Table 3.
Cardiovascular endpoints in studies of selective COX2 inhibitors
| Drug (reference) | Study | Aspirin allowed | CV endpoints | Hazard ratios or incidence of CV endpoints | ||
|---|---|---|---|---|---|---|
| All | No aspirin | On aspirin | ||||
| Rofecoxib (Bombardier 2000) | VIGOR | No | MI | 4.25 (1.39−17.37) | Idem | Excluded |
| CV death | c0.2% vs 0.2%, NS | Idem | Excluded | |||
| Celecoxib (Silverstein 2000) | CLASS | Yes | MI, stroke or angina | 0.9% vs 1.0%, NS | 0.5% vs 0.4%, NS | nr |
| Etoricoxib (Cannon 2006; Laine 2007) | MEDAL | Stimulated | aAny thrombotic events | 0.95 (0.81−1.11) | d1.0% vs 1.0%, NS | d1.67% vs 1.87%, NS |
| aArterial thrombotic events | 0.96 (0.81−1.13) | nr | nr | |||
| a,bAPTC (all MI, stroke or vascular death) | 0.96 (0.79−1.16) | nr | nr | |||
| Lumiracoxib (Schnitzer 2004; Farkouh 2004) | TARGET | Yes | bAPTC (all MI, stroke or vascular death) | |||
| vs ibuprofen + naproxen | 1.14 (0.78–1.66) | 1.22 (0.74–2.02) | 1.04 (0.59–1.84) | |||
| vs ibuprofen | 0.76 (0.41–1.40) | 0.94 (0.44–2.04) | 0.56 (0.20–1.54) | |||
| vs naproxen | 1.46 (0.89–2.37) | 1.49 (0.76–2.92) | 1.42 (0.70–2.90) | |||
| Confirmed or probable MI (clinical and silent) | ||||||
| vs ibuprofen + naproxen | 1.31 (0.70–2.45) | 1.47 (0.63–3.39) | 1.14 (0.44–2.95) | |||
| vs ibuprofen | 0.66 (0.21–2.09) | 0.75 (0.20–2.79) | 0.47 (0.04–5.14) | |||
| vs naproxen | 1.77 (0.82–3.84) | 2.37 (0.74–7.55) | 1.36 (0.47–3.93) | |||
Per-protocol analysis, similar results after ITT analysis.
APTC, Anti-Platelet Trialists' Collaboration endpoint.
incidence.
events per 100 patient yrs.
Abbreviations: nr, not reported.