Long-term safety and efficacy of antimuscarinic add-on therapy in patients with overactive bladder who had a suboptimal response to mirabegron monotherapy: A multicenter, randomized study in Japan (MILAI II study).


Journal

International journal of urology : official journal of the Japanese Urological Association
ISSN: 1442-2042
Titre abrégé: Int J Urol
Pays: Australia
ID NLM: 9440237

Informations de publication

Date de publication:
03 2019
Historique:
received: 04 07 2018
accepted: 15 10 2018
pubmed: 15 12 2018
medline: 17 6 2020
entrez: 15 12 2018
Statut: ppublish

Résumé

To evaluate the long-term safety (primary objective) and efficacy (secondary objective) of antimuscarinic add-on therapy in patients receiving mirabegron. During a 2-week screening period, patients (aged ≥20 years, mirabegron treatment for ≥6 weeks, residual overactive bladder symptoms) received mirabegron 50 mg once daily. These patients were subsequently randomized to 52 weeks' treatment with mirabegron 50 mg/day plus an antimuscarinic (solifenacin 5 mg, propiverine 20 mg, imidafenacin 0.2 mg, or tolterodine 4 mg) with the potential to double the antimuscarinic dose (except for tolterodine) at week 8. Safety assessments included treatment-emergent adverse events, vital signs, 12-lead electrocardiograms, post-void residual volume, and laboratory evaluations. Efficacy was assessed using changes from baseline in overactive bladder symptom score total score; overactive bladder questionnaire short form score; micturitions, urgency episodes, urinary incontinence episodes, and urgency urinary incontinence episodes/24 h; mean volume voided per micturition; and number of night-time micturitions. Overall, 80.2% of patients (88.1% women, mean age 65 years) experienced at least one treatment-emergent adverse event, with similar rates for all treatments. The adverse events most commonly reported were dry mouth, nasopharyngitis, and constipation. No marked change was observed in systolic or diastolic blood pressure for any treatment, although pulse rate increased slightly in the mirabegron and propiverine, and mirabegron and tolterodine groups. For all treatments, significant improvements were observed in all efficacy parameters, including overactive bladder symptom score total and questionnaire short form scores. Antimuscarinic add-on therapy is well tolerated and effective after initial treatment with mirabegron in patients with overactive bladder symptoms.

Identifiants

pubmed: 30548692
doi: 10.1111/iju.13868
pmc: PMC7379522
doi:

Substances chimiques

Acetanilides 0
Adrenergic beta-3 Receptor Agonists 0
Benzilates 0
Imidazoles 0
Muscarinic Antagonists 0
Thiazoles 0
propiverine 468GE2241L
Tolterodine Tartrate 5T619TQR3R
Solifenacin Succinate KKA5DLD701
mirabegron MVR3JL3B2V
imidafenacin XJR8Y07LJO

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

342-352

Subventions

Organisme : Astellas Pharma Inc.
Pays : International

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2018 The Authors. International Journal of Urology published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Urological Association.

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Auteurs

Osamu Yamaguchi (O)

Department of Chemical Biology and Applied Chemistry, Nihon University School of Engineering, Koriyama, Japan.

Hidehiro Kakizaki (H)

Department of Urology, Asahikawa Medical University, Asahikawa, Japan.

Yukio Homma (Y)

Department of Urology, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.

Yasuhiko Igawa (Y)

Department of Continence Medicine, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.

Masayuki Takeda (M)

Department of Urology, Graduate Faculty of Interdisciplinary Research, University of Yamanashi, Chuo, Japan.

Osamu Nishizawa (O)

Department of Urology, North Alps Medical Center, Azumi Hospital, Nagano, Japan.

Momokazu Gotoh (M)

Department of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Masaki Yoshida (M)

Department of Urology, National Center for Geriatrics and Gerontology, Obu, Japan.

Osamu Yokoyama (O)

Department of Urology, University of Fukui Faculty of Medical Sciences, Fukui, Japan.

Narihito Seki (N)

Department of Urology, Kyushu Central Hospital of the Mutual Aid Association of Public School Teachers, Fukuoka, Japan.

Akira Okitsu (A)

Astellas Pharma Inc., Tokyo, Japan.

Takuya Hamada (T)

Astellas Pharma Inc., Tokyo, Japan.

Akiko Kobayashi (A)

Astellas Pharma Inc., Tokyo, Japan.

Kentaro Kuroishi (K)

Astellas Pharma Inc., Tokyo, Japan.

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