Peters F
Department of Obstetrics and Gynecology, St Hildegardis Hospital, Johannes Gutenberg University, Mainz, Germany.
Lancet. 1992 Jan 25;339(8787):205-8. doi: 10.1016/0140-6736(92)90005-n.
Although the aetiology of cyclical mastalgia is poorly understood, the consistent finding of an increased prolactin stimulation response probably due to oestrogen dominance has led to the use of treatment with prolactin-lowering drugs and antioestrogens. The efficacy and safety in cyclical mastalgia of gestrinone, which has androgenic, anti-oestrogenic, and antiprogestagenic properties, were investigated in a multicentre study. In a double-blind randomisation procedure, 72 patients were allocated placebo and 73 treatment with gestrinone (2.5 mg twice a week) for 3 months. The patients recorded the severity of breast pain on a visual analogue scale before and during treatment and scored other breast symptoms as not present (0), mild (1), moderate (2), or severe (3). The gestrinone group had significantly greater reductions than the placebo group in breast pain score at months 1, 2, and 3 of treatment (mean reduction 59.5 [SD 22.6] to 11.7 [17.0] vs 58.2 [17.6] to 36.7 [23.0] at month 3; p less than 0.0001). All six breast symptoms had lower scores in the gestrinone than in the placebo group by the end of treatment. In a subset of 30 participants (15 from each group), serum concentrations of oestradiol, progesterone, and tri-iodothyronine were significantly lower than baseline after 3 months of gestrinone, but concentrations of luteinising hormone, follicle-stimulating hormone, prolactin, thyroid-stimulating hormone, and thyroxine did not change. 41% of gestrinone-treated and 14% of placebo-treated patients reported at least one side-effect; most of these were androgen-mediated. 11 placebo-treated patients and 4 on gestrinone discontinued treatment. Thus, gestrinone was very effective in the treatment of cyclical mastalgia and was well tolerated.
尽管周期性乳痛的病因尚不清楚,但一直发现催乳素刺激反应增加,这可能是由于雌激素占主导地位所致,因此人们开始使用降低催乳素的药物和抗雌激素药物进行治疗。孕三烯酮具有雄激素、抗雌激素和抗孕激素特性,一项多中心研究对其治疗周期性乳痛的疗效和安全性进行了调查。在双盲随机程序中,72例患者被分配接受安慰剂治疗,73例患者接受孕三烯酮(每周两次,每次2.5mg)治疗,为期3个月。患者在治疗前和治疗期间用视觉模拟量表记录乳房疼痛的严重程度,并将其他乳房症状评为不存在(0)、轻度(1)、中度(2)或重度(3)。孕三烯酮组在治疗第1、2和3个月时乳房疼痛评分的降低幅度明显大于安慰剂组(第3个月时平均降低幅度为59.5[标准差22.6]至11.7[17.0],而安慰剂组为58.2[17.6]至36.7[23.0];p<0.0001)。到治疗结束时,孕三烯酮组所有六项乳房症状的评分均低于安慰剂组。在30名参与者(每组15名)的子集中,孕三烯酮治疗3个月后,雌二醇、孕酮和三碘甲状腺原氨酸的血清浓度显著低于基线水平,但促黄体生成素、促卵泡激素、催乳素、促甲状腺激素和甲状腺素的浓度没有变化。接受孕三烯酮治疗的患者中有41%、接受安慰剂治疗的患者中有14%报告至少出现一种副作用;其中大多数是雄激素介导的。11名接受安慰剂治疗的患者和4名接受孕三烯酮治疗的患者停止了治疗。因此,孕三烯酮治疗周期性乳痛非常有效,且耐受性良好。