceptional potency to improve all lipoproteins which are associated with increased coronary heart disease risk.
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