The comparative efficacy and safety of herpes zoster vaccines: A network meta-analysis

被引:28
|
作者
McGirr, Ashleigh [1 ]
Widenmaier, Robyn [1 ]
Curran, Desmond [2 ]
Espie, Emmanuelle [2 ]
Mrkvan, Tomas [2 ]
Oostvogels, Lidia [2 ,9 ]
Simone, Benedetto [3 ]
McElhaney, Janet E. [4 ]
Burnett, Heather [5 ]
Haeussler, Katrin [6 ]
Thano, Adriana [7 ]
Wang, Xuan [8 ]
Newson, Rachel S. [7 ]
机构
[1] GSK Canada, 7333 Mississauga Rd N, Mississauga, ON L5N 6L4, Canada
[2] GSK, 20 Ave Fleming, B-1300 Wavre, Belgium
[3] GSK, Stockley Pk West,1-3 Ironbridge Rd, Uxbridge UB11 1BT, Middx, England
[4] Hlth Sci North Res Inst, 41 Ramsey Lake Rd, Sudbury, ON P3E 5J1, Canada
[5] Evidera, 7575 Trans Canada Hwy,Suite 404, St Laurent, PQ H4T 1V6, Canada
[6] ICON Plc, Konrad Zuse Pl 11, D-81829 Munich, Germany
[7] ICON Plc, De Molen 84, NL-3995 AX Houten, Netherlands
[8] ICON Plc, Klarabergsviadukten 90 Hus D, S-11164 Stockholm, Sweden
[9] CureVac AG, Tubingen, Germany
关键词
Comparative efficacy; Herpes zoster; Post-herpetic neuralgia; Reactogenicity; Safety; Vaccine; ADULTS GREATER-THAN-OR-EQUAL-TO-60 YEARS; SHINGLES PREVENTION; SUBUNIT VACCINE; DOUBLE-BLIND; IMMUNOGENICITY; TOLERABILITY;
D O I
10.1016/j.vaccine.2019.04.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: We estimated the relative efficacy and safety of vaccines for prevention of herpes zoster (HZ) using network meta-analysis (NMA) based on evidence from randomized controlled trials. Methods: A systematic literature review evaluated two different HZ vaccines: adjuvanted recombinant zoster vaccine (RZV) and zoster vaccine live (ZVL), with different formulations assessed. Detailed feasibility assessment indicated that a NMA was feasible for efficacy (incidence of HZ and postherpetic neuralgia [PHN]) and safety (serious adverse events [SAE] and reactogenicity [injection-site reactions, systemic reaction]) outcomes. Primary analyses included frequentist NMAs with fixed effects for efficacy outcomes, due to limited data availability, and both fixed and random effects for safety and reactogenicity outcomes. As age is a known effect modifier of vaccine efficacy (VE), VE analyses were stratified by age. Results: RZV demonstrated significantly higher HZ efficacy than ZVL in adults >= 60 years of age (YOA) (VERZV = 0.92 (95% confidence interval [95%Cl]: 0.88, 0.94), VEZVL = 0.51 (95%Cl: 0.44, 0.57)) and adults >= 70 YOA (VERZV = 0.91 (95%Cl: 0.87, 0.94), VEZVL = 0.37 (95%Cl: 0.25, 0.48)). Similarly, RZV demonstrated significantly higher PHN efficacy than ZVL in adults >= 60 YOA (VERZV = 0.89 (95%Cl: 0.70, 0.96), VEZVL = 0.66 (95%Cl: 0.48, 0.78)) and adults >= 70 YOA (VERZV = 0.89 (95%Cl: 0.69, 0.96), VEZVL = 0.67 (95%Cl: 0.44, 0.80)). RZV was associated with significantly more injection-site and systemic reactions compared to most formulations of ZVL and placebo, however definitions and data collection procedures differed across the included studies. There were no statistically significant differences found between RZV and any formulation of ZVL or placebo for SAES. Conclusion: RZV is significantly more effective in reducing HZ and PHN incidence in adults >= 60 YOA, compared with ZVL. As anticipated with an adjuvanted vaccine, RZV results in more reactogenicity following immunization. No differences in SAES were found between RZV and ZVL. (C) 2019 GlaxoSmithKline SA. Published by Elsevier Ltd.
引用
收藏
页码:2896 / 2909
页数:14
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