Ettinger D S, Allegra J, Bertino J R, Bonomi P, Browder H, Byrne P, Carpenter J, Catalano R, Creech R, Dana B
Semin Oncol. 1986 Dec;13(4 Suppl 4):9-14.
This report describes the preliminary results from a randomized study comparing megestrol acetate with tamoxifen in the treatment of postmenopausal women with advanced breast cancer, correlating estrogen receptors (ER) and progesterone receptor (PgR) status with response. Patients received megestrol acetate (40 mg) orally four times daily or tamoxifen (10 mg) orally twice daily. If the initial therapy failed, patients were crossed over to the alternate treatment. Of 197 patients entered in the study, 190 were considered evaluable. The overall response rates were 35% with megestrol acetate and 42% with tamoxifen. Twenty-three percent (7/30) of patients responded to megestrol acetate after being crossed over from tamoxifen, while 22% (6/27) responded to tamoxifen after being crossed over from megestrol acetate. Response did not correlate significantly with combined receptor (ie, ER plus PgR) levels. A significant trend was seen between ER level and response only in the tamoxifen group. There was no association between PgR levels and response for either tamoxifen or megestrol acetate.
本报告描述了一项随机研究的初步结果,该研究比较了醋酸甲地孕酮与他莫昔芬在治疗绝经后晚期乳腺癌女性中的疗效,并将雌激素受体(ER)和孕激素受体(PgR)状态与反应相关联。患者接受每日口服4次醋酸甲地孕酮(40毫克)或每日口服2次他莫昔芬(10毫克)。如果初始治疗失败,患者交叉接受替代治疗。在197名进入该研究的患者中,190名被认为可评估。醋酸甲地孕酮的总体缓解率为35%,他莫昔芬为42%。从他莫昔芬交叉接受醋酸甲地孕酮治疗的患者中有23%(7/30)对醋酸甲地孕酮有反应,而从醋酸甲地孕酮交叉接受他莫昔芬治疗的患者中有22%(6/27)对他莫昔芬有反应。反应与联合受体(即ER加PgR)水平无显著相关性。仅在他莫昔芬组中,ER水平与反应之间存在显著趋势。对于他莫昔芬或醋酸甲地孕酮,PgR水平与反应均无关联。