4.8 Article

Combined Analysis of Asthma Safety Trials of Long-Acting beta(2)-Agonists

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 378, Issue 26, Pages 2497-2505

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1716868

Keywords

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Funding

  1. 3M
  2. Boehringer Ingelheim
  3. AstraZeneca
  4. GlaxoSmithKline
  5. Novartis
  6. Sanofi-Regeneron
  7. Teva
  8. Boston Scientific
  9. Genentech
  10. Cipla
  11. ALK
  12. Vectura Group
  13. Merck
  14. Takeda
  15. Hoffmann-La Roche
  16. Actelion
  17. Chiesi
  18. Sanofi-Aventis
  19. Cephalon
  20. Menarini
  21. Sanofi Regeneron
  22. Medimmune
  23. Teva Pharmaceutical Industries
  24. Intermune
  25. Sanofi
  26. Berlin-Chemie
  27. ICON Clinical Research
  28. Astra-Zeneca

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BACKGROUND Safety concerns regarding long-acting beta(2)-agonists (LABAs) in asthma management were initially identified in a large postmarketing trial in which the risk of death was increased. In 2010, the Food and Drug Administration (FDA) mandated that the four companies marketing LABAs for asthma perform prospective, randomized, controlled trials comparing the safety of combination therapy with a LABA plus an inhaled glucocorticoid with that of an inhaled glucocorticoid alone in adolescents (12 to 17 years of age) and adults. In conjunction with the FDA, the manufacturers harmonized their trial methods to allow an independent joint oversight committee to provide a final combined analysis of the four trials. METHODS As members of the joint oversight committee, we performed a combined analysis of the four trials comparing an inhaled glucocorticoid plus a LABA (combination therapy) with an inhaled glucocorticoid alone. The primary outcome was a composite of asthma-related intubation or death. Post hoc secondary outcomes included serious asthma-related events and asthma exacerbations. RESULTS Among the 36,010 patients in the intention-to-treat study, there were three asthma-related intubations (two in the inhaled-glucocorticoid group and one in the combination- therapy group) and two asthma-related deaths (both in the combinationtherapy group) in 4 patients. In the secondary analysis of serious asthma-related events (a composite of hospitalization, intubation, or death), 108 of 18,006 patients (0.60%) in the inhaled-glucocorticoid group and 119 of 18,004 patients (0.66%) in the combination-therapy group had at least one composite event (relative risk in the combination-therapy group, 1.09; 95% confidence interval [CI], 0.83 to 1.43; P = 0.55); 2100 patients in the inhaled-glucocorticoid group (11.7%) and 1768 in the combination-therapy group (9.8%) had at least one asthma exacerbation (relative risk, 0.83; 95% CI, 0.78 to 0.89; P<0.001). CONCLUSIONS Combination therapy with a LABA plus an inhaled glucocorticoid did not result in a significantly higher risk of serious asthma-related events than treatment with an inhaled glucocorticoid alone but resulted in significantly fewer asthma exacerbations.

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