Gastrointestinal Toxicity With Celecoxib vs Nonsteroidal Anti-inflammatory Drugs for Osteoarthritis and Rheumatoid Arthritis: The CLASS Study: A Randomized Controlled Trial

• Published in: JAMA : the journal of the American Medical Association Vol. 284; no. 10; pp. 1247 - 1255
• Main Authors: Silverstein, Fred E, Faich, Gerald, Goldstein, Jay L, Simon, Lee S, Pincus, Theodore, Whelton, Andrew, Makuch, Robert, Eisen, Glenn, Agrawal, Naurang M, Stenson, William F, Burr, Aimee M, Zhao, William W, Kent, Jeffrey D, Lefkowith, James B, Verburg, Kenneth M, Geis, G. Steven
• Format: Journal Article
• Language: English
• Published: Chicago, IL American Medical Association 13.09.2000
• Subjects: Arthritis; Biological and medical sciences; Drug toxicity and drugs side effects treatment; Drugs; Medical research; Medical sciences; Pharmacology. Drug treatments; Side effects; Toxicity; Toxicity: digestive system; Ulcers; Prostaglandin-endoperoxide synthase; Toxicity; Diseases of the osteoarticular system; Autoimmune disease; Inflammatory joint disease; Gastroduodenal; Intestinal disease; Ulcer; Degenerative disease; Gastric disease; Human; Immunopathology; Enzyme; Enzyme inhibitor; Celecoxib; Non steroidal antiinflammatory agent; Chemotherapy; Chronic; Treatment; Rheumatoid arthritis; Arthropathy; Digestive diseases; Oxidoreductases; Osteoarthritis; Comparative study
• ISSN: 0098-7484; 1538-3598
• DOI: 10.1001/jama.284.10.1247

CONTEXT Conventional nonsteroidal anti-inflammatory drugs (NSAIDs) are associated with a spectrum of toxic effects, notably gastrointestinal (GI) effects, because of inhibition of cyclooxygenase (COX)-1. Whether COX-2–specific inhibitors are associated with fewer clinical GI toxic effects is unknown. OBJECTIVE To determine whether celecoxib, a COX-2–specific inhibitor, is associated with a lower incidence of significant upper GI toxic effects and other adverse effects compared with conventional NSAIDs. DESIGN The Celecoxib Long-term Arthritis Safety Study (CLASS), a double-blind, randomized controlled trial conducted from September 1998 to March 2000. SETTING Three hundred eighty-six clinical sites in the United States and Canada. PARTICIPANTS A total of 8059 patients (≥18 years old) with osteoarthritis (OA) or rheumatoid arthritis (RA) were enrolled in the study, and 7968 received at least 1 dose of study drug. A total of 4573 patients (57%) received treatment for 6 months. INTERVENTIONS Patients were randomly assigned to receive celecoxib, 400 mg twice per day (2 and 4 times the maximum RA and OA dosages, respectively; n = 3987); ibuprofen, 800 mg 3 times per day (n = 1985); or diclofenac, 75 mg twice per day (n = 1996). Aspirin use for cardiovascular prophylaxis (≤325 mg/d) was permitted. MAIN OUTCOME MEASURES Incidence of prospectively defined symptomatic upper GI ulcers and ulcer complications (bleeding, perforation, and obstruction) and other adverse effects during the 6-month treatment period. RESULTS For all patients, the annualized incidence rates of upper GI ulcer complications alone and combined with symptomatic ulcers for celecoxib vs NSAIDs were 0.76% vs 1.45% (P = .09) and 2.08% vs 3.54% (P = .02), respectively. For patients not taking aspirin, the annualized incidence rates of upper GI ulcer complications alone and combined with symptomatic ulcers for celecoxib vs NSAIDs were 0.44% vs 1.27% (P = .04) and 1.40% vs 2.91% (P = .02). For patients taking aspirin, the annualized incidence rates of upper GI ulcer complications alone and combined with symptomatic ulcers for celecoxib vs NSAIDs were 2.01% vs 2.12% (P = .92) and 4.70% vs 6.00% (P = .49). Fewer celecoxib-treated patients than NSAID-treated patients experienced chronic GI blood loss, GI intolerance, hepatotoxicity, or renal toxicity. No difference was noted in the incidence of cardiovascular events between celecoxib and NSAIDs, irrespective of aspirin use. CONCLUSIONS In this study, celecoxib, at dosages greater than those indicated clinically, was associated with a lower incidence of symptomatic ulcers and ulcer complications combined, as well as other clinically important toxic effects, compared with NSAIDs at standard dosages. The decrease in upper GI toxicity was strongest among patients not taking aspirin concomitantly.