Elsevier

Respiratory Medicine

Volume 158, October–November 2019, Pages 97-109
Respiratory Medicine

Tiotropium Respimat® add-on therapy to inhaled corticosteroids in patients with symptomatic asthma improves clinical outcomes regardless of baseline characteristics

https://doi.org/10.1016/j.rmed.2019.09.014Get rights and content
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Highlights

  • Patient characteristics may impact responses to asthma treatment.

  • Tiotropium Respimat is an efficacious add-on to maintenance therapy for asthma.

  • Tiotropium improved FEV1 and asthma control irrespective of patient characteristics.

  • Once-daily add-on tiotropium Respimat is beneficial across different patient types.

Abstract

Background

Despite currently available therapies and detailed treatment guidelines, many patients with asthma remain symptomatic. Tiotropium delivered by the soft mist inhaler Respimat®, as add-on therapy to medium-dose inhaled corticosteroids (ICS), has been shown to improve lung function and asthma control in patients with symptomatic moderate asthma.

Objective

To determine whether the efficacy of tiotropium Respimat® in asthma differs by patients’ study baseline characteristics.

Methods

Two replicate Phase III, randomized, double-blind, placebo-controlled, parallel-group studies (MezzoTinA-asthma®; NCT01172808 and NCT01172821) of once-daily tiotropium Respimat 5 μg and 2.5 μg add-on to ICS were conducted in patients with symptomatic asthma despite treatment with medium-dose ICS with or without additional controllers. Subgroup analyses of peak forced expiratory volume in 1 s (FEV1), trough FEV1, risk of severe asthma exacerbation and Asthma Control Questionnaire responder rate were performed to determine whether results were influenced by patients’ baseline characteristics.

Results

In this analysis, 523 patients received placebo while 517 and 519 patients received the 5 μg and 2.5 μg dose of tiotropium Respimat, respectively. The magnitude of the improvements in lung function and asthma control, as well as the reduced risk of severe exacerbation with both doses of tiotropium Respimat versus placebo, was independent of a broad range of baseline characteristics.

Conclusions

Once-daily tiotropium Respimat as add-on to ICS is a beneficial treatment option for patients with asthma who remain symptomatic despite at least medium-dose ICS, regardless of baseline characteristics.

Keywords

Tiotropium
FEV1
Respimat
Exacerbation
Asthma Control Questionnaire

Abbreviations

ACQ-7
7-question Asthma Control Questionnaire
AE
adverse event
BMI
body mass index
CI
confidence interval
FEV1
forced expiratory volume in 1 s
FEV1(0–3h)
FEV1 from baseline 0–3 h post-dose
FVC
forced vital capacity
GINA
Global Initiative for Asthma
HR
hazard ratio
ICS
inhaled corticosteroid
IgE
immunoglobulin E
OR
odds ratio
LABA
long-acting β2-agonist
LTRA
leukotriene receptor antagonist
MMRM
mixed model repeated measures
PEF
peak expiratory flow
T2
type 2
TALC
Tiotropium Bromide as an Alternative to Increased Inhaled Glucocorticoid in Patients Inadequately Controlled on a Lower Dose of Inhaled Corticosteroid

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