Cost-effectiveness of 20-valent versus 15-valent pneumococcal conjugate vaccines for infants in the Netherlands, taking into account indirect effects and adult vaccination

The 20-valent pneumococcal conjugate vaccine (PCV20) is approved for EU infants in a 3 + 1 schedule. In the Netherlands, PCV15 (2 + 1) was recently introduced into the national immunization program for infants, while a PCV20 program for older adults is being implemented. We evaluated the cost-effectiveness of replacing PCV15 (2 + 1) with PCV20 (3 + 1) for Dutch infants, taking into account indirect effects and their impact on the adult PCV20 program. A static, population-based Markov model estimated societal costs and quality-adjusted life-year (QALY) losses due to invasive pneumococcal disease and hospitalized non-invasive pneumococcal pneumonia in the Netherlands over a 10-year time horizon. Disease rates were based on a mature PCV10 infant program, with projections made for implementing PCV15 or PCV20, extrapolating magnitudes of indirect protection and serotype replacement from prior PCV13 programs. Among adults ≥ 60 years, PCV20 uptake was 55–70%, depending on age, with a scenario analysis exploring PCV21. Dutch vaccine list prices were applied. Replacing PCV15 (2 + 1) with PCV20 (3 + 1) in infants yielded QALY gains for children and adults aged < 60 years. However, among adults aged ≥ 60 years, early QALY gains were offset by later losses as indirect effects shifted disease to non-PCV20 serotypes, reducing the benefits of the adult PCV20 program. Over 10 years, this resulted in a net population-level loss of 3476 QALYs and €192 million in additional costs, making PCV15 (2 + 1) the dominant strategy. No net QALY loss was found when comparing PCV20 (3 + 1) with PCV15 (3 + 1) alongside an adult PCV21 program, as PCV21 includes eleven non-PCV20 serotypes. However, the incremental cost-effectiveness ratio was €304,781/QALY gained, well above conventional Dutch thresholds of €20,000–€50,000/QALY gained. Results were sensitive to magnitudes of indirect effects, time horizon, and vaccination costs of PCV20 versus PCV15. Replacing PCV15 (2 + 1) with PCV20 (3 + 1) for Dutch infants likely results in a net population-level health loss over 10 years when paired with a PCV20 program for older adults. If compared alongside an adult PCV21 program, no net health loss was found, but PCV20 (3 + 1) was not cost-effective at current list prices. Considering adult vaccination programs is essential when evaluating infant PCV strategies.

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Journal
BMC Medicine
Published
2026-11-06
DOI
https://doi.org/10.1186/s12916-026-05378-7
Primary Topic
Pneumonia and Respiratory Infections
Type
article
Field-Weighted Citation Impact
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article

Cost-effectiveness of 20-valent versus 15-valent pneumococcal conjugate vaccines for infants in the Netherlands, taking into account indirect effects and adult vaccination

Jacco Wallinga, Hester E. de Melker, Pieter T. de Boer, Elisabeth A. M. Sanders et al.
4 links
BMC Medicine
Pneumonia and Respiratory Infections
article

Cost-effectiveness of 20-valent versus 15-valent pneumococcal conjugate vaccines for infants in the Netherlands, taking into account indirect effects and adult vaccination

Jacco Wallinga, Hester E. de Melker, Pieter T. de Boer, Elisabeth A. M. Sanders, Anneke Steens, Albert Jan van Hoek, Mirjam J. Knol
article en

Abstract

The 20-valent pneumococcal conjugate vaccine (PCV20) is approved for EU infants in a 3 + 1 schedule. In the Netherlands, PCV15 (2 + 1) was recently introduced into the national immunization program for infants, while a PCV20 program for older adults is being implemented. We evaluated the cost-effectiveness of replacing PCV15 (2 + 1) with PCV20 (3 + 1) for Dutch infants, taking into account indirect effects and their impact on the adult PCV20 program. A static, population-based Markov model estimated societal costs and quality-adjusted life-year (QALY) losses due to invasive pneumococcal disease and hospitalized non-invasive pneumococcal pneumonia in the Netherlands over a 10-year time horizon. Disease rates were based on a mature PCV10 infant program, with projections made for implementing PCV15 or PCV20, extrapolating magnitudes of indirect protection and serotype replacement from prior PCV13 programs. Among adults ≥ 60 years, PCV20 uptake was 55–70%, depending on age, with a scenario analysis exploring PCV21. Dutch vaccine list prices were applied. Replacing PCV15 (2 + 1) with PCV20 (3 + 1) in infants yielded QALY gains for children and adults aged < 60 years. However, among adults aged ≥ 60 years, early QALY gains were offset by later losses as indirect effects shifted disease to non-PCV20 serotypes, reducing the benefits of the adult PCV20 program. Over 10 years, this resulted in a net population-level loss of 3476 QALYs and €192 million in additional costs, making PCV15 (2 + 1) the dominant strategy. No net QALY loss was found when comparing PCV20 (3 + 1) with PCV15 (3 + 1) alongside an adult PCV21 program, as PCV21 includes eleven non-PCV20 serotypes. However, the incremental cost-effectiveness ratio was €304,781/QALY gained, well above conventional Dutch thresholds of €20,000–€50,000/QALY gained. Results were sensitive to magnitudes of indirect effects, time horizon, and vaccination costs of PCV20 versus PCV15. Replacing PCV15 (2 + 1) with PCV20 (3 + 1) for Dutch infants likely results in a net population-level health loss over 10 years when paired with a PCV20 program for older adults. If compared alongside an adult PCV21 program, no net health loss was found, but PCV20 (3 + 1) was not cost-effective at current list prices. Considering adult vaccination programs is essential when evaluating infant PCV strategies.

BMC Medicine
Leiden University Medical Center (NL), University Medical Center Utrecht (NL), National Institute for Public Health and the Environment (NL)
Ministerie van Volksgezondheid, Welzijn en Sport
Good health and well-being
Openalex Percentile: Top 14%
Pneumonia and Respiratory Infections
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