Selective Estrogen Receptor Modulators Breast Cancer Prevention TrialInterest of breast cancer chemoprevention was generated by the finding that the selective estrogen receptor modulator (SERM), tamoxifen, when used as adjuvant therapy of both pre-and postmenopausal women with Introduction Breast cancer is the most common cancer in women. The term "chemoprevention" describes interventions used in women with no prior breast cancer to reduce breast cancer risk. 1 However, given that breast cancers take years to develop and become clinically detectable, can chemoprevention administered for a relatively short time of 3 or 5 years interfere with such a long--term process? Santen et al.2 addressed this issue using a clinically based model, an average 200 -day time of breast cancer doubling, 1.16 cm breast cancer detection threshold for mammography, and a 7% prevalence of subclinical breast cancer in postmenopausal women based on autopsy series. This model was applied to a population from the Women's Health Initiative (WHI) randomized trial evaluating estrogen plus progestin, 3 which involved a population quite similar to that participating in most breast cancer
ABSTRACTIn Western countries, breast cancer is the most common cancer in women but available interventions can reduce risk. The aim of the paper was to review the available evidence regarding breast cancer chemoprevention trials. A systematic literature search was conducted to identify all full -scale, randomized prospective chemoprevention trials as well as similarly conducted randomized trials with breast cancer as the primary monitoring endpoint. In full -scale, randomized chemoprevention trials, the selective estrogen receptor modulators (SERMs), tamoxifen and raloxifene, reduce breast cancer incidence. In a direct comparison, tamoxifen resulted in greater breast cancer reduction than raloxifene but with greater endometrial cancer risk. The aromatase inhibitors, exemestane and anastrozole, also reduce breast cancer incidence in breast cancer prevention trials. In the Women's Health Initiative hormone therapy trials, in postmenopausal women with no prior hysterectomy, estrogen plus progestin increased breast cancer incidence and deaths from breast cancer, while estrogen alone, in women with prior hysterectomy, reduced breast cancer incidence and reduced deaths from breast cancer. For premenopausal women at increased breast cancer risk, tamoxifen is a proven option with favorable side effect profile. For postmenopausal women, while no direct comparison of SERMs and aromatase inhibitors for chemoprevention are available, cross -study comparisons suggest greater efficacy and more favorable side effect profile for aromatase inhibitor use, especially for older women. The opposite effects of estrogen plus progestin compared with estrogen alone on breast cancer incidence and outcome should factor into risk -benefit consideration when these agents are considered for climacteric symptom management. 39-3.42; P = 0.001), thromboembolic disease (HR, 1.60; 95% CI, 1.2...