Stearns Vered, Slack Rebecca, Greep Nancy, Henry-Tilman Ronda, Osborne Michael, Bunnell Craig, Ullmer Lynda, Gallagher Ann, Cullen Jennifer, Gehan Edmund, Hayes Daniel F, Isaacs Claudine
Lombardi Comprehensive Cancer Center at Georgetown University, Washington, DC, USA.
J Clin Oncol. 2005 Oct 1;23(28):6919-30. doi: 10.1200/JCO.2005.10.081.
In an open-label trial we have previously demonstrated that paroxetine reduces hot flashes. We initiated a stratified, randomized, double-blind, cross-over, placebo-controlled trial to investigate the efficacy of paroxetine 10 mg and 20 mg compared to placebo in reducing hot flash frequency and composite score. A secondary objective was to evaluate quality of life (QOL) parameters.
Women who suffered at least two hot flashes a day for 1 month or longer were eligible. Women were randomly assigned to 4 weeks of paroxetine 10 mg or 20 mg followed by placebo for 4 weeks, or placebo for 4 weeks followed by paroxetine 10 mg or 20 mg for 4 weeks. Participants completed baseline daily hot flash diaries for one week prior to the start of the study and throughout the study, and QOL questionnaires at baseline, week 5 and week 9.
279 women were screened, and 151 were randomly assigned. Paroxetine 10 mg reduced hot flash frequency and composite score by 40.6% and 45.6%, respectively, compared to 13.7% and 13.7% for placebo (P = .0006 and P = .0008, respectively). Paroxetine 20 mg reduced hot flash frequency and composite score by 51.7% and 56.1%, respectively, compared with 26.6% and 28.8% for placebo (P = .002 and P = .004, respectively). Efficacy was similar between the two doses, but women were less likely to discontinue low-dose paroxetine. Paroxetine 10 mg was associated with a significant improvement in sleep compared with placebo (P = .01).
Paroxetine is an effective treatment for hot flashes in women with or without a prior breast cancer.
在一项开放标签试验中,我们之前已证明帕罗西汀可减少潮热。我们启动了一项分层、随机、双盲、交叉、安慰剂对照试验,以研究10毫克和20毫克帕罗西汀与安慰剂相比在降低潮热频率和综合评分方面的疗效。次要目标是评估生活质量(QOL)参数。
每天至少经历两次潮热持续1个月或更长时间的女性符合条件。女性被随机分配接受4周的10毫克或20毫克帕罗西汀治疗,随后4周接受安慰剂治疗,或4周接受安慰剂治疗,随后4周接受10毫克或20毫克帕罗西汀治疗。参与者在研究开始前一周及整个研究过程中完成每日潮热日记,并在基线、第5周和第9周完成QOL问卷。
筛查了279名女性,151名被随机分配。与安慰剂组分别降低13.7%和13.7%相比,10毫克帕罗西汀使潮热频率和综合评分分别降低了40.6%和45.6%(P分别为0.0006和0.0008)。与安慰剂组分别降低26.6%和28.8%相比,20毫克帕罗西汀使潮热频率和综合评分分别降低了51.7%和56.1%(P分别为0.002和0.004)。两剂量组疗效相似,但女性停用低剂量帕罗西汀的可能性较小。与安慰剂相比,10毫克帕罗西汀与睡眠显著改善相关(P = 0.01)。
帕罗西汀是有或无乳腺癌病史女性潮热的有效治疗方法。