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

被引:3
|
作者
Grenabo, Lars [1 ]
Herschorn, Sender [2 ]
Kaplan, Steven A. [3 ]
Cardozo, Linda [4 ]
Scholfield, David [5 ]
Arumi, Daniel [6 ]
Carlsson, Martin [7 ]
Chapman, Douglass [7 ]
Ntanios, Fady [7 ]
机构
[1] Univ Gothenburg, Dept Urol, Gothenburg, Sweden
[2] Univ Toronto, Dept Urol, Toronto, ON, Canada
[3] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[4] Kings Coll Hosp London, Dept Urogynaecol, London, England
[5] Pfizer Ltd, Sandwich, Kent, England
[6] Pfizer Europe, Madrid, Spain
[7] Pfizer Inc, New York, NY USA
关键词
Overactive bladder; urgency urinary incontinence; treatment response; antimuscarinics; fesoterodine; tolterodine; TOLTERODINE EXTENDED-RELEASE; QUALITY-OF-LIFE; HEAD-TO-HEAD; 8; MG; FESOTERODINE; EFFICACY; PREDICT; AGENTS; ONSET;
D O I
10.1080/03007995.2017.1361914
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To assess the characteristics of tolterodine extended-release (ER) 4mg 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 8mg 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 4mg during a 2 week run-in. Suboptimal responders after tolterodine treatment (week 0) were randomized to fesoterodine (4mg for 1 week, 8mg 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 8mg 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 8mg. No antimuscarinic use before tolterodine and fewer baseline UUI episodes were significant predictors of a UUI response with fesoterodine.
引用
收藏
页码:1731 / 1736
页数:6
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