4.8 Article

Cardiovascular Safety of Lorcaserin in Overweigh or Obese Patients

期刊

NEW ENGLAND JOURNAL OF MEDICINE
卷 379, 期 12, 页码 1107-1117

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MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1808721

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资金

  1. Eisai
  2. Merck
  3. Amgen
  4. AstraZeneca
  5. Sanofi Aventis
  6. Arena
  7. Bristol-Myers Squibb
  8. Daiichi Sankyo
  9. Eli Lilly
  10. Janssen
  11. Aegerion
  12. Allergan
  13. Angelmed
  14. Boehringer Ingelheim
  15. Boston Clinical Research Institute
  16. Icon Clinical
  17. Lexicon
  18. St. Jude Medical
  19. Xoma
  20. Sanofi US
  21. Novo Nordisk
  22. Astra-Zeneca
  23. Merck Sharp
  24. Dohme
  25. Metavant
  26. Esperion
  27. Bristol-Myers Squibb/Pfizer
  28. Novartis
  29. GlaxoSmithKline
  30. Bayer
  31. Sanofi
  32. Omthera Pharmaceuticals
  33. DalCor Pharmaceuticals
  34. Sirtex
  35. Acetelion
  36. CVS Caremark
  37. Dyrnamix
  38. Alnylam
  39. Ionis
  40. MyoKardia
  41. Biogen Idec
  42. Covance
  43. Dr. Reddy's Laboratories
  44. Elsevier PracticeUpdate Cardiology
  45. Servier
  46. MD Conference Express
  47. Medscape
  48. Academic CME
  49. Paradigm

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BACKGROUND Lorcaserin, a selective serotonin 2C receptor agonist that modulates appetite, has proven efficacy for weight management in overweight or obese patients. The cardiovascular safety and efficacy of lorcaserin are undefined. METHODS We randomly assigned 12,000 overweight or obese patients with atherosclerotic cardiovascular disease or multiple cardiovascular risk factors to receive either lorcaserin (10 mg twice daily) or placebo. The primary safety outcome of major cardiovascular events (a composite of cardiovascular death, myocardial infarction, or stroke) was assessed at an interim analysis to exclude a noninferiority boundary of 1.4. If noninferiority was met, the primary cardiovascular efficacy outcome (a composite of major cardiovascular events, heart failure, hospitalization for unstable angina, or coronary revascularization (extended major cardiovascular events)) was assessed for superiority at the end of the trial. RESULTS At 1 year, weight loss of at least 5% had occurred in 1986 of 5135 patients (38.7%) in the lorcaserin group and in 883 of 5083 (17.4%) in the placebo group (odds ratio, 3.01; 95% confidence interval [CI], 2.74 to 3.30; P<0.001). Patients in the lorcaserin group had slightly better values with respect to cardiac risk factors (including blood pressure, heart rate, glycemic control, and lipids) than those in the placebo group. During a median follow-up of 3.3 years, the rate of the primary safety outcome was 2.0% per year in the lorcaserin group and 2.1% per year in the placebo group (hazard ratio, 0.99; 95% CI, 0.85 to 1.14; P<0.001 for noninferiority); the rate of extended major cardiovascular events was 4.1% per year and 4.2% per year, respectively (hazard ratio, 0.97; 95% CI, 0.87 to 1.07; P=0.55). Adverse events of special interest were uncommon, and the rates were generally similar in the two groups, except for a higher number of patients with serious hypoglycemia in the lorcaserin group (13 vs. 4, P=0.04). CONCLUSIONS In a high-risk population of overweight or obese patients, lorcaserin facilitated sustained weight loss without a higher rate of major cardiovascular events than that with placebo.

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