Allergy Asthma Immunol Res.  2019 Jul;11(4):519-528. 10.4168/aair.2019.11.4.519.

Add-on Tiotropium in Chinese Patients With Moderate Asthma: A Pooled Subgroup Analysis of MezzoTinA-Asthma 1 and 2

Affiliations
  • 1Department of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, Beijing, China. jiangtao_l@263.net
  • 2Department of Pulmonary and Critical Care Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • 3Department of Pulmonary Diseases, the First Hospital of China Medical University, Shenyang, China.
  • 4Department of Pulmonary Diseases, Xinqiao Hospital, Chongqing, China.
  • 5Department of Pulmonary Diseases, the Second Xiangya Hospital of Central South University, Changsha, China.
  • 6Department of Pulmonary Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.
  • 7Department of Pulmonary Diseases, Capital Medical University Affiliated Beijing Friendship Hospital, Beijing, China.
  • 8Department of Pulmonary and Critical Care Medicine, Capital Medical University Affiliated Anzhen Hospital, Capital Medical University, Beijing, China.
  • 9Department of Pulmonary Diseases, First Affiliated Hospital of Kunming Medical University, Kunming, China.
  • 10Department of Pulmonary Diseases, Nanjing Chest Hospital, Nanjing, China.
  • 11Boehringer Ingelheim, Shanghai, China.

Abstract

PURPOSE
Asthma affects approximately 30 million patients in China; however, tiotropium data for Chinese patients is limited. This study aimed to assess the efficacy and safety of tiotropium in Chinese patients with moderate symptomatic asthma.
METHODS
A post hoc subgroup analysis was conducted on 430 Chinese patients pooled from two 24-week, replicate phase 3 trials (NCT01172808 and NCT01172821), in which they received once-daily tiotropium 2.5 µg (Tio R2.5) or 5 µg (Tio R5) (n = 106 or 109, respectively), twice-daily salmeterol 50 µg (Sal 50) (n = 110), or placebo (n = 105), while maintaining inhaled corticosteroids (ICS). The co-primary endpoints assessed in week 24 were forced expiratory volume in 1 second (FEV1) peak0-3h response, trough FEV1 response, and responder rate as assessed using the Asthma Control Questionnaire (ACQ).
RESULTS
For both FEV1 peak0-3h responses and trough FEV1 responses, the mean treatment differences were greater for Tio R2.5, Tio R5, and Sal 50 compared with placebo at 0.249 L, 0.234 L, and 0.284 L, and 0.172 L, 0.180 L, and 0.164 L, respectively (P< 0.001). The ACQ responder rate in placebo, Tio R2.5, Tio R5, and Sal 50 was 58.7%, 62.3%, 59.3%, and 69.1%, respectively. Furthermore, 11 (2.6%) of 430 patients had serious adverse events (Tio R5, n = 4; Tio R2.5, n = 1; Sal 50, n = 1; and placebo, n = 5).
CONCLUSIONS
Once-daily tiotropium, as add-on to medium-dose ICS, was effective and well tolerated for Chinese patients with moderate symptomatic asthma, consistent with the main analysis.

Keyword

Adult; asthma; Chinese; tiotropium; efficacy

MeSH Terms

Adrenal Cortex Hormones
Adult
Asian Continental Ancestry Group*
Asthma*
China
Forced Expiratory Volume
Humans
Salmeterol Xinafoate
Tiotropium Bromide*
Adrenal Cortex Hormones
Salmeterol Xinafoate
Tiotropium Bromide

Figure

  • Fig. 1 Outline of study design. ICS, inhaled corticosteroids; Tio R5, tiotropium 5 µg once-daily; Tio R2.5, tiotropium 2.5 µg once-daily; V, visit.

  • Fig. 2 Chinese patient disposition.


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