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膀胱过度活动症患者随机临床试验中抗毒蕈碱反应者与反应欠佳者的特征

Characteristics of antimuscarinic responders versus suboptimal responders in a randomized clinical trial of patients with overactive bladder symptoms.

作者信息

Grenabo Lars, Herschorn Sender, Kaplan Steven A, Cardozo Linda, Scholfield David, Arumi Daniel, Carlsson Martin, Chapman Douglass, Ntanios Fady

机构信息

a Department of Urology , University of Gothenburg , Gothenburg , Sweden.

b Department of Urology , University of Toronto , Toronto , Canada.

出版信息

Curr Med Res Opin. 2017 Oct;33(10):1731-1736. doi: 10.1080/03007995.2017.1361914. Epub 2017 Aug 29.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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