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托瑞米芬治疗经前乳痛的女性的乳腺磁共振成像结果

Breast magnetic resonance imaging findings in women treated with toremifene for premenstrual mastalgia.

作者信息

Oksa S, Parkkola R, Luukkaala T, Mäenpää J

机构信息

Department of Obstetrics and Gynecology, Satakunta Central Hospital, Pori, Finland.

出版信息

Acta Radiol. 2009 Nov;50(9):984-9. doi: 10.3109/02841850903168083.

Abstract

BACKGROUND

Toremifene, a selective estrogen receptor modulator, has been shown to be effective in alleviating premenstrual breast pain. However, the exact mechanism by which toremifene and related compounds work in premenstrual mastalgia is poorly understood.

PURPOSE

To find out if the effect of toremifene on breast would be detectable with dynamic magnetic resonance imaging (MRI).

MATERIAL AND METHODS

This randomized, double-blind crossover study was performed on women suffering from marked premenstrual mastalgia. Ten women were randomized to receive either toremifene (20 mg) or placebo from cycle day 15 until next menstruation for three menstrual cycles. After a washout period, the treatment was crossed over for three additional cycles. The MRI evaluations were performed premenstrually at the end of each treatment phase. Breast pain and quality-of-life scores were collected from one baseline cycle and from all the treatment cycles.

RESULTS

Nine patients were evaluable for this analysis. Both the enhancement ratio and the maximum slope of enhancement tended to be smaller during the toremifene cycles as compared to placebo. On the left side, the difference in the maximum slope of enhancement between toremifene and placebo was statistically significant (median 5.150 [range 3.7-6.7] and 6.500 [range 4.9-9.5], respectively; P=0.047). T2 relaxation times as well as breast pain and quality-of-life scores were inconsistent.

CONCLUSION

Use of toremifene is associated with measurable changes in dynamic breast MRI findings in women with cyclic breast pain.

摘要

背景

托瑞米芬是一种选择性雌激素受体调节剂,已被证明可有效缓解经前乳房疼痛。然而,托瑞米芬及相关化合物在经前乳房疼痛中的确切作用机制尚不清楚。

目的

通过动态磁共振成像(MRI)来确定托瑞米芬对乳房的影响是否可检测到。

材料与方法

本随机、双盲交叉研究针对患有明显经前乳房疼痛的女性进行。10名女性被随机分配,从月经周期第15天开始至下次月经,接受托瑞米芬(20mg)或安慰剂治疗,为期三个月经周期。经过洗脱期后,治疗方案交叉再进行三个周期。在每个治疗阶段结束时于经前进行MRI评估。收集一个基线周期以及所有治疗周期的乳房疼痛和生活质量评分。

结果

9名患者可纳入本分析。与安慰剂相比,托瑞米芬治疗周期内的增强率和最大增强斜率均趋于较小。在左侧,托瑞米芬与安慰剂之间的最大增强斜率差异具有统计学意义(中位数分别为5.150[范围3.7 - 6.7]和6.500[范围4.9 - 9.5];P = 0.047)。T2弛豫时间以及乳房疼痛和生活质量评分并不一致。

结论

对于患有周期性乳房疼痛的女性,使用托瑞米芬与动态乳腺MRI结果的可测量变化相关。

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