According to the trial results, RZV demonstrated a 79.7% vaccine efficacy (VE) in patients aged 50 years and older cumulatively within the 6- to 11-year period after vaccination (95% CI 73.7–84.6). Adults aged 70 years and older showed positive results as well, with a 73.1% VE observed cumulatively within the 6- to 11-year period after vaccination (95% CI 62.9–80.9), indicating that VE is high across both age groups. Further, at year 11, an 82% VE was observed in adults (95% CI 63.0–92.2), with VE remaining high each year following initial vaccination.1
“These final data demonstrate continued protection over more than a decade with high efficacy maintained in both the 50 plus and 70 plus age groups. Infectious diseases like shingles pose a significant risk to adults due to the natural decline in our immune system, and these data represent a remarkable advancement in our understanding of what can be achieved long-term for effective protection against shingles,” said Javier Díez-Domingo, PhD, principal investigator, Foundation for the Promotion of Health and Biomedical Research of the Valencian Community, Spain, in a press release.1
According to the investigators, there were no new safety concerns identified during the trial. Further, no serious adverse events (AEs) were considered to be related to the RZV vaccination. The most common AEs reported by the patients who received the RZV vaccine were pain at the injection site, myalgia, fatigue, and headache; however, most of these occurrences were mild to moderate in intensity and lasted less than 3 days. The study data will be presented at the European Society of Clinical Microbiology and Infectious Diseases Global in Barcelona, Spain, from April 27, 2024, to April 30, 2024.1
“These data go far beyond the typical long-term follow-up period for a trial, tracking the efficacy of vaccination for some participants as they aged into their 70s, 80s, and 90s,” said Phil Dormitzer, senior vice president, Head of Vaccines R&D, in the press release. "With the vaccine now included in many national immunization programs around the world, these data add to the body of evidence on the extended long-term protection against shingles and provide further confidence to inform public immunization strategies."1
References
2. A Long-term Follow-up Study (ZOE-LTFU) of Two Studies 110390 (ZOSTER-006) and 113077 (ZOSTER-022) to Assess the Efficacy, Safety, and Immunogenicity Persistence of GSK Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine and Assessment of 1 or 2 Additional Doses in Two Subgroups of Older Adults.ClinicalTrials.gov identifier: NCT02723773. Updated March 5, 2024. Accessed April 22, 2024. https://clinicaltrials.gov/study/NCT02723773