Grenabo Lars, Herschorn Sender, Kaplan Steven A, Cardozo Linda, Scholfield David, Arumi Daniel, Carlsson Martin, Chapman Douglass, Ntanios Fady
a Department of Urology , University of Gothenburg , Gothenburg , Sweden.
b Department of Urology , University of Toronto , Toronto , Canada.
Curr Med Res Opin. 2017 Oct;33(10):1731-1736. doi: 10.1080/03007995.2017.1361914. Epub 2017 Aug 29.
To assess the characteristics of tolterodine extended-release (ER) 4 mg responders and suboptimal responders (≤50% decrease in UUI episodes/24 h) among patients with overactive bladder (OAB), including urgency urinary incontinence (UUI), and identify predictors of a >50% UUI response with fesoterodine 8 mg in tolterodine suboptimal responders.
Adult patients with OAB symptoms for ≥6 months and ≥8 micturitions, and ≥2 and <15 UUI episodes/24 h at week -2 received open-label tolterodine ER 4 mg during a 2 week run-in. Suboptimal responders after tolterodine treatment (week 0) were randomized to fesoterodine (4 mg for 1 week, 8 mg for weeks 2-12) or placebo once daily. Post-hoc analyses compared the percentage change from week -2 to week 0 in UUI episodes/24 h in tolterodine responders versus suboptimal responders and identified significant predictors of a UUI response at week 12 with fesoterodine 8 mg among tolterodine suboptimal responders.
Of 897 patients, 610 (68%) were UUI suboptimal responders during the run-in period. UUI episodes/24 h at week -2 were similar in tolterodine responders and suboptimal responders (4.2 vs. 4.3), but responders showed a significantly greater median percentage decrease in UUI episodes/24 h after tolterodine treatment at week 0 (80.0% versus 15.3%; p < .0001). During double-blind treatment, the percentage of patients with a UUI response at week 12 was significantly greater with fesoterodine (69.9%) than placebo (57.0%; p = .0027). Fesoterodine (vs. placebo), no previous antimuscarinic use before tolterodine run-in, and less UUI severity at baseline were significant predictors of a UUI response.
For patients with OAB, including UUI, who were treated initially with tolterodine and showed a suboptimal UUI response, nearly 70% demonstrated a UUI response with second-line fesoterodine 8 mg. No antimuscarinic use before tolterodine and fewer baseline UUI episodes were significant predictors of a UUI response with fesoterodine.
评估膀胱过度活动症(OAB)患者(包括急迫性尿失禁(UUI))中托特罗定缓释(ER)4mg反应者和反应欠佳者(UUI发作次数/24小时减少≤50%)的特征,并确定托特罗定反应欠佳者中使用非索罗定8mg后UUI反应>50%的预测因素。
有OAB症状≥6个月、排尿次数≥8次、在第-2周时UUI发作次数≥2次且<15次/24小时的成年患者,在为期2周的导入期接受开放标签的托特罗定ER 4mg治疗。托特罗定治疗后(第0周)反应欠佳者被随机分为非索罗定组(第1周4mg,第2 - 12周8mg)或安慰剂组,每日一次。事后分析比较了托特罗定反应者与反应欠佳者从第-2周到第0周UUI发作次数/24小时的百分比变化,并确定了托特罗定反应欠佳者中在第12周使用非索罗定8mg后UUI反应的显著预测因素。
897例患者中,610例(68%)在导入期为UUI反应欠佳者。第-2周时托特罗定反应者和反应欠佳者的UUI发作次数/24小时相似(4.2次对4.3次),但反应者在第0周托特罗定治疗后UUI发作次数/24小时的中位数百分比下降显著更大(80.0%对15.3%;p <.0001)。在双盲治疗期间,第12周时非索罗定组UUI反应患者的百分比显著高于安慰剂组(69.9%对57.0%;p = 0.0027)。非索罗定(与安慰剂相比)、在托特罗定导入期之前未使用过抗毒蕈碱药物以及基线时UUI严重程度较低是UUI反应的显著预测因素。
对于最初接受托特罗定治疗且UUI反应欠佳的OAB患者(包括UUI患者),近70%的患者使用二线药物非索罗定8mg后有UUI反应。在托特罗定之前未使用过抗毒蕈碱药物以及基线时UUI发作次数较少是使用非索罗定后UUI反应的显著预测因素。