Efficacy and safety of tiotropium bromide combined with budesonide/formoterol in the treatment of moderate to severe chronic obstructive pulmonary disease.

With the increase of environmental pollution, chronic obstructive pulmonary disease (COPD) has become a serious health threat. In the present study, the efficacy and safety of inhalation therapy of tiotropium bromide combined with budesonide/formoterol were assessed in 180 patients with moderate to severe COPD (clinical trial registry no. ChiCTR1800017584). Patients were treated by inhalation of budesonide/formoterol (control group) or inhalation of tiotropium bromide combined with budesonide/formoterol (intervention group). The results indicated that after the treatment, the forced expiratory volume in 1 sec, the modified Medical Research Council scale, the 6-min walking distance and the St. George's Respiratory Questionnaire scores for quality of life were significantly improved in the two groups, while the improvements in the intervention group were more significant (all P<0.05). There was no significant difference in body mass indices between the two groups during the course of the treatment (P=0.302). The difference in the risk of an acute exacerbation between the two groups was also not significant (P=0.238). The median time to the first acute exacerbation from the start of treatment in the intervention group (53 days; 25% quartile, 50 days; 75% quartile, 62 days) was significantly longer than that in the control group (37 days; 25% quartile, 23 days; 75% quartile, 39 days; P=0.042). The adverse reaction rates in the intervention and control groups were 14.4 and 10.0%, respectively, without any significant difference. In conclusion, inhalation treatment of tiotropium bromide combined with budesonide/formoterol significantly improves pulmonary function, exercise capacity and quality of life of patients with COPD compared with budesonide/formoterol inhalation alone, while the effect of reducing the acute attack risk requires further evaluation.

RCT Entities:   Population Interventions Outcomes

Introduction

With the continuous progression of aging, severe air pollution and high smoking rate, chronic obstructive pulmonary disease (COPD) has become a serious health threat in China. In 2013, the prevalence rate of COPD in people >40 years was 7.3%, making it a leading cause of disability, and it seriously affects the quality of life of affected patients (1,2). As a chronic lung disease, COPD comprises an incompletely reversible airflow limitation and develops progressively. Therefore, the major purpose of treatment is to relieve symptoms, reduce exacerbation, and improve lung function and quality of life. The commonly used medications for COPD include inhaled glucocorticoids, methylxanthines and bronchodilators (including cholinolytic agents and β2 receptor agonists); at present, multiple COPD treatment guidelines recommend combined application of different types of bronchodilators or application of bronchodilators combined with inhaled glucocorticoids (3,4).

Tiotropium bromide is a long-acting cholinolytic bronchodilator. Studies have indicated that tiotropium alone improves lung function and quality of life, and reduces the risk of acute attack; in addition, long-term inhalation of tiotropium bromide and salmeterol/fluticasone reduces the frequency of acute exacerbation of COPD and the risk of mortality, and improves the health-associated quality of life of affected patients (5,6). However, the combined application of tiotropium bromide and β2 receptor agonist bronchodilators or glucocorticoids remains controversial (7). Previous studies assessing inhalation therapy of tiotropium bromide combined with budesonide/formoterol have provided conflicting results (8,9). Therefore, the present study aimed to further evaluate the efficacy and safety of tiotropium bromide combined with budesonide/formoterol in patients with moderate to severe COPD.

Patients and methods

Subjects

The present study was approved by the Ethics Committee of the First Affiliated Hospital of Soochow University (Suzhou, China). A total of 180 patients with moderate to severe COPD (groups B and C) in the stable phase treated at the First Affiliated Hospital of Soochow University from January 2014 to December 2015 were included. Demographic characteristics including age and sex were collected at the beginning of the study.

The inclusion criteria were as follows: Patients aged >18 years; patients who were diagnosed with group B and C COPD in accordance with the Guidelines for the Diagnosis and Treatment of Chronic Obstructive Pulmonary Disease (revised edition from 2013), published by the COPD Group of the Chinese Thoracic Society (3); patients who received inhalation therapy; patients who did not receive any cholinolytic drugs within 4 weeks; patients who did not suffer from any acute attack and did not receive any antibiotic therapy for 4 weeks; patients who had not received any systemic glucocorticoid therapy in the past two months; patients who provided written informed consent. The exclusion criteria were as follows: Patients who were allergic to tiotropium bromide, budesonide/formoterol inhalation or any other inhaled ingredients; patients with diseases rendering them unsuitable for inhalation therapy, including bronchial lung cancer, dilatation and interstitial lung diseases; patients suffering from other systemic diseases, including heart, liver, kidney, hematopoietic and nervous system diseases, glaucoma or severe prostatic hyperplasia; patients who were considered unsuitable for participating in the drug trial by the clinicians.

Grouping and treatment

A total of 180 cases with moderate to severe COPD were randomly divided into a control group (positive drug controls) and an intervention group by using a random number table, with 90 cases in each group. Each of the two groups went through a 1-week washout period, after which they received treatment for 6 months. The control group received budesonide/formoterol (160/4.5 µg; 1 suction/time, 2 times/day; Symbicort Turbuhaler; AstraZeneca, Cambridge, UK). Based on the control group treatment, patients in the intervention group received additional treatment of tiotropium bromide (1.8 µg inhaled once a day before bed; Spiriva; C.H. Boehringer Sohn AG & Ko. KG, Ingelheim, Germany). During the study period, patients were provided with salbutamol inhalation on demand; antibiotics and antiviral drugs were used in specific cases if required.

Evaluation indices

The following indices were determined prior to treatment and after treatment for 3 and 6 months.

Lung function indices included the forced expiratory volume in 1 second (FEV1), the FEV1/forced vital capacity (FVC) and the FEV1 as a percentage of the predicted value (FEV1%pred).

Weight and height were measured for calculating the body mass index (BMI).

The dyspnea score was evaluated using the modified Medical Research Council (mMRC) scale (10). The scale included four grades, with a higher score indicating more serious dyspnea, ranging from 0 points-no breathing difficulties except during strenuous exercise, to 4 points-dyspnea when leaving the room, dressing or other light activities. The degrees of dyspnea were scored according to the patients' own description.

The six-minute walking test (6MWT) was performed by measuring the longest distance that patients were able to walk within 6 min while they were walking back and forth on corridor of 20 m in length (11). The test was performed twice with an interval time of at ≥2 h and the optimum value was recorded. This test was performed to assess the exercise tolerance of patients.

Health-associated quality of life was assessed using St. George's Respiratory Questionnaire (SGRQ) (12). SGRQ consisted of 50 items and three parts, assessing the influence of symptoms, ability to perform activities and disease on daily life, with a total score of 100 points. The score was negatively correlated with the health state. On the day of the pulmonary function test, the questionnaires were completed by the patients independently, and the researchers checked whether there was any omission.

During follow-up period, occurrence and time of acute exacerbation were recorded for the evaluation of acute attack risk and occurrence of mortality and adverse reactions were recorded for the evaluation of safety.

Statistical analysis

All data were processed using SPSS 20.0 (IBM Corp., Armonk, NY, USA). The measurement data were expressed as the mean ± standard deviation, and the difference in baseline measurement data between the two groups were compared with an independent-samples t-test. The difference test of categorical variables between the two groups was performed by using the two-tailed χ2 test or Fisher's exact probability test.

Comparisons of lung function, BMI, mMRC, 6MWT and SGRQ scores at different time-points, as well as differences in treatment effects of the two treatment methods at different time-points (interaction of treatment and time), were analyzed by repeated-measures analysis of variance (ANOVA). If the overall difference between the two groups in the repeated-measures ANOVA was significant, Bonferroni's post-hoc test (significance level set at 0.05/3=0.0167) was performed for the comparison of detection values or score at the same time-point. The risk of acute exacerbation since the start of treatment was compared between the groups by Kaplan-Meier survival analysis, with significant differences determined using the log-rank test. The days between first onset from the start of treatment exhibited a skewed distribution; therefore, the data were expressed as median (25 and 75% quartile) and the Mann-Whitney U-test was used for assessment of statistically significant differences. The study was analyzed in line with the Intent-To-Treat principle; for subjects that dropped out during the study, analysis was performed according to their last available data. The level of statistical significance was set as bilateral α=0.05 (except for Bonferroni's post-hoc test).

Results

General information

During the study period, 1 patient in the intervention group and 1 in control group dropped out due to of adverse reactions. The baseline and clinical characteristics of the patients in the two groups are presented in Table I. There was no significant difference in age, sex, smoking history, course of disease and degree of COPD between the two groups, indicating similar baseline and clinical data.

Table I.

General information on the patients in the two groups.

Characteristic	Intervention group (n=90)	Control group (n=90)	χ2/t	P-value
Age (years)	56.7±8.2	54.8±7.9	1.583	0.115
Sex			1.693	0.193
Male	67 (74.4)	59 (65.6)
Female	23 (25.6)	31 (34.4)
Smoking history			2.025	0.155
No	13 (14.4)	7 (7.8)
Yes	77 (85.6)	83 (92.2)
Course of disease (years)	11.6±5.7	10.3±5.1	1.612	0.109
COPD degree			1.105	0.293
B	47 (52.2)	54 (60.6)
C	43 (47.8)	36 (40.0)

Values are expressed as n (%) or the mean ± standard deviation. COPD, chronic obstructive pulmonary disease.

Co-treatment with tiotropium bromide significantly enhances the improvement of lung function in COPD patients receiving budesonide/formoterol

Table II presents the comparison of lung function between the two groups prior to treatment, and after treatment for 3 and 6 months. There was no significant difference in pulmonary function indices between the two groups prior to treatment. Repeated-measures ANOVA indicated that over the treatment time, the FEV1, FEV1/FVC (%) and FEV1%pred exhibited time-dependent increases in the groups (P=0.034, P=0.026 and P=0.020, respectively). Over the entire treatment duration, the differences in the above three indicators between the two groups were also significant (P=0.030, P=0.042 and P=0.038, respectively), and the improvement of lung function in the intervention group was significantly better than that in the control group. The FEV1 in the intervention group was significantly higher than that in the control group after treatment for 3 months (P=0.015) and 6 months (P=0.001); furthermore, at 6 months, the FEV1/FVC (%, P=0.006) and FEV1%pred (P=0.005) in the intervention group were significantly higher than those in the control group.

Table II.

Pulmonary function evaluation in the two groups.

				Difference between groups		Time effect		Group/time interaction[a]
Pulmonary function parameter	Prior to treatment	After 3 months treatment	After 6 months treatment	F	P-value	F	P-value	F	P-value
FEV1 (l)				4.783	0.030	3.417	0.034	3.253	0.040
Intervention group	1.10±0.35	1.40±0.42	1.46±0.45
Control group	1.14±0.39	1.25±0.40	1.25±0.41
t, P-value[b]	0.724, 0.470	2.453, 0.015	3.272, 0.001
FEV1/FVC (%)				4.209	0.042	3.672	0.026	2.342	0.098
Intervention group	54.34±9.30	58.52±9.79	62.01±9.10
Control group	53.27±8.67	56.02±8.36	58.28±8.71
t, P-value[b]	0.798, 0.426	1.842, 0.067	2.809, 0.006
FEV1%pred				4.357	0.038	3.944	0.020	0.571	0.565
Intervention group	52.32±6.67	55.89±7.08	59.02±7.24
Control group	52.17±7.67	53.75±7.15	55.93±7.45
t, P-value[b]	0.140, 0.889	2.017, 0.045	2.821, 0.005

‘Group/time interaction’ refers to the differences in the therapeutic effect of two treatments at different time-points, and was analysed by repeated-measures analysis of variance.

Difference between two groups determined by Bonferroni's post-hoc test (significance level, 0.05/3=0.0167). Values are expressed as the mean ± standard deviation. FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; FEV1%pred, FEV1 as percentage of predicted value.

Comparison of BMI, mMRC, 6MWT and SGRQ scores between the two groups during treatment

Similar to the results regarding pulmonary function, the BMI (P=0.044), mMRC score (P=0.017), 6MWT score (P=0.021) and SGRQ score (P=0.024) in the two groups improved significantly during treatment, suggesting that nutritional status, dyspnea, exercise endurance and quality of life in the two groups were significantly improved. The improvements of mMRC, 6MWT and SGRQ scores in the intervention group were significantly better than those in the control group (P=0.041, P=0.044 and P=0.034, respectively), but the difference in the BMI between the two groups was not statistically significant (P=0.302; Table III).

Table III.

Comparison of BMI, mMRC, 6MWT and SGRQ scores in the two groups.

				Difference between groups		Time effect		Group/time interaction[a]
Score	Prior to treatment	After 3 months treatment	After 6 months treatment	F	P-value	F	P-value	F	P-value
BMI (kg/m2)				1.072	0.302	3.142	0.044	1.282	0.279
Intervention group	21.2±2.7	21.9±2.8	22.4±3.2
Control group	20.9±2.6	21.6±3.0	22.0±2.9
mMRC score				4.233	0.041	4.110	0.017	0.469	0.626
Intervention group	3.02±0.46	2.45±0.31	1.53±0.26
Control group	3.05±0.53	2.67±0.36	1.85±0.29
t, P-value[b]	0.406, 0.686	4.393, 0.001	7.794, 0.001
6MWT (m)				4.091	0.044	3.926	0.021	2.149	0.118
Intervention group	283.9±42.65	322.8±48.89	331.92±49.87
Control group	279.5±40.09	309.77±47.15	314.23±47.29
t, P-value[b]	0.713, 0.477	1.820, 0.070	2.442, 0.016
SGRQ score				4.561	0.034	3.769	0.024	1.785	0.169
Intervention group	59.47±7.15	54.56±6.64	53.32±5.94
Control group	58.64±6.41	50.21±6.17	48.28±6.05
t, P-value[b]	0.820, 0.413	4.553, <0.001	5.639, <0.001

‘Group/time interaction’ refers to the differences in the therapeutic effect of two treatments at different time-points, and was analysed by repeated-measures analysis of variance.

Difference between two groups determined by Bonferroni's post-hoc test (significance level, 0.05/3=0.0167). Values are expressed as the mean ± standard deviation. BMI, body mass index; mMRC, modified Medical Research Council; 6MWT, six-minute walking test; SGRQ, St. George's Respiratory Questionnaire.

Effect of treatment on acute exacerbations

During the study, acute exacerbation in the intervention group and the control group occurred in 5 (5.6%) and 9 cases (10%), respectively. Survival analysis indicated that the difference in the risk of acute exacerbation between the two groups was not significant (log-rank test, P=0.238; Fig. 1). However, the median time to the first acute exacerbation from the start of the treatment in the intervention group was 53 days (25% quartile, 50 days; 75% quartile, 62 days), which was significantly longer than that in the control group (median, 37 days; 25% quartile, 23 days; 75% quartile, 39 days; Mann-Whitney U test, P=0.042) (Fig. 2).

Figure 1.

Risk of acute attack in the two groups. There was no significant difference in the risk of acute exacerbation between the two groups during the study (log rank test P=0.238). COPD, chronic obstructive pulmonary disease.

Figure 2.

Median time to the first exacerbation since the start of the treatment in the two groups. The median time to the first exacerbation in the intervention group (53 days; 25% quartile, 50 days; 75% quartile, 62 days) was significantly longer than that in the control group (37 days; 25% quartile, 23 days; 75% quartile, 39 days; P=0.042).

Adverse reactions

The incidence of adverse reactions in the intervention group and control group was 14.4 and 10.0%, respectively, and there was no significant difference in the rate of adverse reactions between the two groups. The major adverse reactions included dry mouth, pharynx discomfort, oral ulcer, dysuria and sinus arrhythmia (Table IV). Furthermore, 1 patient in the intervention group and 1 patient in the control group dropped out due to their perceived lack of a therapeutic effect. No mortalities occurred during study.

Table IV.

Adverse reactions in the two groups.

Adverse reactions	Intervention (n=90)	Control group (n=90)	χ2	P-value
No	77 (85.6)	81 (90.0)	0.829	0.363
Yes	13 (14.4)	9 (10.0)
Dry mouth	5 (5.6)	3 (3.3)		0.720[a]
Pharynx discomfort	2 (2.2)	2 (2.2)		1.000[a]
Oral ulcer	2 (2.2)	2 (2.2)		1.000[a]
Dysuria	2 (2.2)	2 (2.2)		1.000[a]
Sinus tachycardia	2 (2.2)	0 (0.0)		0.497[a]

Fisher's exact probability test. Values are expressed as n (%).

Discussion

Acute exacerbation of COPD is mainly caused by airway obstruction, which is triggered by chronic inflammation of the airways, lung parenchyma and blood vessels, resulting in a limitation of lung function and serious impairment of the quality of life of affected patients. However, a study has indicated that the level of inflammatory markers in patients with COPD in the stable phase remains higher than that in healthy individuals, suggesting that inflammation prevails in the stable phase (13). Therefore, the major treatment target in the stable phase COPD is to control inflammation, relieve symptoms, improve exercise tolerance and the health status, as well as to prevent acute exacerbation (14).

Tiotropium bromide is a novel cholinolytic bronchodilator, which dilates the bronchus through competing with acetylcholine and combining with the M1 and M3 receptors; the dissociation time with the M3 receptor is up to 35 h, resulting in long-lasting anti-cholinergic effects: After one administration, the dilation of the bronchus is maintained for ≥24 h. In addition, through competitive inhibition of the combination of acetylcholine and the M receptor, it suppresses inflammation and airway remodeling (15,16). The 4-year large-scale prospective randomized double-blinded placebo-controlled UPLIFT trial indicated that compared with placebo, tiotropium bromide continuously and effectively improved the lung function and quality of life of COPD patients, and reduced the risk of exacerbation and all-cause mortality; while it failed to improve the downward trend of the FEV1, subgroup analysis indicated that the decrease rate of FEV1 in young patients was significantly improved (17,18). A systematic evaluation, which compared tiotropium bromide with placebo, further confirmed these results (19). In addition, a study also demonstrated that tiotropium bromide and budesonide/formoterol had similar effects in the prevention of acute exacerbation (20).

Formoterol, as a highly selective long-acting β2 receptor agonist, improves airway obstruction and pulmonary function of COPD patients, relieves symptoms and increases the intake of glucocorticoid receptor/liposome complexes (21). Formoterol and tiotropium bromide further increase the bronchiectatic effect, but with a different mechanism (22). Furthermore, budesonide, an efficient local anti-inflammatory glucocorticoid, inhibits the production of inflammatory factors and the activity of inflammatory cells from multiple links, so as to improve airway inflammation, prevent airway remodeling and increase the number of cell membrane β2 receptor. Theoretically, tiotropium bromide, budesonide and formoterol should have synergistic effects (23). A study has indicated that compared with tiotropium bromide alone, the combination of tiotropium bromide and budesonide/formoterol more effectively improves pulmonary function, mMRC and 6MWT, reduces acute exacerbation and is also preferable due to its cost-effectiveness (24). Systematic reviews have indicated that the combination of the above three drugs obviously decreased the acute exacerbation of COPD, but their evaluation indices did not include lung function, nutritional status and exercise capacity, which ware of great significance in the evaluation of COPD; furthermore, the analysis suggested that budesonide and formoterol may be associated with an increased risk of pneumonia (25,26). Thus, the efficacy and safety of the combination of the three drugs should be further evaluated.

The results of the present study demonstrated that the lung function, mMRC, 6MWT and SGRQ scores were significantly improved in the two groups after treatment, but the improvements in the intervention group were more significant; however, the difference in the adverse reaction rates between the two groups was not significant. These results were similar to those of previous analogous studies, which indicated that compared with budesonide/formoterol alone, tiotropium bromide combined with budesonide/formoterol significantly improved indicators of COPD, including pulmonary function, quality of life and exercise capacity, but that adverse reactions were not significantly different from those in the budesonide/formoterol treatment group (21,27).

Previous studies have demonstrated that tiotropium bromide combined with budesonide/formoterol significantly reduced the risk of acute exacerbation in patients with COPD (28,29). In the present study, Kaplan-Meier analysis indicated that there was no significant difference in the risk of acute exacerbations between the two groups, which may be due to the patients' different state of COPD among the studies. In one study, COPD was complicated with respiratory failure in all subjects (29), while the subjects of the present study were patients with moderate to severe COPD, so the incidence of acute exacerbations in the short study period was relatively lower, and the difference in the risk of acute exacerbations between the two groups was not significant, which was similar to the results of another two studies on the combined application of tiotropium bromide with fluticasone/salmeterol (5,30). However, in the present study, the time to the first acute exacerbation from the start of the treatment in the intervention group was significantly longer compared with that in the control group. Thus, further evaluation is required to elucidate whether the combination of tiotropium bromide and budesonide/formoterol has a better efficacy in reducing the risk of acute exacerbation compared with budesonide/formoterol alone. The nutritional status in each of the two groups was significantly improved when compared with that prior to treatment, but the difference between the two groups was not significant, which was similar to the result of another study (27); possible reasons for the insignificant difference between the groups may be the short study period and the small sample size. In addition, the improvement of the quality of life in the intervention group was significantly greater than that in the control group, but according to a meta-analysis, the difference in the improvement of the SGRQ score between COPD patients treated with tiotropium bromide combined with budesonide/formoterol and those with tiotropium bromide alone was not statistically significant (8).

Of note, the present study had various shortcomings, including a small sample size, short-term evaluation of the efficacy and safety, and unavoidable bias from researchers and patients, as they were not blinded to the treatments. Therefore, the efficacy and long-term safety of tiotropium bromide combined with budesonide/formoterol requires further assessment in a randomized double-blinded controlled trial with a larger sample size.

In conclusion, the present study comprehensively evaluated the efficacy of inhalation therapy of tiotropium bromide combined with budesonide/formoterol in patients with moderate to severe COPD from the aspects of lung function, nutritional status, degree of dyspnea and exercise capacity. It was demonstrated that the combination of tiotropium bromide and budesonide/formoterol is significantly more efficacious than budesonide/formoterol alone with regard to various endpoints, including the improvement of lung function.