Fixed-dose combination of enteric-coated naproxen and immediate-release esomeprazole has comparable efficacy to celecoxib for knee osteoarthritis: two randomized trials

被引:44
作者
Hochberg, Marc C. [1 ]
Fort, John G. [2 ]
Svensson, Ola [3 ]
Hwang, Clara [4 ]
Sostek, Mark [4 ]
机构
[1] Univ Maryland, Sch Med, Div Rheumatol & Clin Immunol, Baltimore, MD 21201 USA
[2] POZEN Inc, Chapel Hill, NC USA
[3] AstraZeneca, Sodertalje, Sweden
[4] AstraZeneca, Wilmington, DE USA
基金
美国国家卫生研究院;
关键词
COX inhibitors; Esomeprazole magnesium; Naproxen; Non-inferiority; Nonsteroidal anti-inflammatory drugs (NSAIDs); Osteoarthritis; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; CLINICAL-TRIAL; STANDING-COMMITTEE; TASK-FORCE; RISK; INHIBITORS; ROFECOXIB; ADHERENCE; PLACEBO; RECOMMENDATIONS;
D O I
10.1185/03007995.2011.580340
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective: To demonstrate that a fixed-dose combination of enteric-coated naproxen 500 mg and immediate-release esomeprazole magnesium 20 mg has comparable efficacy to celecoxib for knee osteoarthritis. Research design and methods: Two randomized, double-blind, parallel-group, placebo-controlled, multicenter phase III studies (PN400-307 and PN400-309) enrolled patients aged >= 50 years with symptomatic knee osteoarthritis. Following an osteoarthritis flare, patients received naproxen/esomeprazole magnesium twice daily, celecoxib 200 mg once daily, or placebo for 12 weeks. Clinical trial registration: NCT00664560 and NCT00665431. Main outcome measures: Three co-primary efficacy endpoints were mean change from baseline to week 12 in Western Ontario and McMaster Osteoarthritis Index (WOMAC) pain and function subscales, and Patient Global Assessment of osteoarthritis using a visual analog scale (PGA-VAS). Results: In Study 307, 619 patients were randomized and 614 treated. In Study 309, 615 patients were randomized and 610 treated. Both naproxen/esomeprazole magnesium and celecoxib were associated with improvements (least squares mean change from baseline to week 12) in WOMAC pain (Study 307: -42.0 and -41.8, respectively; Study 309: -44.2 and -42.9, respectively), WOMAC function (Study 307: -36.4 and -36.3, respectively; Study 309: -38.9 and -36.8, respectively), and PGA-VAS (Study 307: 21.2 and 21.6, respectively; Study 309: 29.0 and 25.6, respectively). A prespecified non-inferiority margin of 10 mm between naproxen/esomeprazole magnesium and celecoxib was satisfied for each co-primary endpoint at week 12 in both studies. Significant improvements were observed with naproxen/esomeprazole magnesium versus placebo in both studies (p<0.05). Celecoxib was significantly different from placebo in Study 307 (p<0.05); however, the improvements were not significant in Study 309. Acetaminophen use and patient expectation of receiving active treatment (80% probability) may have contributed to a high placebo response observed. Conclusions: Naproxen/esomeprazole magnesium has comparable efficacy to celecoxib for the management of pain associated with osteoarthritis of the knee over 12 weeks.
引用
收藏
页码:1243 / 1253
页数:11
相关论文
共 47 条
[1]
National adherence to evidence-based guidelines for the prescription of nonsteroidal anti-inflammatory drugs [J].
Abraham, NS ;
El-Serag, HB ;
Johnson, ML ;
Hartman, C ;
Richardson, P ;
Ray, WA ;
Smalley, W .
GASTROENTEROLOGY, 2005, 129 (04) :1171-1178
[2]
DEVELOPMENT OF CRITERIA FOR THE CLASSIFICATION AND REPORTING OF OSTEOARTHRITIS - CLASSIFICATION OF OSTEOARTHRITIS OF THE KNEE [J].
ALTMAN, R ;
ASCH, E ;
BLOCH, D ;
BOLE, G ;
BORENSTEIN, D ;
BRANDT, K ;
CHRISTY, W ;
COOKE, TD ;
GREENWALD, R ;
HOCHBERG, M ;
HOWELL, D ;
KAPLAN, D ;
KOOPMAN, W ;
LONGLEY, S ;
MANKIN, H ;
MCSHANE, DJ ;
MEDSGER, T ;
MEENAN, R ;
MIKKELSEN, W ;
MOSKOWITZ, R ;
MURPHY, W ;
ROTHSCHILD, B ;
SEGAL, M ;
SOKOLOFF, L ;
WOLFE, F .
ARTHRITIS AND RHEUMATISM, 1986, 29 (08) :1039-1049
[3]
Altman RD, 2000, ARTHRITIS RHEUM-US, V43, P1905
[4]
Use of nonsteroidal Antiinflammatory drugs an update for clinicians - A scientific statement from the American Heart Association [J].
Antman, Elliott M. ;
Bennett, Joel S. ;
Daugherty, Alan ;
Furberg, Curt ;
Roberts, Harold ;
Taubert, Kathryn A. .
CIRCULATION, 2007, 115 (12) :1634-1642
[5]
Bellamy N, 2002, J RHEUMATOL, V29, P2473
[6]
Treatment of osteoarthritis with celecoxib, a cyclooxygenase-2 inhibitor: A randomized controlled trial [J].
Bensen, WG ;
Fiechtner, JJ ;
McMillen, JI ;
Zhao, WW ;
Yu, SS ;
Woods, EM ;
Hubbard, RC ;
Isakson, PC ;
Verburg, KM ;
Geis, GS .
MAYO CLINIC PROCEEDINGS, 1999, 74 (11) :1095-1105
[7]
ACCF/ACG/AHA 2008 Expert Consensus Document on Reducing the Gastrointestinal Risks of Antiplatelet Therapy and NSAID Use A Report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents [J].
Bhatt, Deepak L. ;
Scheiman, James ;
Abraham, Neena S. ;
Antman, Elliott M. ;
Chan, Francis K. L. ;
Furberg, Curt D. ;
Johnson, David A. ;
Mahaffey, Kenneth W. ;
Quigley, Eamonn M. .
CIRCULATION, 2008, 118 (18) :1894-1909
[8]
Efficacy and safety of etoricoxib 30 mg and celecoxib 200 mg in the treatment of osteoarthritis in two identically designed, randomized, placebo-controlled, non-inferiority studies [J].
Bingham, C. O., III ;
Sebba, A. I. ;
Rubin, B. R. ;
Ruoff, G. E. ;
Kremer, J. ;
Bird, S. ;
Smugar, S. S. ;
Fitzgerald, B. J. ;
O'Brien, K. ;
Tershakovec, A. M. .
RHEUMATOLOGY, 2007, 46 (03) :496-507
[9]
Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. [J].
Bombardier, C ;
Laine, L ;
Reicin, A ;
Shapiro, D ;
Burgos-Vargas, R ;
Davis, B ;
Day, R ;
Ferraz, MB ;
Hawkey, CJ ;
Hochberg, MC ;
Kvien, TK ;
Schnitzer, TJ ;
Weaver, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (21) :1520-1528
[10]
Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial [J].
Bresalier, RS ;
Sandler, RS ;
Quan, H ;
Bolognese, JA ;
Oxenius, B ;
Horgan, K ;
Lines, C ;
Riddell, R ;
Morton, D ;
Lanas, A ;
Konstam, MA ;
Baron, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (11) :1092-1102