TY - JOUR
T1 - Paroxetine is an effective treatment for hot flashes
T2 - Results from a prospective randomized clinical trial
AU - Stearns, Vered
AU - Slack, Rebecca
AU - Greep, Nancy
AU - Henry-Tilman, Ronda
AU - Osborne, Michael
AU - Bunnell, Craig
AU - Ullmer, Lynda
AU - Gallagher, Ann
AU - Cullen, Jennifer
AU - Gehan, Edmund
AU - Hayes, Daniel F.
AU - Isaacs, Claudine
PY - 2005/12/1
Y1 - 2005/12/1
N2 - Purpose: 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. Patients and Methods :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. Results: 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). Conclusion: Paroxetine is an effective treatment for hot flashes in women with or without a prior breast cancer.
AB - Purpose: 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. Patients and Methods :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. Results: 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). Conclusion: Paroxetine is an effective treatment for hot flashes in women with or without a prior breast cancer.
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U2 - 10.1200/JCO.2005.10.081
DO - 10.1200/JCO.2005.10.081
M3 - Article
C2 - 16192581
AN - SCOPUS:27244436938
SN - 0732-183X
VL - 23
SP - 6919
EP - 6930
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 28
ER -