| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
1 Dept of Respiratory Diseases, Atrium Medical Centre, Heerlen, the Netherlands. 2 Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT, USA. 3 , Boehringer Ingelheim br, Alkmaar, the Netherlands
CORRESPONDENCE: J.A. van Noord, Dept of Respiratory Diseases, Atrium medisch centrum, Henri Dunantstraat 5, 6419 PC, HEERLEN, The Netherlands. Fax: 31 455767534. E-mail: longarts.om@wolmail.nl
Keywords: anticholinergic, chronic obstructive pulmonary disease, hyperinflation, ipratropium, spirometry, tiotropium
Received: April 20, 2001
Accepted October 18, 2001
 |
Abstract |
|---|
 TOP Abstract MethodsResultsDiscussionReferences |
|---|
Trough FEV1 following 8 days of tiotropium was 0.19 L (18%) above baseline. Approximately 90% of this increase was achieved within 24 h of the first dose (0.17 L, 16%). Trough FVC increased 0.67 L (27%) on test-day 8. Approximately 70% of the improvement was observed after two tiotropium doses (0.47 L, 19%). Achievement of FVC steady state was delayed compared to FEV1. Ipratropium performed typically with an onset of action within 30 min, a peak response between 1–2 h postdosing and a duration of action of 
4 h. It was concluded that forced expiratory volume in one second steady state with tiotropium is reached within 48 h, while continued improvements in forced vital capacity can be expected over or beyond the first week of therapy. The continued increases in forced vital capacity beyond 48 h suggests that maintenance bronchodilator therapy is required to achieve maximal changes in hyperinflation.
Tiotropium (Spiriva®) is a newly developed anticholinergic bronchodilator, which is structurally related to the quaternary ammonium compound ipratropium. In vitro studies of isolated guinea pig and human airway have shown that the drug has a very long duration of action and a unique kinetic selectivity for muscarinic (M)3 and M1 over M2-subtypes of the M receptor 1–3. In early clinical, single-dose studies in chronic obstructive pulmonary disease (COPD) and asthma it was found that tiotropium produced a bronchodilator effect that was sustained for at least 24 h 4–6. Recently published long-term studies demonstrated that 18 µg of tiotropium is a safe and effective bronchodilator, suitable for maintenance therapy in COPD with once-daily dosing 7–9. Statistically significant and clinically relevant increases in the forced expiratory volume in one second (FEV1) value before the next dose and 24 h after the previous dose, were evident at 1 week into therapy, which confirmed the long bronchodilating effect.
From a therapeutic standpoint it is relevant to know the onset of maximum bronchodilator response for a drug intended for maintenance therapy, i.e. its pharmacodynamic steady state. Therefore, the present study was performed in a subset of patients participating in an ipratropium-controlled long-term efficacy and safety study in COPD 8. Serial measurements of FEV1 and forced vital capacity (FVC) were conducted on the first 3 days as well as after 1 week of treatment in order to characterize the onset of pharmacodynamic steady state.
|
Methods |
|---|
|
TOPAbstractMethodsResultsDiscussionReferences |
|---|
65% pred 11 and FEV1/FVC <70%, to be 
40 yrs of age and to have a smoking history of at least 10 pack-yrs. Patients with a history of asthma, allergic rhinitis, atopy or an elevated total blood eosinophil count were excluded. In addition, patients with any of the following were excluded from the study: a significant disease other than COPD, a recent history of myocardial infarction, heart failure or cardiac arrhythmia requiring drug therapy, oxygen therapy, an upper respiratory tract infection in the 6 weeks prior to screening, a known hypersensitivity to anticholinergic drugs, known symptomatic prostatic hypertrophy, and narrow-angle glaucoma.
Study design
The trial was designed as a randomized, double-blind, double-dummy, parallel group study and was approved by the hospital Medical Ethics Committee. All patients gave written informed consent before any study procedure was undertaken. The 1-week treatment period was preceded by a run-in period of 2 weeks. The patients continued to take the permitted medication for their COPD in stable doses, which included inhaled steroids, oral steroids up to 10 mg·day–1 prednisone and mucolytics. Long-acting inhaled ß2-agonists, oral ß2-agonists and cromolyn sodium were not allowed for at least 1 month before the screening visit as well as throughout the study period. Anticholinergics were allowed during the run-in period, but were discontinued at the randomization visit. Patients were given open-label salbutamol to use as rescue medication. Patients were randomly assigned to receive either tiotropium 18 µg once-daily (Spiriva®) + ipratropium-matched placebo q.i.d. (two-thirds of the patients) or ipratropium 40 µg q.i.d. (Atrovent®) + tiotropium-matched placebo (one-third of the patients). Tiotropium was inhaled from the HandiHaler®, a dry-powder inhaler system 12, between 08:00–10:00 h. Ipratropium (two puffs of 20 µg) was inhaled from a pressurized metered-dose inhaler (pMDI) between 08:00–10:00 h, at lunch, dinner and before going to bed.
Measurements
Pulmonary function testing always started between 08:00–09:00 h. FEV1 and FVC were obtained 1 h prior to, and just before inhalation and at 0.5, 1, 2, 3, 4, 5 and 6 h after inhalation of the morning dose (one capsule and two puffs from the pMDI). While the sampling interval chosen was not optimal to identify the time of onset of action, the intervals chosen were a practical compromise of the need to perform repeated pulmonary function measurements in a COPD population. When the 6-h postdosing measurement was completed, the second daily dose from the pMDI (two puffs) was administered and pulmonary function testing was continued at 0.5, 1 and 2 h. These measurements were performed with a spirometer meeting ATS criteria 13. The highest values of FEV1 and FVC from three technically adequate measurements were retained. Short-acting ß2-agonists and inhaled steroids were withheld 12 h before the lung function test. None of the randomized patients were receiving theophylline. In conjunction with the spirometry, measurements of blood pressure and pulse rate were collected. The laboratory safety evaluation, an electrocardiogram recording and physical examination were performed after 3 months of treatment as part of the long-term study 8.
Statistical analysis
Baseline FEV1 was defined as the mean of the two FEV1 readings in the morning of the randomization visit before inhalation of the study drug. For the other test days, the mean of the two morning predose FEV1 values was defined as trough FEV1 (i.e. 23–24 h after the preceding dose of tiotropium or 8–9 h after the preceding dose of ipratropium). The trough FEV1 response was defined as the change from baseline to trough FEV1; this parameter was chosen as the primary efficacy end point in order to establish pharmacodynamic steady state. As an additional bronchodilator parameter the peak FEV1 response during the 6-h period after inhalation on the pulmonary function test days was examined. Analogous definitions were used for FVC-based parameters.
Only randomized patients with complete baseline data and data at the end of the first week were eligible for the efficacy analysis. Descriptive statistics were used to evaluate the baseline comparability of the two treatments groups and no formal statistical comparison of the treatment groups was made. Change from baseline was evaluated using a paired t-test for each treatment group. The onset of pharmacodynamic steady state was verified using a repeated measures analysis applied to the repeat measurements for each tiotropium patient taken on test-days 2, 3 and 8. Test-day was specified as a fixed effect and patient as a random effect. The model was fit using maximum likelihood with an unstructured covariance matrix for the repeated measures. The randomization list was generated using a validated internal software program. The randomized list was based on block sizes of three.
|
Results |
|---|
|
TOPAbstractMethodsResultsDiscussionReferences |
|---|
). On the second test-day one patient in the tiotropium group was withdrawn from the study because of an exacerbation of COPD. Two other patients in the tiotropium group were excluded from all efficacy analysis due to incomplete data in the 1-week observation period. The mean (sem) baseline FEV1 at the start of treatment period was 1.04 (0.09) L for the tiotropium group and 1.07 (0.12) L for the ipratropium group. The FEV1 time/response curves after inhalation of the morning doses of tiotropium and ipratropium on test-days 1, 2, 3 and 8 are shown in figure 1.
|
|
. Approximately 90% of the FEV1 improvement was achieved within 24 h after the first tiotropium dose. The repeated measures analysis showed no significant difference (p>0.05) among test-days 2, 3, and 8 for trough and peak response.
|
The mean (sem) baseline FVC was 2.49 (0.22) L for the tiotropium group and 2.68 (0.22) L for the ipratropium group. The time/response curves on the four test days are shown in figure 3. The trough and peak response in FVC for the two drugs are illustrated in figure 2
. Approximately 70% of the day 8 FVC trough response in the tiotropium group was seen on test-day 2, i.e. 24 h after the first dose. An additional increase was observed on test-day 3, while the peak effect was reached on day 8. The repeated measures analysis showed no significant difference (p>0.05) among test days for peak response. However, there was a significant difference (p<0.05) for trough response. Also, in the ipratropium group there was a small trough FVC response (day 8), which was of similar magnitude on test-days 2 and 3. However, as with tiotropium the trough response continued to improve from day 1–8.
|
|
Discussion |
|---|
|
TOPAbstractMethodsResultsDiscussionReferences |
|---|
This rapid steady state in the lung is not unexpected as the topical concentration following inhalation of 18 µg rapidly equilibrates with lung fluid and membrane-bound receptors in the lung tissue. These concentrations are high in relation to the affinity constant of tiotropium at M3-receptors and probably leads to saturation of >90% with the first dose 3. The rapid onset of pharmacodynamic steady state is in contrast to the achievement of steady state in plasma. Here, as with many long-acting agents, which achieve a long duration of action by long plasma half-lives, there is a slow linear accumulation in plasma with steady state achieved at very low levels (i.e. 5 pg·mL–1) by the second to third week of treatment. Thus, there is no chronic accumulation beyond this level as evidenced by steady plasma levels for several months 14.
While the FEV1 trough response reached pharmacodynamic steady state rapidly, the maximum FVC response appeared to lag behind improvement in FEV1 during the first week of therapy. In fact, continued improvement in FVC was observed at the last measurement (day 8). However, it is likely that FVC improvements with tiotropium plateau between day 3–8, as the report by van Noord et al. 8 indicates no significant difference between day 8–51 values. Of interest, a similar pattern of FEV1 and FVC changes was observed with ipratropium, although the magnitude of changes was clearly superior with tiotropium. The changes in FVC observed over 8 days with tiotropium are unlikely to be explained by slowly accumulating M3-receptor occupancy alone, given the observations seen with ipratropium. Hence such changes may reflect slow improvement of the ventilatory condition of the lung by permanent or longer patency of previously closed airways.
Recent data suggests that volume changes are more important for improving the patient's perception of breathlessness. O'Donnell et al. 15 has reported that changes in hyperinflation are significantly correlated to improvements in dyspnoea during exercise testing in patients with COPD. While other measures of static lung volume were not measured in the present study, the improvement in FVC most likely reflects improvements in hyperinflation. The gradual increase in FVC over many days is consistent with the clinical observations of improvements being a continuing process that may not be fully appreciated within the first few days of treatment with inhaled bronchodilators. Studies with other classes and formulations of agents would also be useful in understanding these observations.
Further implications relate to what constitutes a bronchodilator response in patients with COPD. The classic assessment of a "bronchodilator response" is an FEV1 improvement higher than a predefined threshold acutely seen with a short-acting inhaled ß-agonist, a test profiled primarily in patients with asthma. These data and the increased emphasis on objective monitoring of dyspnoea in clinical trials suggests that therapeutic decisions based on an acute ß-agonist response may not be the most appropriate test of a bronchodilator response in patients with COPD, and a negative acute test should not exclude a relevant clinical response. Therefore, bronchodilator studies in patients with COPD should consider specifying volume changes after several days to weeks as an important end point, in addition to changes in FEV1 after the first dose. These data suggest that simple spirometric testing during clinical studies after the first dose should not lead to definitive conclusions about a bronchodilator's benefits in COPD.
Future investigations may consider extending the period of observation to determine more precisely when FVC pharmacodynamic steady state occurs following tiotropium administered once-daily and assess whether the attainment of steady state is similar for other static lung volumes including slow vital capacity, residual volume, inspiratory capacity, functional residual capacity and total lung capacity. Furthermore, the sample size in the present study is insufficient to determine the influence of severity of disease on the time required to attain steady state. It is quite probable that the extent of differing time constants within the lung would influence the time required to reach a steady state lung volume following pharmacological intervention. Clinically, this phenomenon provides a rationale for prolonged trials of inhaled bronchodilators before conclusions of clinical benefit can be stated. It is possible that a longer trial might have allowed time for a similar long-term improvement in lung function with ipratropium 16. A recent 12-week trial with salmeterol in patients with COPD did also indicate progressive improvements in morning predose FEV1 and FVC after 4 weeks of treatment 17.
To conclude, once-daily tiotropium provides sustained bronchodilation over 24 h with rapid improvements in spirometric measurements. The majority of bronchodilation is achieved with one to two doses; however continued improvements in lung volumes may be expected over or even beyond the first week of therapy.
|
References |
|---|
|
TOPAbstractMethodsResultsDiscussionReferences |
|---|
This article has been cited by other articles:
|
|
 |
|
  H. A. M. Kerstjens, T. A. Bantje, P. B. Luursema, H. E. J. Sinninghe Damste, J. W. de Jong, A. Lee, S. P. C. Wijker, and P. J. G. Cornelissen Effects of Short-Acting Bronchodilators Added to Maintenance Tiotropium Therapy Chest, November 1, 2007; 132(5): 1493 - 1499. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. Brand, T. Meyer, T. Weuthen, W. Timmer, E. Berkel, G. Wallenstein, and G. Scheuch Lung Deposition of Radiolabeled Tiotropium in Healthy Subjects and Patients With Chronic Obstructive Pulmonary Disease J. Clin. Pharmacol., October 1, 2007; 47(10): 1335 - 1341. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 R G Barr, J Bourbeau, C A Camargo, and F S F Ram Tiotropium for stable chronic obstructive pulmonary disease: a meta-analysis Thorax, October 1, 2006; 61(10): 854 - 862. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 K. E. Belmonte Cholinergic Pathways in the Lungs and Anticholinergic Therapy for Chronic Obstructive Pulmonary Disease Proceedings of the ATS, November 1, 2005; 2(4): 297 - 304. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 W. Vincken Bronchodilator treatment of stable COPD: long-acting anticholinergics Eur. Respir. Rev., September 1, 2005; 14(94): 23 - 31. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 H. Somand and T. L Remington Tiotropium: A Bronchodilator for Chronic Obstructive Pulmonary Disease Ann. Pharmacother., September 1, 2005; 39(9): 1467 - 1475. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. A. van Noord, J-L. Aumann, E. Janssens, J. J. Smeets, J. Verhaert, B. Disse, A. Mueller, and P. J. G. Cornelissen Comparison of tiotropium once daily, formoterol twice daily and both combined once daily in patients with COPD Eur. Respir. J., August 1, 2005; 26(2): 214 - 222. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
N. J. Gross Tiotropium Bromide Chest, December 1, 2004; 126(6): 1946 - 1953. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. F. Donohue Therapeutic Responses in Asthma and COPD: Bronchodilators Chest, August 1, 2004; 126(2_suppl_1): 125S - 137S. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D.E. O'Donnell, T. Fluge, F. Gerken, A. Hamilton, K. Webb, B. Aguilaniu, B. Make, and H. Magnussen Effects of tiotropium on lung hyperinflation, dyspnoea and exercise tolerance in COPD Eur. Respir. J., June 1, 2004; 23(6): 832 - 840. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. Turck, W. Weber, R. Sigmund, K. Budde, H.-H. Neumayer, L. Fritsche, K.-L. Rominger, U. Feifel, and T. Slowinski Pharmacokinetics of Intravenous, Single-Dose Tiotropium in Subjects with Different Degrees of Renal Impairment J. Clin. Pharmacol., February 1, 2004; 44(2): 163 - 172. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 {blacktriangledown}Tiotropium for chronic obstructive pulmonary disease DTB, February 1, 2003; 41(2): 15 - 16. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
: day 1; 
: day 2; 
: day 3; 
: day 8.
