Polysaccharide Conjugate Vaccine against Pneumococcal Pneumonia in Adults

Marc J. M. Bonten(University Medical Center Utrecht), Susanne M. Huijts(University Medical Center Utrecht), Marieke Bolkenbaas(University Medical Center Utrecht), Chris Webber(Pfizer (United Kingdom)), Scott D. Patterson(Pfizer (United States)), Samantha Gault(Pfizer (United Kingdom)), Cornelis H. van Werkhoven(University Medical Center Utrecht), Anna M.M. van Deursen(University Medical Center Utrecht), Elisabeth A. M. Sanders(Wilhelmina Children's Hospital), Theo Verheij(University Medical Center Utrecht), Michael A. Patton(Pfizer (United Kingdom)), Anne McDonough(Pfizer (United Kingdom)), Anita Moradoghli-Haftvani(Pfizer (United Kingdom)), Helen Smith(Pfizer (United Kingdom)), Tracey Mellelieu(Pfizer (United Kingdom)), Michael W. Pride(Pfizer (United States)), Graham Crowther(Pfizer (United Kingdom)), Beate Schmöele-Thoma(Pfizer (Germany)), Daniel A. Scott(Pfizer (United States)), Kathrin U. Jansen(Pfizer (United States)), Rita Lobatto, Bas J. Oosterman, Nils L. Visser, Esther Caspers, Andre Smorenburg, Emilio A. Emini(Pfizer (United States)), William C. Gruber(Pfizer (United States)), Diederick E. Grobbee
New England Journal of Medicine
March 18, 2015
Cited by 1,233Open Access
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Abstract

BACKGROUND: Pneumococcal polysaccharide conjugate vaccines prevent pneumococcal disease in infants, but their efficacy against pneumococcal community-acquired pneumonia in adults 65 years of age or older is unknown. METHODS: In a randomized, double-blind, placebo-controlled trial involving 84,496 adults 65 years of age or older, we evaluated the efficacy of 13-valent polysaccharide conjugate vaccine (PCV13) in preventing first episodes of vaccine-type strains of pneumococcal community-acquired pneumonia, nonbacteremic and noninvasive pneumococcal community-acquired pneumonia, and invasive pneumococcal disease. Standard laboratory methods and a serotype-specific urinary antigen detection assay were used to identify community-acquired pneumonia and invasive pneumococcal disease. RESULTS: In the per-protocol analysis of first episodes of infections due to vaccine-type strains, community-acquired pneumonia occurred in 49 persons in the PCV13 group and 90 persons in the placebo group (vaccine efficacy, 45.6%; 95.2% confidence interval [CI], 21.8 to 62.5), nonbacteremic and noninvasive community-acquired pneumonia occurred in 33 persons in the PCV13 group and 60 persons in the placebo group (vaccine efficacy, 45.0%; 95.2% CI, 14.2 to 65.3), and invasive pneumococcal disease occurred in 7 persons in the PCV13 group and 28 persons in the placebo group (vaccine efficacy, 75.0%; 95% CI, 41.4 to 90.8). Efficacy persisted throughout the trial (mean follow-up, 3.97 years). In the modified intention-to-treat analysis, similar efficacy was observed (vaccine efficacy, 37.7%, 41.1%, and 75.8%, respectively), and community-acquired pneumonia occurred in 747 persons in the PCV13 group and 787 persons in placebo group (vaccine efficacy, 5.1%; 95% CI, -5.1 to 14.2). Numbers of serious adverse events and deaths were similar in the two groups, but there were more local reactions in the PCV13 group. CONCLUSIONS: Among older adults, PCV13 was effective in preventing vaccine-type pneumococcal, bacteremic, and nonbacteremic community-acquired pneumonia and vaccine-type invasive pneumococcal disease but not in preventing community-acquired pneumonia from any cause. (Funded by Pfizer; CAPITA ClinicalTrials.gov number NCT00744263.).


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