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Am J Respir Crit Care Med Vol 160. pp 1862–1868, 1999 ... Recherche de l'Hôpital Laval, Sainte-Foy, Québec, Canada; Department of Pulmonary/Immunology,.
Montelukast Added to Inhaled Beclomethasone in Treatment of Asthma MICHEL LAVIOLETTE, KERSTIN MALMSTROM, SUSAN LU, PAUL CHERVINSKY, JEAN-CLAUDE PUJET, IZABELLA PESZEK, JI ZHANG, and THEODORE F. REISS for the Montelukast/Beclomethasone Additivity Group Bronchology Unit, Centre de Recherche de l’Hôpital Laval, Sainte-Foy, Québec, Canada; Department of Pulmonary/Immunology, Statistics Program and Department of Biostatistics, Merck Research Laboratories, Rahway, New Jersey; New England Research Center, Inc., North Dartmouth, Massachusetts; and Centre de Diagnostic et de Réadaptation Respiratoire, Paris, France

The primary objective of this study was to determine whether montelukast, an oral leukotriene receptor antagonist, provides additional clinical benefit to the effect of inhaled corticosteroids. A total of 642 patients with chronic asthma (FEV1 50 to 85% of predicted value and at least a predefined level of asthma symptoms) incompletely controlled with inhaled beclomethasone, 200 mg twice daily using a spacer device, during the 4-wk run-in period were randomly allocated, in a double-blind, double-dummy manner to one of four treatment groups: (1) montelukast 10 mg plus continuing inhaled beclomethasone; (2) placebo tablet plus continuing inhaled beclomethasone; (3) montelukast 10 mg and inhaled placebo (after blind beclomethasone removal); and (4) placebo tablet and inhaled placebo (after blind beclomethasone removal). The primary endpoints were FEV1 and daytime asthma symptoms score. Montelukast provided significant (p , 0.05) clinical benefit in addition to inhaled beclomethasone by improving FEV1, daytime asthma symptom scores, and nocturnal awakenings. Blind removal of beclomethasone in the presence of placebo tablets caused worsening of asthma control, demonstrating that patients received clinical benefit from inhaled corticosteroids. Blind removal of beclomethasone in the presence of montelukast resulted in less asthma control but not to the level of the placebo group. All treatments were well tolerated; clinical and laboratory adverse experiences were generally similar to placebo treatment in this study. In conclusion, montelukast provided additional asthma control to patients benefitting from, but incompletely controlled on, inhaled beclomethasone. Laviolette M, Malmstrom K, Lu S, Chervinsky P, Pujet J-C, Peszek I, Zhang J, Reiss TF for the Montelukast/Beclomethasone Additivity Group. Montelukast added to inhaled beclomethasone in treatment of asthma. AM J RESPIR CRIT CARE MED 1999;160:1862–1868.

Recent asthma treatment guidelines define the goals of therapy: to achieve asthma control, i.e., near normal airway function, absence of asthma symptoms, no activity limitations, no episodes of worsening asthma, with an acceptable tolerability profile (1). However, many patients with persistent asthma cannot attain these treatment goals with a single controller medication even at high doses (2). Therefore, adding a second therapy with a complementary mechanism of action may provide more complete asthma control (2). Unfortunately, the use of multiple therapies complicates treatment regimens (3). For example, a previous report indicated that compliance with inhaled medications (30 to 60%) is less than with oral (70 to 80%) medications; multiple daily administration of any therapy also contributes to poor compliance (3). Therefore, an (Received in original form March 11, 1998 and in revised form June 1, 1999) Supported by a grant from Merck Research Laboratories. Correspondence and requests for reprints should be addressed to Theodore F. Reiss, M.D., Merck Research Laboratories, RY 33-648, P.O. Box 2000, Rahway, NJ 07065. E-mail: [email protected] Am J Respir Crit Care Med Vol 160. pp 1862–1868, 1999 Internet address: www.atsjournals.org

oral therapy administered once daily could potentially provide the clinical effectiveness desired in usual practice. Montelukast, a new, specific leukotriene receptor antagonist (4) provides clinical benefit to patients with chronic asthma with a once daily, oral administration (5, 6). Subgroup analysis in previous short-term studies with crossover designs suggested that montelukast could provide additional clinical benefit to patients using concomitant inhaled corticosteroids (7, 8). To prospectively determine whether concomitantly administered montelukast and inhaled corticosteroids cause additive clinical benefit, we performed a randomized, double-blind, double-dummy, clinical trial in patients with incompletely controlled asthma who were receiving inhaled beclomethasone 200 mg twice daily. At the time of random allocation, montelukast, 10 mg once daily at bedtime, was added to a treatment regiment of inhaled beclomethasone, 200 mg twice daily, and this treatment group was compared with a group of patients continuing this dose of inhaled beclomethasone alone. Blindly removing beclomethasone (switching to inhaled placebo in the presence of placebo tablets) determined whether patients enrolled in the trial benefitted clinically from inhaled corticosteroids. As a secondary objective, the study evaluated whether montelukast

Laviolette, Malmstrom, Lu, et al.: Montelukast/Beclomethasone in Asthma Control

could be substituted for inhaled beclomethasone by blindly switching patients from beclomethasone to montelukast.

METHODS This was a multicenter, randomized, parallel-group study consisting of a 4-wk, single-blind run-in period (Period 1) and a 16-wk, doubleblind treatment period (Period 2) with four treatment groups. The visits in Period 1 and the first two visits in Period 2 were separated by 2 wk; subsequent visits were separated by approximately 3 wk. The study was conducted at 70 study centers, in 18 countries in North America, Europe, Africa, Australia, and Asia. Written informed consent approved by the respective institutional review boards/ethical review committees and local regulatory agencies (where required) was obtained from each patient during or before the prestudy visit. Parental or guardian consent was obtained for patients younger than 18 yr of age.

Patients and Procedures Healthy, nonsmoking, male and female patients (age 15 yr and older), with a history of at least 1 yr of intermittent or persistent asthma symptoms treated with inhaled corticosteroids for at least 6 wk before the prestudy visit were eligible for participation (the dose of inhaled corticosteroid 1 wk before the prestudy visit was either equal or comparable to 400 to 500 mg of beclomethasone). Patients were excluded if they had respiratory disorders other than asthma or had signs and symptoms of an upper respiratory infection within 3 wk of the prestudy visit. Female patients had a negative pregnancy test at the prestudy visit. Antiasthma medications excluded before the prestudy visit were oral and parenteral corticosteroids within 1 mo; cromolyn and nedocromil within 2 wk; theophylline (oral and intravenous), b-agonists (oral or long-acting inhaled), and anticholinergic agents within 1 wk. Antihistamines, except terfenadine (within 2 wk) and astemizole (within 3 mo), were permitted as needed during the study; immunotherapy was allowed at a constant monthly dose if initiated at least 6 mo before the prestudy visit. Patients used short-acting, inhaled b-agonist on an “as needed” basis (via metered-dose inhalers of albuterol/salbutamol, 100 mg/actuation). During the run-in period (Period 1) patients were dispensed two inhalers (morning and evening), in a blind manner, containing beclomethasone (Beclovent; Allen & Hanburys, Research Triangle Park, NC; 50 mg/actuation) and a bottle of placebo tablets. Patients were instructed to take 4 puffs (200 mg twice daily) and a tablet once daily at bedtime. Inhaled study medication was administered with an AeroChamber spacer device (Forest Pharmaceuticals, St. Louis, MO) throughout the study. To be eligible for Period 2, patients were required to demonstrate, on at least two of the four visits in Period 1, an FEV1 between 50 and 85% of the predicted value after withholding inhaled b-agonist and antihistamine for at least 6 and 48 h, respectively, and to show at least a 15% increase in FEV1 (absolute value) 20 to 30 min after inhaled b-agonist administration. In addition, patients were required to have at least a minimum total daytime asthma symptom score (64 out of a possible 336 score) and daily average b-agonist use (as needed) of at least 1 puff during the last 2 wk of Period 1. Eligible patients were randomly allocated in a double-blind double-dummy manner (both montelukast and beclomethasone and their respective placebos were allocated in a double-blind manner) to one of four treatment groups according to a computer-generated schedule (with a blocking factor of 6, non-U.S. study sites; 8, U.S. study sites) to receive (1) montelukast 10 mg once daily and inhaled beclomethasone 200 mg twice daily (montelukast plus beclomethasone group); (2) placebo tablets once daily and inhaled beclomethasone 200 mg twice daily (beclomethasone group); (3) montelukast 10 mg once daily and inhaled placebo twice daily (after removal of beclomethasone) (montelukast group); or (4) placebo tablet once daily and inhaled placebo (after removal of beclomethasone) (placebo group). The latter two groups effectively received treatment for 12, rather than 16 wk because the removal of inhaled beclomethasone was performed blindly by replacing the morning and evening beclomethasone inhalers with placebo inhalers 2 and 4 wk, respectively, after randomization. Only patients at the

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U.S. study sites were enrolled in the fourth treatment arm (placebo group). Patient compliance was determined by weighing the beclomethasone/placebo canisters and by tablet counts (percent of tablets that should have been taken; percent of total weight that should have been used). Spirometry was collected at each clinic visit between 6:00 and 9:00 A.M. using a standard spirometer (Puritan Bennett PB100/PB110; Nellcor, Kansas City, KS); at least three spirometry maneuvers were performed and the highest FEV1 was recorded. The data were transmitted weekly to a spirometry quality control center for rigorous review of data quality (9) and adherence to spirometry inclusion criteria. Daily asthma symptoms score and nocturnal awakenings were recorded on a diary card using validated measurement scales (10). On the diary card, patients recorded their peak expiratory flow rate (PEFR), measured in the morning upon awakening and evening before evening dose of study medication, and daily as needed use of shortacting inhaled b-agonist. Physicians’ and patients’ global evaluations, using a seven-point scale (0 5 very much better, 6 5 very much worse) (6), and the self-administered Asthma Quality of Life Questionnaire (11) were also used. The diary card and patients’ questionnaires were translated from English to the appropriate local languages and adjusted for linguistic equivalence and cultural differences (12). FEV1 and patient-reported daytime asthma symptoms were the prespecified primary efficacy endpoints. Other prespecified endpoints were changes in daily, “as needed,” inhaled b-agonist use, morning and evening PEFR, nocturnal awakenings with asthma, and peripheral blood eosinophil counts. Prespecified asthma outcomes included percent days with asthma exacerbations and percent patients with asthma attacks. An asthma-exacerbation day was defined as a day when any one of the following occurred: a decrease of . 20% from baseline value in morning PEFR; PEFR , 180 L/min; an increase of . 70% from baseline value in b-agonist use (a minimum increase of two puffs); an increase . 50% from baseline in symptom score; “awake all night” with asthma; or worsening asthma requiring oral corticosteroid rescue, visit to a doctor’s office, or hospitalization. An asthma attack was defined as worsening asthma requiring an unscheduled visit, hospitalization, or treatment with oral corticosteroids (13). The safety and tolerability profile was determined by adverse experiences reports, physical examination, and 12-lead electrocardiography (ECG). Laboratory safety tests (including hematology, serum biochemistry, and urinalysis) and blood eosinophil counts were analyzed by a central laboratory (Covance Central Laboratory Services, Inc., Indianapolis, IN).

Statistical Analysis The prespecified primary comparison was between the additivity and beclomethasone groups. The placebo group was included to validate the clinical benefit from inhaled corticosteroid treatment; the comparison of the montelukast group with other treatment arms was a secondary objective and is described by means of summary statistics and confidence intervals (CI). Baseline values were calculated as the average of the last 2 wk of Period 1. The primary analysis for efficacy endpoints included all patients with either (if appropriate) a baseline and at least one treatment measurement. (All allocated patients were included in safety summaries.) Endpoints with baseline values were analyzed as change or percent change from baseline. All endpoints were calculated as average treatment period values over the 16 wk of Period 2 (comparison of the additivity and the beclomethasone groups) or over the last 10 wk of Period 2 (comparison of the montelukast and placebo groups with the beclomethasone group). The comparison over the last 10 wk of Period 2 was performed to allow time for the beclomethasone withdrawal groups to approach a clinical steady state. An analysis of variance (ANOVA) model was used to estimate treatment group means and betweengroup differences and to construct the 95% CI for the least-square (LS) means and the differences in LS means (14). The model contained factors for treatment and study center. Robust ANOVA was used and found to corroborate the primary analyses. The 7-point global evaluation score was analyzed by the ANOVA model; the scores were also collapsed into three categories—better (0, 1, 2), no change (3), and worse (4, 5, 6)—and analyzed with a Cochran-Mantel-Haens-

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TABLE 1 ALLOCATED PATIENTS’ BASELINE CHARACTERISTICS

Patients, n Age, yr* Duration of asthma, yr* Smoking history, pack-years* Sex, % male patients Race, % of patients White Hispanic Other† History of allergic rhinitis, % of patients History of exercise-induced asthma, % of patients FEV1, L‡ FEV1, % of predicted‡ Daytime symptoms, score‡ b-agonist use, puffs/d‡ Morning PEFR, L/min‡ Evening PEFR, L/min‡ Peripheral blood eosinophil counts, 103/ml‡

Placebo

Montelukast

Beclomethasone

Beclomethasone 1 Montelukast

48 41 (15–75) 17 (1–53) 0 (0–8) 40

201 38 (15–75) 17 (1–62) 0 (0–80) 49

200 39 (15–78) 18 (0.5–59) 0 (0–600) 52

193 40 (15–76) 19 (0.5–62) 0 (0–300) 56

83.3 4.2 12.5

94.0 2.5 3.5

92.0 0.5 7.5

91.7 3.1 5.2

90

74

74

76

77 2.5 6 0.7 71 6 11 2.4 6 0.7 4.2 6 3.0 407 6 73 419 6 71

89 2.6 6 0.7 72 6 12 2.1 6 0.8 3.5 6 2.3 420 6 92 433 6 92

83 2.5 6 0.7 71 6 12 2.2 6 0.8 3.5 6 2.5 403 6 86 416 6 82

88 2.6 6 0.7 72 6 12 2.2 6 0.8 3.4 6 2.2 412 6 91 431 6 92

0.23 6 0.20

0.23 6 0.19

0.22 6 0.18

0.22 6 0.18

* Median and range. † Includes Black, Asian, Indian, East Indian, Black/White, Hispanic/Black, Asian/White, Anglo-Chinese, and Mixed. ‡ Mean 6 SD.

zel (CMH) test to corroborate the ANOVA results (15). Fisher exact test was used to compare between-treatment group frequencies of asthma exacerbation and attacks, and adverse experiences. p Values were rounded to three decimal places; p < 0.05 was considered statistically significant. The study was designed to have 650 patients complete Period 2, 50 in the placebo and 200 in each of the other three treatment groups. This sample size allowed detection, with 95% power (at a 5 0.05; twosided test), of a 6.0 percentage point difference in FEV1 (percent change from baseline) and a 10.0% difference in daytime symptoms score (change from baseline) between the additivity and beclomethasone treatment groups.

RESULTS Patients

A total of 642 patients were randomly allocated: 193, 200, 201, and 48 to the montelukast plus beclomethasone, beclomethasone, montelukast, and placebo treatment, respectively. There were no clinically meaningful differences among the four treatment groups in any of the baseline characteristics (Table 1). A

summary of patients discontinued after randomization is given in Table 2. Additionally, data from five patients (daytime symptom scores) and six patients (FEV1) could not be included in the efficacy analysis because of the lack of baseline or treatment period values. Effects on Asthma Control Endpoints

Effects of adding montelukast to inhaled corticosteroids. The addition of montelukast (10 mg) to inhaled beclomethasone (200 mg twice daily) resulted in improved asthma control compared with beclomethasone alone, by demonstrating significant improvement in the primary and secondary endpoints (FEV1 [p , 0.001], daytime symptoms score [p 5 0.041]), morning PEFR (p 5 0.004), and nocturnal awakenings (p 5 0.027) over the 16-wk treatment period (Figure 1 and Table 3). Furthermore, the group receiving montelukast in addition to beclomethasone also experienced fewer days with asthma exacerbations (25% decrease) and fewer asthma attacks compared with patients receiving beclomethasone alone (Table 3).

TABLE 2 PATIENTS DISCONTINUED AFTER ALLOCATION

Randomized patients, n Discontinued, n Protocol deviation Withdrew consent Worsening asthma Other clinical adverse experiences Pregnancy Lost to follow-up

Placebo

Montelukast

Beclomethasone

Beclomethasone 1 Montelukast

48 11 0 3 7 0 1 0

201 42 5 10 23 4* 0 0

200 22 5 4 8 1† 2 2

193 16 1 8 2 4‡ 0 1

* Respiratory infection, upper respiratory infection, and gastritis. † Parkinsonism. ‡ Eczema, gastrointestinal disorder, hypertension, and influenza.

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Figure 1. Mean (6 SE) FEV1 mean percent change from baseline. Treatment groups: beclomethasone 1 montelukast (closed diamonds); beclomethasone (closed triangles); montelukast (closed circles); placebo (open squares). (See METHODS for explanation of treatment groups.) AM removal: morning beclomethasone inhaler was replaced with a placebo inhaler in the placebo and montelukast groups; PM removal: evening beclomethasone inhalers were replaced with placebo inhalers in placebo and montelukast groups.

from baseline value was 0.31 (0.08, 0.54) score for the placebo group compared with 20.09 (20.20, 0.02) score for the beclomethasone group. Similar changes on other endpoints, including b-agonist use (percent change) [placebo: 59.20% (25.77, 92.63); beclomethasone: 1.88% (13.79, 17.55)] and nocturnal awakenings (nights/week) [placebo: 0.44 (20.45, 1.33); beclomethasone: 20.8 (21.38, 20.36)] were observed. Comparison between montelukast and beclomethasone groups. The complete removal of beclomethasone also resulted in a decline in asthma control which did not reach the levels of the placebo group (Figure 1). The removal of both doses of beclomethasone resulted in a change in FEV1 of 25.31% (27.32, 23.30) for the montelukast group compared with 0.52% (21.48, 2.53) for the beclomethasone group. The removal of both doses of beclomethasone also affected other endpoints, e.g., daytime symptoms score which showed a mean change (95% CI) of 0.27 (0.17, 0.38) score for the montelukast group compared with 20.09 (20.20, 0.002) score for the beclomethasone group. In a post hoc analysis, the removal of just the morning dose of beclomethasone had little noticeable effect on the FEV1 compared with the same maneuver in the placebo group (Figure 1). Effect on Peripheral Blood Eosinophil Counts

Daily b-agonist use and the evening PEFR showed trends favoring concomitant therapy. The physicians’ global evaluations demonstrated significant improvements in the additivity group compared with beclomethasone (Table 3); 68.4, 25.3, and 6.3% of the patients in the additivity group felt better, experienced no change, or felt worse, respectively, compared with 54.1, 31.1, and 14.8% of the patients in the beclomethasone group (p 5 0.001 ANOVA and CMH test). Patients’ global evaluations showed qualitatively similar results, although the difference did not reach statistical significance (p 5 0.085) (Table 3). Comparison between placebo and beclomethasone groups. The complete blind removal of beclomethasone resulted in a decline of asthma control, e.g., FEV1 decreased over time (Figure 1); the mean percent change (95% CI) in FEV1 from baseline value was 211.96 (216.28, 7.64) for the placebo group compared with 0.52 (21.48, 2.53) for the beclomethasone group. The mean change (95% CI) in daytime symptom score

The baseline eosinophil counts were comparable in the four treatment groups (Table 1). Over the 16-wk treatment period, there was a significant increase in the eosinophil counts in the beclomethasone group compared with the additivity group (p 5 0.011) (Figure 2). Compliance

The compliance (mean 6 SD) with the inhaled study medication over the 16-wk treatment period was 96.5 6 19.4, 94.0 6 18.8, 92.4 6 18.7, and 94.6 6 16.3% for the placebo, montelukast, beclomethasone, and additivity groups, respectively. The compliance with oral medication was 99.0 6 0.7, 98.7 6 1.1, 98.7 6 0.7, and 98.6 6 1.7% for the placebo, montelukast, beclomethasone, and additivity groups, respectively. Safety Results

Clinical adverse experiences that occurred in at least 6% of patients in any of the four treatment groups are summarized

TABLE 3 ENDPOINTS: PRIMARY STUDY COMPARISON Beclomethasone 1 Montelukast* (n 5 193)

p Value†

0.72 (20.89, 2.33) 20.02 (20.02, 0.06) 20.02 (20.10, 0.06)

5.08 (3.43, 6.74) 0.14 (0.10, 0.18) 20.13 (20.22, 20.05)

, 0.001 , 0.001 0.041

6.04 (23.78, 15.86) 2.65 (21.31, 6.60) 1.81 (21.92, 5.55) 20.45 (20.85, 20.05) 17.92 (14.61, 21.23) 12.0 2.40 (2.20, 2.60) 1.86 (1.63, 2.10)

25.51 (215.54, 4.52) 10.41 (6.36, 14.47) 5.84 (2.00, 9.68) 21.04 (21.42, 20.67) 13.37 (9.97, 16.77) 6.2 1.95 (1.74, 2.16) 1.59 (1.35, 1.83)

Beclomethasone* (n 5 200) Primary Morning FEV1, %‡ Morning FEV1, L§ Daytime asthma symptoms score§ Other Total daily b-agonist use, %‡ Morning PEFR, L/min§ Evening PEFR, L/min§ Nocturnal awakenings, nights/wki Asthma exacerbations, % days Asthma attacks, % of patients Physicians’ global evaluation Patients’ global evaluation

* Least-square mean and the 95% CI. † Comparison of beclomethasone 1 montelukast with beclomethasone groups. ‡ Percentage change from baseline. § Change from baseline. i Includes nocturnal asthmatic patients only: beclomethasone, n 5 74; montelukast 1 beclomethasone, n 5 85.

0.08 0.0041 0.11 0.010 0.041 0.055 0.001 0.085

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in Table 4. The most commonly reported adverse experiences were upper respiratory tract infection, worsening asthma, and headache. Laboratory adverse experiences occurred with similar frequency across the four treatment groups. There were no patients who discontinued because of a laboratory abnormality. The incidence of elevated alanine aminotransaminase (ALT) and aspartame aminotransaminase (AST) were similar among the treatment groups; changes were generally transient and self-limited while continuing study medication.

DISCUSSION This study demonstrated that montelukast, 10 mg once daily, provided additional clinical benefit in patients incompletely controlled on a commonly used starting dose of inhaled beclomethasone (200 mg twice daily). The treatment effect was consistently observed across the clinical endpoints including measurement of airways obstruction, patient-reported endpoints, and worsening asthma episodes. Concomitant inhaled beclomethasone and montelukast therapy provided additive clinical benefit consistent with the in vivo effects of corticosteroids on leukotriene biosynthesis (16). Although in vitro studies have suggested that corticosteroids inhibit the production of the cysteinyl leukotrienes, in vivo studies in asthmatic patients have not demonstrated inhibiting effects. Specifically, cysteinyl leukotrienes can be recovered from the airways of asthmatic patients despite high-dose oral corticosteroid therapy (16); therefore, it is proposed that corticosteroids and leukotriene receptor antagonists may have complementary actions.

TABLE 4 MOST COMMON CLINICAL ADVERSE EXPERIENCES OCCURRING IN > 6% OF PATIENTS (% OF RANDOMLY ALLOCATED PATIENTS) Placebo (n 5 48)

Montelukast (n 5 201)

Beclomethasone (n 5 200)

Beclomethasone 1 Montelukast (n 5 193)

6.3 0 12.5 41.7 8.3 6.3 39.6 6.3 4.2 4.2 6.3

1.0 6.0 25.9 37.3 3.5 5.5 35.8 7.5 6.0 6.0 3.5

0.5 5.5 21.0 20.0 2.0 2.5 39.5 5.5 8.0 4.5 1.5

1.6 2.6 25.9 11.9 2.6 4.1 36.3 5.7 5.2 4.1 0.5

Percentage of patients per treatment group is reported.

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The conclusion that montelukast provided effects in addition to inhaled beclomethasone therapy was validated by demonstrating that the removal of inhaled beclomethasone (placebo group) caused worsening asthma control. The decrease in asthma control showed that patients enrolled in this study, although incompletely controlled, received clinical benefit from inhaled corticosteroid therapy. This prospective study also confirmed previous post hoc observations from previous trials, that leukotriene receptor antagonists provide additional clinical benefit to patients using constant doses of inhaled corticosteroids but with incomplete asthma control (5–8). Such additive clinical benefit of leukotriene receptor antagonists and inhaled corticosteroids has also been demonstrated in stable patients on high-dose inhaled corticosteroid therapy (17, 18). One of these trials (17) showed that inhaled corticosteroids can be tapered when a leukotriene receptor antagonist was given concomitantly. In addition to the complementary clinical benefit, we showed that the two therapies had additive effects on peripheral blood eosinophil counts. The eosinophil is believed to be an important effector inflammatory cell in asthma (19). A decrease in peripheral blood eosinophil counts has been observed previously with leukotriene receptor antagonists (20) and inhaled corticosteroids (21), as has decrease in airway eosinophils (22, 23). Although the mechanisms of these actions are not completely understood, it has been hypothesized that corticosteroids shorten eosinophil survival by increasing the rate of apoptosis (24), whereas leukotriene receptor antagonists may retard bone marrow eosinophil maturation by inhibiting synergistic effects of the cysteinyl leukotrienes with peptide growth factors on eosinophil/basophil stem cell maturation (25). In some clinical trials, adding a second agent including long-acting b-agonists (2, 26, 27) or theophylline (28, 29) has been shown to be more beneficial than doubling the dose of inhaled corticosteroids. Because increasing the dose of inhaled corticosteroids may not result in additional, clinically important benefit (30), the addition of another agent may be preferred (26, 27). Oral leukotriene receptor antagonists may play a role in this challenging patient population. Future headto-head studies will need to compare the relative merits of the different agents used concomitantly to achieve better asthma control. This study also suggested that the blind removal of inhaled beclomethasone from concomitant montelukast therapy resulted in loss of asthma control in some patients. If the dose of

Figure 2. Change from baseline values in peripheral blood eosinophil counts for each treatment group.

Asthenia/fatigue Nausea Headache Worsening asthma Bronchitis Cough Upper respiratory infection Influenza Pharyngitis Sinusitis Rash

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inhaled corticosteroids is to be lowered when administered concomitantly with a leukotriene receptor antagonist, it may make more clinical sense to slowly taper rather than rapidly remove this agent. An interesting post hoc observation from this study was the maintenance of the treatment effect in the montelukast group after the blind removal of half the 400-mg beclomethasone dose. (Figure 1, AM removal) Although 2 wk is probably insufficient to assess the long-term effects, it is interesting to hypothesize that a leukotriene receptor antagonist and a low, once daily dose of inhaled corticosteroids might provide similar asthma control as high doses of inhaled corticosteroids (providing less long-term exposure to inhaled corticosteroids). This hypothesis needs to be tested in specifically designed, prospective, clinical trials. In this trial, all study therapies were generally well tolerated; the frequencies of adverse events were comparable among all treatment groups (including placebo). Specifically, the combination of montelukast and inhaled beclomethasone was not associated with new clinical and laboratory adverse events. In conclusion, montelukast, a leukotriene receptor antagonist, provided additional asthma control to patients benefiting from, but incompletely controlled on inhaled beclomethasone. The combination of these agents provided both complementary and additive actions on peripheral blood eosinophils, a parameter of asthmatic inflammation. Acknowledgment : The authors thank Laura Fritsch for her coordination of the international part of the study, Beth C. Seidenberg, M.D., and Alan Nies, M.D., for their helpful discussions, and Reynold Spector, M.D., for his wisdom and scientific guidance.

10.

11.

12.

13.

14.

15. 16.

17.

18.

19.

20.

References 1. National Asthma Education and Prevention Program. 1997. Expert Panel Report II: Guidelines for the Diagnosis, and Management of Asthma. U.S. Department of Health and Human Services, National Institute of Health, Bethesda, MD. 2. Woolcock, A., B. Lundback, N. Ringdal, and L. A. Jacques. 1996. Comparison of additional of salmeterol to inhaled steroids with doubling of the dose of inhaled steroids. Am. J. Respir. Crit. Care Med. 153: 1481–1488. 3. Kelloway, J. S., R. A. Wyatt, and S. K. Adlis. 1994. Comparison of patients’ compliance with prescribed oral and inhaled asthma medications. Arch. Intern. Med. 154:1349–1352. 4. Jones, T. R., M. Labelle, M. Belley, E. Champion, L. Charette, J. Evans, A. W. Ford-Hutchinson, J. Y. Gauthier, A. Lord, P. Masson, M. McAuliffe, C. S. McFarlane, K. M. Metters, C. Pickett, H. Piechuta, I. W. Rodger, N. Sawywe, R. N. Young, R. Zamboni, and W. M. Abraham. 1995. Pharmacology of montelukast sodium (Singulair), a potent and selective leukotriene D4 receptor antagonist. Can. J. Physiol. Pharmacol. 73:191–201. 5. Altman, L. C., Z. Munk, J. Seltzer, N. Noonan, S. Shingo, J. Zhang, and T. F. Reiss for the Montelukast Asthma Study Group. 1998. A placebo-controlled, dose-ranging study of montelukast, a cysteinyl leukotriene-receptor antagonist. J. Allergy Clin. Immunol. 102:50–56. 6. Noonan, M. J., P. Chervinsky, M. Brandon, J. Zhang, S. Kundu, J. McBurney, and T. F. Reiss for the Montelukast Asthma Study Group. 1998. Montelukast, a potent leukotriene receptor antagonist, causes dose-related improvements in chronic asthma. Eur. Respir. J. 11:1232– 1239. 7. Reiss, T. F., C. A. Sorkness, W. Stricker, A. Botto, W. W. Busse, S. Kundu, and J. Zhang. 1997. Effects of montelukast (MK-0476), a potent cysteinyl leukotriene receptor antagonist, on bronchodilation in asthmatic subjects treated with and without inhaled corticosteroids. Thorax 52:45–48. 8. Reiss, T. F., L. C. Altman, P. Chervinsky, A. Bewtra, W. E. Stricker, G. P. Noonan, S. Kundu, and J. Zhang. 1996. Effects of montelukast (MK-0476), a new potent cysteinyl leukotriene (LTD 4) receptor antagonist, in patients with chronic asthma. J. Allergy Clin. Immunol. 98: 528–534. 9. Botto, A., K. Malmstrom, S. Lu, J. Zhang, and T. F. Reiss. 1997. Central-

21.

22.

23.

24. 25.

26.

27.

28.

29.

30.

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ized spirometry quality control lowers the variability in multicenter asthma clinical trials (abstract). Am. J. Respir. Crit. Care Med. 155:A893. Santanello, N. C., B. L. Barber, T. F. Reiss, B. S. Friedman, E. F. Juniper, and J. Zhang. 1997. Measurement characteristics of two asthma symptom diary scales for use in clinical trials. Eur. Respir. J. 10:646–651. Juniper, E. F., G. H. Guyatt, R. S. Epstein, P. J. Ferrie, R. Jaeschke, and T. K. Hiller. 1992. Evaluation of impairment of health related quality of life in asthma: development of a questionnaire for use in clinical trials. Thorax 47:76–83. Guillemin, F., C. Bombardier, and D. Beaton. 1993. Cross-cultural adaptation of health related quality of life measures: literature review and propose guidelines. J. Clin. Epidemiol. 46:1417–1432. Zhang, J., C. Song, and T. F. Reiss. 1997. Development and validation of a sensitive measure of worsening asthma (abstract). Am. J. Respir. Crit. Care Med. 155:A892. Dunnett, C. W., and A. C. Tamhane. 1992. Comparisons between a new drug and active and placebo controls in an efficacy clinical trial. Stat. Med. 11:1057–1063. Pocock, S. J., N. L. Geller, and A. A. Tsiatis. 1987. The analysis of multiple endpoints in clinical trials. Biometrics 43:487–498. Dworski, R., G. A. Fitzgerald, J. A. Oates, and J. R. Sheller. 1994. Effect of oral prednisone on airway inflammatory mediators in atopic asthma. Am. J. Respir. Crit. Care Med. 149:953–959. Löfdahl, C. G., T. F. Reiss, J. A. Leff, E. Israel, M. J. Noonan, A. F. Finn, B. C. Seidenberg, T. Capizzi, S. Kundu, and P. Godard. 1999. A leukotriene receptor antagonist, montelukast, allows tapering of inhaled corticosteriods while maintaining asthma control: a randomized, placebo controlled trial. B.M.J. 319:1–4. Tamaoki, J., M. Kondo, N. Sakai, J. Nakata, H. Takemura, A. Nagai, T. Takizawa, and K. Konno. 1997. Leukotriene antagonist prevents exacerbation of asthma during reduction of high-dose inhaled corticosteroid: the Tokyo Joshi-Idai Asthma Research Group. Am. J. Respir. Crit. Care Med. 155:1235–1240. Bousquet, J., P. Chanez, A. M. Vignola, J.-Y. Lacoste, and F. B. Michel. 1994. Eosinophil inflammation in asthma. Am. J. Respir. Crit. Care Med. 150:933–938. Reiss, T. F., P. Chervinsky, R. J. Dockhorn, S. Shingo, B. Seidenberg, and T. B. Edwards for the Montelukast Clinical Research Study Group. 1998. Montelukast, a once-daily leukotriene receptor antagonist, in the treatment of chronic asthma: a multicenter, randomized, double-blind trial. Arch. Intern. Med. 158:1213–1220. Wempe, J. B., E. P. Tammeling, G. H. Koëter, L. Håkansson, P. Venge, and D. S. Postma. 1992. Blood eosinophil numbers and activity during 24 hours: effects of treatment with budesonide and bambuterol. J. Allergy Clin. Immunol. 90:757–765. Pizzichini, E., J. A. Leff, T. F. Reiss, L. Hendeles, L. P. Boulet, L. X. Wei, A. Efthimiadis, J. Zhang, and F. E. Hargreave. 1999. Montelukast reduces airway eosinophilic inflammation in asthma: a randomized, controlled trial. Eur. Respir. J. (In press) Djukanovic, R., S. Homeyard, C. Gratziou, J. Madden, A. Walls, S. Montefort, D. Peroni, R. Polosa, S. Holgate, and P. Howarth. 1997. The effect of treatment with oral corticosteroids on asthma symptoms and airway inflammation. Am. J. Respir. Crit. Care Med. 155:826–832. Fuller, R., M. Johnson, and A. Bye. 1995. Fluticasone propionate—an update on preclinical and clinical experience. Respir. Med. 89:3–18. Wickremasinghe, R. G., M. A. Kahn, and A. V. Hoffbrand. 1993. Do leukotrienes play a role in the regulation of proliferation of normal and leukemic hemopoietic cells? Prostaglandins Leukotr. Essent. Fatty Acids 48:123–126. Greening, A. P., P. W. Ind, M. Northfield, and G. Shaw. 1995. Added salmeterol versus higher-dose corticosteroid in asthma patients with symptoms on existing inhaled corticosteroid. Lancet 344:219–224. Pauwels, R. A., C.-G. Löfdahl, D. S. Postma, A. E. Tattersfield, P. O’Byrne, P. J. Barnes, and A. Ullman, for the Formoterol and Corticosteroids Establishing Therapy (FACET) International Study Group. 1997. Effect of inhaled formoterol and budesonide on exacerbations of asthma. N. Engl. J. Med. 337:1405–1411. Rivington, R. N., L. P. Boulet, J. Cote, H. Kreisman, D. I. Small, M. Alexander, A. Day, Z. Harsanyi, and A. C. Darke. 1995. Efficacy of Uniphyl, salbutamol, and their combination in asthmatic patients on high-dose inhaled steroids. Am. J. Respir. Crit. Care Med. 151:325–332. Evans, D. J., D. A. Taylor, O. Zetterstrom, K. F. Chung, B. J. O’Connor, and P. J. Barnes. 1997. A comparison of low-dose inhaled budesonide plus theophylline and high-dose inhaled budesonide for moderate asthma. N. Engl. J. Med. 337:1412–1418. Kamada, A. K., S. J. Szefler, R. J. Martin, H. A. Boushey, V. M. Chinchilli, J. M. Drazen, J. E. Fish, E. Israel, S. C. Lazarus, and R. F. Le-

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AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE manske. 1996. Issues in the use of inhaled glucocorticoids. Am. J. Respir. Crit. Care Med. 153:1739–1748.

APPENDIX The Montelukast Study Group for this protocol consisted of the following investigators: Leonard C. Altman, M.D., United States; José Antonio Basomba Riba, M.D., Spain; Richard Beasley, M.D., New Zealand; Allan B. Becker, M.D., Canada; William E. Berger, M.D., United States; Jonathan A. Bernstein, M.D., United States; Stephen P. Blackie, M.D., Canada; Otto Brändli, M.D., Switzerland; Mark G. Britton, M.D., United Kingdom; Peter M. A. Calverley, M.D., United Kingdom; Kenneth R. Chapman, M.D., Canada; Paul Chervinsky, M.D., United States; John J. Condemi, M.D., United States; Stavros H. Constantopoulos, M.D., Greece; Martin J. Conway, M.D., United States; Ronald Dahl, M.D., Denmark; James H. Day, M.D., Canada; Jaime Del Carpio, M.D., Canada; Michael A. Drouin, M.D., Canada; Pierre Ernst, M.D., Canada; J. Mark Fitzgerald, M.D., Canada; Stanley P. Galant, M.D., United States; Aloysius P.M. Greefhorst, M.D., Netherlands; Gary N. Gross, M.D., United States; William G. Harris, M.D., United States; Jaques Hébert, M.D., Canada; Arthur Helbling, M.D., Switzerland; Stephen T. Holgate, M.D.,

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United Kingdom; Louis Irving, M.D., Australia; Alan J. Knox, M.D., United Kingdom; Gert Kunkel, M.D., Germany; Craig F. LaForce, M.D., United States; Michel Laviolette, M.D., Canada; Tak H. Lee, M.D., United Kingdom; Thomas W. Littlejohn, III, M.D., United States; David William Moote, M.D., Canada; Michael J. Noonan, M.D., United States; Piyush Patel, M.D., Canada; Bruno N. Petersen, M.D., Denmark; Michael Plit, M.D., South Africa; Vlassios S. Polychronopoulos, M.D., Greece; Jean-Claude Pujet, M.D., France; Joan Reibman, M.D., United States; Paolo Renzi, M.D., Canada; Nils R. Ringdal, M.D., Norway; Robert N. Rivington, M.D., Canada; Abraham R. Rubinfeld, M.D., Australia; Richard E. Ruffin, M.D., Australia; Steven A. Sahn, M.D., United States; Jean-Marie R. Saint-Remy, M.D., Belgium; Eric J. Schenkel, M.D., United States; Allen T. Segal, M.D., United States; Kaspar Sertl, M.D., Austria; D. Loren Southern, M.D., United States; Donald F. Stark, M.D., Canada; William W. Storms, M.D., United States; Douglas R. Taylor, M.D., New Zealand; Ian K. Taylor, M.D., United Kingdom; Philip J. Thompson, M.D., Australia; George D. Trakopoulos, M.D., Greece; Norbert Vetter, M.D., Austria; Alan A. Wanderer, M.D., United States; Yee-Tang Wang, M.D., Singapore; Peter W. J. Wiers, M.D., Netherlands; John A. Winder, M.D., United States; Ashley A. Woodcock, M.D., United Kingdom.