Menopause The Journal of The North American Menopause Society · 2024 · 14 citations · 27 references
PharmacyPharmacologyPharmacotherapyOutcomes ResearchReproductive EndocrinologyWomen's HealthClinical TrialsMenopause CareMenopause Hormone TherapyMenopause ManagementMenopause PharmacotherapyTreatment Response MonitoringClinically Meaningful ChangeMenopausal Symptom ReliefMenopause Symptom ManagementPatient-reported Outcome MeasurementPlacebo-controlled Efficacy AssessmentVasomotor DysfunctionVasomotor Symptom ManagementVasomotor Symptoms
OBJECTIVES: The aims of the study were to further characterize the efficacy of fezolinetant for the treatment of moderate-to-severe vasomotor symptoms (VMS) due to menopause using responder analysis and to investigate whether efficacy, not adjusted for placebo, resulted in clinically meaningful within-patient change. METHODS: This prespecified analysis used pooled data from two phase 3, randomized, double-blind, placebo-controlled studies (SKYLIGHT 1 and 2). Responders were those experiencing ≥50%, ≥75%, ≥90%, or 100% reduction in VMS frequency from baseline to weeks 4 and 12. Responder analysis was performed for patient-reported outcome (PRO) measures to evaluate participants achieving a clinically meaningful within-patient change (not placebo adjusted) at week 4 and 12 versus baseline. Single responders were based on outcomes of VMS frequency, Patient-Reported Outcomes Measurement Information System Sleep Disturbance-Short Form 8b Total Score, Menopause-Specific Quality of Life (MENQoL) Total Score, and MENQoL VMS Domain Score. Double and triple responder analyses combined VMS frequency plus one or more of the PRO. Patient Global Impression of Change VMS was deemed a suitable anchor measure for meaningful within-patient change in VMS frequency. RESULTS: A greater proportion of fezolinetant-treated versus placebo-treated participants had ≥50%, ≥75%, ≥90%, or 100% reduction in VMS frequency from baseline to weeks 4 and 12. A greater proportion of responders were observed in the fezolinetant groups versus placebo at week 12 in all four single responder analyses. In the double and triple responder analyses, odds ratios were supportive of a beneficial effect for both doses of fezolinetant versus placebo. CONCLUSIONS: Fezolinetant was associated with significantly higher within-patient clinically meaningful improvement in important PRO, including VMS frequency, PROMIS SD SF 8b Total Score, MENQoL Total Score, and MENQoL VMS Domain Score.
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Duration of Menopausal Vasomotor Symptoms Over the Menopause Transition
Nancy E. Avis, Sybil L. Crawford, Gail A. Greendale et al. · JAMA Internal Medicine · 2015 · 974 citations · Full text
Medicine, Endocrinology, Gynecology +17
Ellen B. Gold, Alicia Colvin, Nancy E. Avis et al. · American Journal of Public Health · 2006 · 918 citations · Full text
Medicine, Endocrinology, Gynecology +17
A menopause-specific quality of life questionnaire: development and psychometric properties
John R. Hilditch, Jacqueline Lewis, Alice Peter et al. · Maturitas · 1996 · 747 citations
Medicine, Endocrinology, Gynecology +16
A menopause-specific quality of life questionnaire: development and psychometric properties
John R. Hilditch, Jacqueline Lewis, Alice Peter et al. · Maturitas · 1996 · 480 citations
Medicine, Endocrinology, Gynecology +16