Efficacy of Tiotropium + Olodaterol in Patients with Chronic Obstructive Pulmonary Disease by Initial Disease Severity and Treatment Intensity: A Post Hoc Analysis
verfasst von:
Gary T. Ferguson, Matjaž Fležar, Stephanie Korn, Lawrence Korducki, Lars Grönke, Roger Abrahams, Roland Buhl
The once-daily long-acting muscarinic antagonist (LAMA) tiotropium and once-daily long-acting β2-agonist (LABA) olodaterol have been studied as a once-daily fixed-dose combination (FDC) in patients with chronic obstructive pulmonary disease (COPD). Two large, 52-week, double-blind, parallel-group studies in patients with moderate–very severe COPD demonstrated that tiotropium + olodaterol significantly improved lung function and symptoms versus the monocomponents. This post hoc analysis determined effects on lung function by prior LAMA or LABA maintenance treatment and initial disease severity.
Methods
5162 patients were randomized and treated with olodaterol 5 µg, tiotropium 2.5 µg, tiotropium 5 µg, tiotropium + olodaterol 2.5/5 µg, or tiotropium + olodaterol 5/5 µg (all once daily via Respimat® inhaler). Primary efficacy (lung-function) end points were forced expiratory volume in 1 s (FEV1) area under the curve from 0 to 3 h (AUC0–3) and trough FEV1 responses (i.e., change from baseline). Pooled data are presented for the following subgroups: prior maintenance treatment with LAMA or LABA, Global initiative for chronic Obstructive Lung Disease (GOLD) 2 (predicted FEV1 50% to <80%) and 3 (30% to <50%)/4 (<30%), sex, age, and prior use of inhaled corticosteroids.
Results
Tiotropium + olodaterol FDC improved lung function over the monocomponents in patients with GOLD 2 and 3–4 disease, irrespective of prior LAMA or LABA maintenance therapy; most comparisons between FDCs and their respective monocomponents were statistically significant (P < 0.05). FEV1 AUC0–3 and trough FEV1 responses for the individual treatments were generally greater in patients with less severe COPD at baseline.
Conclusions
Tiotropium + olodaterol 5/5 µg significantly improved FEV1 AUC0–3 and trough FEV1 in all GOLD severity groups compared to olodaterol 5 µg and tiotropium 5 µg alone, irrespective of whether patients had received prior LAMA or LABA maintenance treatment. Improvements from baseline in lung function were generally greater in patients with less severe disease.
Funding
Boehringer Ingelheim.
Trial registration: ClinicalTrials.gov numbers, NCT01431274 and NCT01431287.
The online version of this article (doi:10.1007/s12325-015-0218-0) contains supplementary material, which is available to authorized users.
Introduction
Bronchodilators, including long-acting muscarinic antagonists (LAMAs) and long-acting β2-agonists (LABAs), are central to the maintenance treatment of patients with moderate to very severe chronic obstructive pulmonary disease (COPD) [1]. The once-daily LAMA tiotropium is well established in the treatment of COPD and improves the main functional and patient-orientated outcomes of the disease [2‐7]. Olodaterol is a novel once-daily LABA that provides 24-h bronchodilation [8‐11], symptomatic benefit [12], and enhanced exercise capacity [13]. Tiotropium + olodaterol has recently been evaluated in a phase III program to determine its efficacy in the treatment of COPD [14, 15].
International guidelines indicate that combining bronchodilators of different pharmacologic classes may improve efficacy and reduce the risk of side effects, rather than increasing the dose of a single bronchodilator. The introduction of combination products raises questions regarding the timing of their initiation during the course of COPD, with recent data indicating the potential benefits of earlier pharmacologic intervention with combination bronchodilator medications [16‐20].
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The pivotal phase III trials TONADO-1 and -2 have demonstrated that once-daily tiotropium + olodaterol significantly improved lung function and health-related quality of life compared to the monocomponents over 1 year in patients with moderate to very severe COPD [14]. These studies were notable in that they included a higher proportion of patients with more severe disease (Global initiative for chronic Obstructive Lung Disease [GOLD] 3 and 4) compared to previously reported studies of other LAMA and LABA combinations such as indacaterol + glycopyrronium [21, 22], and thus studied a broader population with respect to disease severity.
While significant responses were observed in the overall population of TONADO, evaluating the effectiveness of tiotropium + olodaterol in specific subgroups of patients is of clear interest to help inform health care providers. This is particularly pertinent in light of the fact that in clinical practice the population of patients with COPD is heterogeneous with respect to factors such as severity of disease, age, and concurrent COPD medication usage. The large nature of the TONADO studies offers the opportunity to study such subgroups. This post hoc analysis of the efficacy data from TONADO-1 and -2 was conducted to help understand these points, considering the effectiveness of tiotropium + olodaterol across COPD disease severities, in patients with or without prior bronchodilator or inhaled corticosteroid (ICS) use, and according to patients’ age and sex. As this analysis is post hoc, all P values and confidence intervals are nominal.
Methods
Study Design
Two replicate, multinational, phase III, randomized, double-blind, active-controlled trials were conducted to evaluate the efficacy and safety of tiotropium + olodaterol in comparison to the monotherapy components (TONADO-1, Study 1237.5: NCT01431274; TONADO-2, Study 1237.6: NCT01431287) (Fig. 1).
Fig. 1
Study design (Study 1237.5: NCT01431274; Study 1237.6: NCT01431287). R randomization, FDC fixed-dose combination, QD once daily
×
After a screening visit and 2-week baseline period, patients were randomized to receive tiotropium + olodaterol (2.5/5 or 5/5 μg) or the individual components as monotherapy (tiotropium 2.5 or 5 μg, or olodaterol 5 μg) via the Respimat® Soft Mist™ inhaler (Boehringer Ingelheim, Ingelheim am Rhein, Germany) for 52 weeks. Due to the length of therapy and the severity of disease studied, placebo was not used as a treatment arm in these studies. Patients receiving ICS at the start of the study could continue with their medication and all patients were provided with salbutamol/albuterol metered-dose inhaler (100 μg per actuation) as rescue medication, as required during the trial. Patients receiving a LAMA or LABA prior to the study were required to discontinue these medications during screening. The studies included outpatients aged ≥40 years with a history of moderate to very severe COPD (GOLD 2–4). Key inclusion and exclusion criteria are detailed in Fig. 2.
Fig. 2
Key inclusion and exclusion criteria. COPD chronic obstructive pulmonary disease, GOLD Global initiative for chronic Obstructive Lung Disease, FEV1 forced expiratory volume in 1 s
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End Points
The primary spirometry end points were evaluated after 24 weeks of treatment as follows: forced expiratory volume in 1 s (FEV1) area under the curve from 0 to 3 h (AUC0–3) and trough FEV1 responses (i.e., change from baseline to 24 weeks). Details of all assessments performed, end points evaluated, statistical methodology, and primary results for these studies have been reported previously [14].
Statistical Methods
In this analysis, FEV1 AUC0–3 and trough FEV1 were evaluated according to the following subgroups: patients without prior LAMA or LABA treatment at baseline or patients with prior LAMA or LABA treatment at baseline. Within each category of prior LAMA/LABA use, analyses were split according to whether patients had GOLD 2 (predicted FEV1 50% to <80%) or GOLD 3 (30% to <50%)/4 (<30%) COPD at baseline.
Pooled data from TONADO-1 and -2 were used in this analysis. Mean changes from baseline to 24 weeks were analyzed using a mixed-effect model repeated measures approach, including the fixed, categorical effects of treatment, test day, and treatment-by-test-day interaction, as well as the continuous, fixed covariates of baseline and baseline-by-test-day interaction. A spatial power covariance structure was used to model within-patient errors. The Kenward–Roger approximation was used to estimate denominator degrees of freedom.
In addition, pooled FEV1 AUC0–3 and trough FEV1 responses at 24 weeks were analyzed according to patients’ age (<65, 65 to <75, and 75 to <85 years), sex, and ICS usage using the model described above. These data are presented as forest plots, generated with SAS Version 9.2 (SAS Institute Inc., Cary, NC, USA).
Compliance with Ethics Guidelines
This article does not contain any new studies with human or animal subjects performed by any of the authors.
Results
Patient Disposition and Baseline Characteristics
A total of 5163 patients were randomized, of whom 5162 received study treatment (2624 Study 1237.5; 2538 Study 1237.6). The baseline characteristics of patients are presented in Tables 1 and 2 based on prior LAMA or LABA maintenance treatment for COPD and GOLD stage.
Table 1
Demographic and baseline patient characteristics (treated population): combined data for patients without prior LAMA or LABA treatment at baseline, stratified by initial GOLD stagea
Olodaterol 5 µg
Tiotropium 2.5 µg
Tiotropium 5 µg
Tiotropium + olodaterol 2.5/5 µg
Tiotropium + olodaterol 5/5 µg
GOLD 2 (n = 1148)
Participants, n
238
231
240
211
228
Male, n (%)
171 (71.8)
161 (69.7)
160 (66.7)
156 (73.9)
148 (64.9)
Mean (SD) age, years
63.6 (8.5)
63.2 (8.9)
62.5 (8.9)
64.4 (8.2)
63.0 (8.2)
Current smoker, n (%)
107 (45.0)
116 (50.2)
112 (46.7)
88 (41.7)
111 (48.7)
Post-bronchodilator screening
Mean (SD) FEV1, mL
1773 (483)
1785 (478)
1765 (474)
1769 (441)
1716 (435)
Mean (SD) change from pre- to post-bronchodilator FEV1, mL
172 (174)
210 (188)
184 (163)
202 (160)
175 (156)
Mean (SD) FEV1/FVC, %
52.6 (8.5)
52.7 (8.6)
54.5 (8.7)
53.0 (8.8)
54.2 (8.7)
Mean (SD) % of predicted normal FEV1
63.4 (8.2)
63.5 (8.1)
63.1 (8.4)
63.9 (8.3)
63.2 (8.8)
GOLD 3–4 (n = 973)
Participants, n
179
199
213
184
198
Male, n (%)
144 (80.4)
161 (80.9)
178 (83.6)
142 (77.2)
143 (72.2)
Mean (SD) age, years
63.0 (7.8)
62.3 (8.1)
62.7 (8.7)
63.1 (7.4)
62.4 (8.4)
Current smoker, n (%)
82 (45.8)
78 (39.2)
63 (29.6)
77 (41.8)
74 (37.4)
Post-bronchodilator screening
Mean (SD) FEV1, mL
1010 (292)
1022 (291)
1047 (286)
1052 (314)
996 (284)
Mean (SD) change from pre- to post-bronchodilator FEV1, mL
145 (116)
140 (136)
145 (118)
157 (111)
139 (163)
Mean (SD) FEV1/FVC, %
37.9 (9.3)
37.3 (9.6)
38.3 (10.3)
37.3 (8.6)
39.2 (10.2)
Mean (SD) % of predicted normal FEV1
36.5 (8.8)
36.4 (8.5)
36.8 (8.5)
37.5 (8.8)
36.4 (8.6)
LAMA long-acting muscarinic antagonists, LABA long-acting β2-agonist, GOLD Global initiative for chronic Obstructive Lung Disease, SD standard deviation, FEV1 forced expiratory volume in 1 s, FVC forced vital capacity
a Based on post-bronchodilator FEV1 percentage predicted
Table 2
Demographic and baseline patient characteristics (treated population): combined data for patients with prior LAMA or LABA at baseline, stratified by initial GOLD stagea
Olodaterol 5 µg
Tiotropium 2.5 µg
Tiotropium 5 µg
Tiotropium + olodaterol 2.5/5 µg
Tiotropium + olodaterol 5/5 µg
GOLD 2 (n = 1140)
Participants, n
294
287
277
308
274
Male, n (%)
201 (68.4)
202 (70.4)
180 (65.0)
210 (68.2)
202 (73.7)
Mean (SD) age, years
65.4 (8.0)
65.3 (9.1)
64.8 (8.7)
64.7 (8.2)
65.3 (8.9)
Current smoker, n (%)
87 (29.6)
102 (35.5)
98 (35.4)
107 (34.7)
98 (35.8)
Post-bronchodilator screening
Mean (SD) FEV1, mL
1693 (398)
1701 (401)
1685 (446)
1674 (409)
1690 (440)
Mean (SD) change from pre- to post-bronchodilator FEV1, mL
203 (144)
191 (144)
196 (170)
195 (151)
201 (151)
Mean (SD) FEV1/FVC, %
52.4 (8.5)
52.5 (8.4)
51.3 (8.7)
50.9 (9.2)
51.2 (8.7)
Mean (SD) % of predicted normal FEV1
62.9 (8.0)
62.2 (8.3)
62.7 (8.1)
61.6 (7.8)
62.0 (7.4)
GOLD 3–4 (n = 1597)
Participants, n
327
313
302
326
329
Male, n (%)
248 (75.8)
228 (72.8)
237 (78.5)
249 (76.4)
240 (72.9)
Mean (SD) age, years
64.3 (8.2)
64.5 (8.2)
64.9 (7.8)
64.0 (7.3)
64.0 (7.7)
Current smoker, n (%)
102 (31.2)
92 (29.4)
96 (31.8)
99 (30.4)
117 (35.6)
Post-bronchodilator screening
Mean (SD) FEV1, mL
1005 (288)
1057 (298)
993 (277)
1048 (295)
1008 (277)
Mean (SD) change from pre- to post-bronchodilator FEV1, mL
145 (124)
155 (122)
154 (120)
155 (118)
142 (120)
Mean (SD) FEV1/FVC, %
36.8 (8.6)
37.6 (8.8)
36.4 (8.7)
37.1 (8.8)
37.3 (8.8)
Mean (SD) % of predicted normal FEV1
36.8 (8.2)
38.3 (7.7)
36.2 (8.5)
37.8 (8.2)
37.0 (8.1)
LAMA long-acting muscarinic antagonists, LABA long-acting β2-agonist, GOLD Global initiative for chronic Obstructive Lung Disease, SD standard deviation, FEV1 forced expiratory volume in 1 s, FVC forced vital capacity
a Based on post-bronchodilator FEV1 percentage predicted
Overall baseline characteristics were similar across maintenance-treatment subgroups. Lung function in patients with GOLD 2 disease did tend to be slightly better in those who did not receive prior LAMA or LABA maintenance treatment than in those who received maintenance therapies before the study. In addition, more patients who received prior LAMA or LABA maintenance treatment were also taking ICS than those without prior maintenance treatment.
Efficacy
Patients Without Prior LAMA or LABA Maintenance Treatment
In each treatment group, FEV1 AUC0–3 responses (i.e., change from baseline) were greater in patients with GOLD 2 disease than GOLD 3–4 disease (Fig. 3a; Table S1 in the electronic supplementary material). In both of the GOLD subgroups, FEV1 AUC0–3 responses were greater with both doses of tiotropium + olodaterol than the monotherapy components at Week 24, and differences were statistically significant for all comparisons analyzed (Table 3).
Fig. 3
Adjusted mean FEV1 AUC0–3 responses at 24 weeks; pooled data from TONADO-1 and -2. a Patients without prior LAMA or LABA use; b patients with prior LAMA or LABA use. FEV1 forced expiratory volume in 1 s, AUC0–3 area under the curve from 0 to 3 h, LAMA long-acting muscarinic antagonist, LABA long-acting β2-agonist, SE standard error, O olodaterol, T tiotropium, GOLD Global initiative for chronic Obstructive Lung Disease
Table 3
Adjusted mean (SE) FEV1 AUC0–3 and trough FEV1 responses (i.e., change from baseline) after 24 weeks of treatment (full analysis set): combined data for patients without prior LAMA or LABA treatment at baseline: treatment differences
Treatment comparison
Adjusted mean (SE) FEV1 AUC0–3, mL
95% CI
P value
Adjusted mean (SE) trough FEV1, mL
95% CI
P value
GOLD 2
Tiotropium + olodaterol 5/5 µg
versus olodaterol 5 µg
127 (19)
90, 164
<0.0001
82 (20)
43, 120
<0.0001
versus tiotropium 5 µg
114 (19)
77, 151
<0.0001
79 (20)
40, 118
<0.0001
Tiotropium + olodaterol 2.5/5 µg
versus olodaterol 5 µg
98 (19)
61, 136
<0.0001
66 (20)
26, 105
0.0012
versus tiotropium 2.5 µg
108 (19)
70, 146
<0.0001
71 (20)
31, 111
0.0005
versus tiotropium 5 µg
85 (19)
47, 123
<0.0001
63 (20)
23, 102
0.0020
GOLD 3–4
Tiotropium + olodaterol 5/5 µg
versus olodaterol 5 µg
134 (19)
96, 171
<0.0001
92 (20)
53, 131
<0.0001
versus tiotropium 5 µg
114 (18)
79, 150
<0.0001
69 (19)
32, 106
0.0002
Tiotropium + olodaterol 2.5/5 µg
versus olodaterol 5 µg
120 (19)
82, 159
<0.0001
53 (20)
13, 92
0.0091
versus tiotropium 2.5 µg
117 (19)
80, 154
<0.0001
44 (20)
6, 83
0.0237
versus tiotropium 5 µg
101 (19)
65, 137
<0.0001
30 (19)
−8, 67
0.1237
Adjusted mean (SE) obtained from fitting a mixed model for repeated measurements including fixed effects of treatment, planned test day, treatment-by-test-day interaction, baseline, and baseline-by-test-day interaction; patient as a random effect; spatial power covariance structure for within-patient errors and Kenward–Roger approximation of denominator degrees of freedom
SE standard error, FEV1 forced expiratory volume in 1 s, AUC0–3 area under the curve from 0 to 3 h, LAMA long-acting muscarinic antagonist, LABA long-acting β2-agonist, CI confidence interval, GOLD Global initiative for chronic Obstructive Lung Disease
×
Trough FEV1 responses were consistently greater with both doses of tiotropium + olodaterol than the monotherapy components; no obvious trend was apparent between patients with GOLD 2 and GOLD 3–4 COPD (Fig. 4a). While all differences between the various monotherapies and tiotropium + olodaterol 5/5 µg were statistically significant in patients with GOLD 2 COPD, in GOLD 3–4 COPD patients receiving tiotropium + olodaterol 2.5/5 µg the differences were not as robust, such that changes in trough FEV1 with tiotropium 5 µg were not significantly different from tiotropium + olodaterol 2.5/5 µg (Table 3).
Fig. 4
Adjusted mean trough FEV1 responses at 24 weeks; pooled data from TONADO-1 and -2. a Patients without prior LAMA or LABA use; b patients with prior LAMA or LABA use. FEV1 forced expiratory volume in 1 s, LAMA long-acting muscarinic antagonist, LABA long-acting β2-agonist, SE standard error, O olodaterol, T tiotropium, GOLD Global initiative for chronic Obstructive Lung Disease
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Patients Receiving Prior LAMA or LABA Maintenance Treatment
In patients who received prior maintenance treatment, as in patients without prior LAMA or LABA maintenance bronchodilator therapy, the FEV1 AUC0–3 responses for the individual treatments were greater in those with less severe COPD (Fig. 3b; Table S2 in the electronic supplementary material). Again, FEV1 AUC0–3 responses were greater with both doses of tiotropium + olodaterol than the monotherapy components and all comparisons were statistically significant (P < 0.001).
Trough FEV1 responses were consistently greater with both doses of tiotropium + olodaterol than the monotherapy components and were generally greater in patients with less severe COPD (with the exception of tiotropium + olodaterol 2.5/5 µg) (Fig. 4b). All comparisons between tiotropium + olodaterol and the monotherapies were statistically significant in patients with GOLD 3–4 COPD; however, the comparisons between tiotropium + olodaterol 2.5/5 µg and tiotropium 2.5 or 5 µg in patients with GOLD 2 COPD did not achieve statistical significance (Table 4).
Table 4
Adjusted mean (SE) FEV1 AUC0–3 and trough FEV1 responses (i.e., change from baseline) after 24 weeks of treatment (full analysis set): combined data for patients with prior LAMA or LABA treatment at baseline: treatment differences
Treatment comparison
Adjusted mean (SE) FEV1 AUC0–3, mL
95% CI
P value
Adjusted mean (SE) trough FEV1, mL
95% CI
P value
GOLD 2
Tiotropium + olodaterol 5/5 µg
versus olodaterol 5 µg
136 (17)
102, 169
<0.0001
85 (18)
50, 121
<0.0001
versus tiotropium 5 µg
123 (17)
89, 157
<0.0001
61 (18)
26, 97
0.0007
Tiotropium + olodaterol 2.5/5 µg
versus olodaterol 5 µg
102 (17)
69, 135
<0.0001
43 (17)
9, 77
0.0133
versus tiotropium 2.5 µg
113 (17)
81, 146
<0.0001
25 (17)
−9, 59
0.1567
versus tiotropium 5 µg
89 (17)
56, 122
<0.0001
19 (18)
−16, 53
0.2830
GOLD 3–4
Tiotropium + olodaterol 5/5 µg
versus olodaterol 5 µg
119 (14)
92, 146
<0.0001
83 (13)
57, 109
<0.0001
versus tiotropium 5 µg
95 (14)
68, 122
<0.0001
41 (14)
15, 68
0.0023
Tiotropium + olodaterol 2.5/5 µg
versus olodaterol 5 µg
134 (14)
107, 162
<0.0001
85 (14)
58, 111
<0.0001
versus tiotropium 2.5 µg
107 (14)
80, 134
<0.0001
45 (14)
18, 71
0.0010
versus tiotropium 5 µg
110 (14)
83, 138
<0.0001
43 (14)
16, 70
0.0016
Adjusted mean (SE) obtained from fitting a mixed model for repeated measurements including fixed effects of treatment, planned test day, treatment-by-test-day interaction, baseline, and baseline-by-test-day interaction; patient as a random effect; spatial power covariance structure for within-patient errors and Kenward–Roger approximation of denominator degrees of freedom
SE standard error, FEV1 forced expiratory volume in 1 s, AUC0–3 area under the curve from 0–3 h, LAMA long-acting muscarinic antagonist, LABA long-acting β2-agonist, CI confidence interval, GOLD Global initiative for chronic Obstructive Lung Disease
Other Patient Subgroups
FEV1 AUC0–3 and trough FEV1 responses at 24 weeks are presented by age, sex, and prior ICS usage in Figs. 5 and 6. These show that tiotropium + olodaterol was more effective than the monotherapy components across all of the subgroups analyzed, with the exception of trough FEV1 (tiotropium + olodaterol 5/5 µg versus tiotropium 5 µg) in patients aged 75–85 years.
Fig. 5
Forest plots for FEV1 AUC0–3 responses at 24 weeks. a Tiotropium + olodaterol 5/5 µg versus olodaterol 5 µg; b tiotropium + olodaterol 5/5 µg versus tiotropium 5 µg. FEV1 forced expiratory volume in 1 s, AUC0–3 area under the curve from 0 to 3 h, ICS inhaled corticosteroid
Fig. 6
Forest plots for trough FEV1 responses at 24 weeks. a Tiotropium + olodaterol 5/5 µg versus olodaterol 5 µg; b tiotropium + olodaterol 5/5 µg versus tiotropium 5 µg. FEV1 forced expiratory volume in 1 s, ICS inhaled corticosteroid
×
×
Discussion
In all the patient subgroups included in this analysis of pooled data from the TONADO-1 and -2 studies, tiotropium + olodaterol consistently resulted in greater improvements in lung function than the monotherapy components, as determined by FEV1 AUC0–3 and trough FEV1 responses at 24 weeks. These results are in line with data from other studies using a LAMA and a LABA, and further highlight the benefits of combined bronchodilation over monotherapy treatment [23‐25]. Of particular note, tiotropium + olodaterol 5/5 µg once daily improved lung function in patients with GOLD 2 and 3–4 disease, and there were no apparently relevant differences in lung-function responses according to whether these patients had or had not received prior maintenance therapy with a LAMA or a LABA.
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While no statistical comparisons were made between subgroups, it was apparent that both FEV1 AUC0–3 and trough FEV1 responses for the individual treatments were, in general, greater in patients with less severe disease. The greater lung-function responses observed in patients with GOLD 2 COPD in our studies are in line with other clinical trials, including the 4-year study of tiotropium (UPLIFT; NCT00144339) [18]. While patients are less symptomatic earlier in their disease course, recent data have suggested that the progression of early COPD occurs at a faster rate than during the later stages of disease [16, 17]. In addition, the UPLIFT study suggested a possible reduction in the rate of decline of post-bronchodilator FEV1 in patients with GOLD 2 COPD using tiotropium [18]. As more information becomes available related to the response of symptoms, lung function, and exacerbations to good maintenance bronchodilator therapy in COPD patients with less severe disease, opinion is moving towards using effective bronchodilation in the earlier stages of COPD [18, 26].
Our data support the use of dual-action maintenance bronchodilator therapy with LAMA + LABA for treatment-naive and less severe COPD, as well as those more severe patients already receiving maintenance therapies. Both doses of tiotropium + olodaterol were more effective than the monotherapy components in all subgroups analyzed, although the lower dose of the combination (2.5/5 µg) may have been slightly less effective in providing trough bronchodilation in less severe, treatment-naive patients. In addition, it appeared that the FEV1 AUC0–3 responses were somewhat greater in younger patients than older patients, a finding that may reflect more the greater response in the less severe patients rather than a primary age effect. Otherwise, no major differences in responses were observed between treatment groups.
Our analysis does have some limitations in so far as it was post hoc and no direct statistical comparisons could be made between subgroups. However, based on the fact that data were pooled from two large phase III studies, the subgroups were all sizeable (each comprising >900 patients), allowing a clear evaluation of the effects of tiotropium + olodaterol in comparison to the monotherapy components.
Conclusions
Tiotropium + olodaterol 5/5 µg resulted in improved lung-function responses compared to the monotherapy components across all subgroups analyzed. These data show that tiotropium + olodaterol is effective in patients irrespective of age, disease severity, and prior treatment with bronchodilators and/or ICS.
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The improvements from baseline in lung function were greater in patients with less severe disease, adding support for the use of combination bronchodilation earlier in the course of COPD.
Acknowledgments
The authors received no compensation related to the development of the manuscript. This work, article processing charges and open access fee were supported by Boehringer Ingelheim Pharma GmbH & Co. KG. Medical writing assistance was provided by Rob Kite, on behalf of Complete HealthVizion, and was contracted and compensated by Boehringer Ingelheim Pharma GmbH & Co. KG. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this manuscript. They take full responsibility for the scope, direction, content of, and editorial decisions relating to, the manuscript, were involved at all stages of development, and have approved the submitted manuscript.
Conflict of interest
G.T. Ferguson has received grants, personal fees, and non-financial support from Boehringer Ingelheim and Forest, personal fees and non-financial support from GlaxoSmithKline, grants and personal fees from Novartis, AstraZeneca, and Pearl Therapeutics, and personal fees from Sunovion.
M. Fležar has received personal fees from Boehringer Ingelheim and institutional financial support from Novartis.
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S. Korn has received grants and personal fees from AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, Novartis, and Takeda, grants from Teva and MedImmune, and personal fees from Almirall and Grifols.
L. Korducki is an employee of Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, Connecticut, USA.
L. Grönke is an employee of Boehringer Ingelheim Pharma GmbH and Co. KG.
R. Abrahams has received grants and personal fees from Boehringer Ingelheim and GlaxoSmithKline, and grants from Forest, Pearl Therapeutics, and Pfizer.
R. Buhl has received grants and personal fees from Boehringer Ingelheim, Novartis, and Roche, and personal fees from AstraZeneca, Chiesei, Grifols, GlaxoSmithKline, and Takeda.
Compliance with ethics guidelines
Both studies were performed in accordance with the Declaration of Helsinki, International Conference on Harmonisation Harmonised Tripartite Guideline for Good Clinical Practice, and local regulations. The protocols were approved by the authorities and the ethics committees of the respective institutions, and signed informed consent was obtained from all patients.
This article does not contain any new studies with human or animal subjects performed by any of the authors.
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