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Original Research

Cost-effectiveness of nonavalent HPV vaccination in the Netherlands

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Pages 312-323 | Received 26 Dec 2023, Accepted 20 Feb 2024, Published online: 01 Mar 2024

Figures & data

Figure 1. Flow diagram of the model for cancers associated with human papillomavirus infection.

HPV, human papillomavirus.
Figure 1. Flow diagram of the model for cancers associated with human papillomavirus infection.

Figure 2. Forecasted incidence of nonavalent human papillomavirus vaccine-strain-attributable (a) cervical cancer and (b) all other anogenital plus head & neck cancers in the Netherlands with strategies using a bivalent or nonavalent human papillomavirus vaccine for individuals ≥9 years of age before sexual debut, with or without catch-up vaccination programs for individuals ≤26 years of age.

2vHPV, bivalent human papillomavirus vaccine; 9vHPV, nonavalent human papillomavirus vaccine.
The 2vHPV (status quo) strategy includes an immediate transition to vaccination of individuals ≥9 years of age (change from ≥12 years of age), with a year of catch-up vaccination for individuals 11 years of age in the year of transition. Vaccination coverage is assumed to continue at 70% for girls and 50% for boys. The 2vHPV plus catch-up strategy adds vaccination of individuals ≤26 years of age for 3 years such that coverage among this age group increases to 70% for girls/women and 50% for boys/men. The 9vHPV and 9vHPV plus catch-up strategies are as for the 2vHPV versions, but with an immediate switch from a bivalent to a nonavalent HPV vaccine.
Figure 2. Forecasted incidence of nonavalent human papillomavirus vaccine-strain-attributable (a) cervical cancer and (b) all other anogenital plus head & neck cancers in the Netherlands with strategies using a bivalent or nonavalent human papillomavirus vaccine for individuals ≥9 years of age before sexual debut, with or without catch-up vaccination programs for individuals ≤26 years of age.

Figure 3. Forecasted incidence of nonavalent human papillomavirus vaccine-strain-attributable anogenital warts in the Netherlands with strategies using a bivalent or nonavalent human papillomavirus vaccine for individuals ≥9 years of age before sexual debut, with or without catch-up vaccination programs for individuals ≤26 years of age.

2vHPV, bivalent human papillomavirus vaccine; 9vHPV, nonavalent human papillomavirus vaccine.
The 2vHPV (status quo) strategy includes an immediate transition to vaccination of individuals ≥9 years of age (change from ≥12 years of age), with a year of catch-up vaccination for individuals 11 years of age in the year of transition. Vaccination coverage is assumed to continue at 70% for girls and 50% for boys. The 9vHPV strategy is as for the 2vHPV versions, but with an immediate switch from a bivalent to a nonavalent HPV vaccine. The 9vHPV plus catch-up strategy adds vaccination of individuals ≤26 years of age for 3 years such that coverage among this age group increases to 70% for girls/women and 50% for boys/men. The data for the 2vHPV and 2vHPV plus catch-up strategies were identical, and therefore only the former is included in the graph.
Figure 3. Forecasted incidence of nonavalent human papillomavirus vaccine-strain-attributable anogenital warts in the Netherlands with strategies using a bivalent or nonavalent human papillomavirus vaccine for individuals ≥9 years of age before sexual debut, with or without catch-up vaccination programs for individuals ≤26 years of age.

Figure 4. Forecasted incidence of nonavalent human papillomavirus vaccine-strain-attributable (a) juvenile-onset and (b) adult-onset recurrent respiratory papillomatosis in the Netherlands with strategies using a bivalent or nonavalent human papillomavirus vaccine for individuals ≥9 years of age before sexual debut, with or without catch-up vaccination programs for individuals.

2vHPV, bivalent human papillomavirus vaccine; 9vHPV, nonavalent human papillomavirus vaccine.
The 2vHPV (status quo) strategy includes an immediate transition to vaccination of individuals ≥9 years of age (change from ≥12 years of age), with a year of catch-up vaccination for individuals 11 years of age in the year of transition. Vaccination coverage is assumed to continue at 70% for girls and 50% for boys. The 9vHPV strategy is as for the 2vHPV versions, but with an immediate switch from a bivalent to a nonavalent HPV vaccine. The 9vHPV plus catch-up strategy adds vaccination of individuals ≤26 years of age for 3 years such that coverage among this age group increases to 70% for girls/women and 50% for boys/men. The data for the 2vHPV and 2vHPV plus catch-up strategies were identical, and therefore only the former is included in the graphs.
Figure 4. Forecasted incidence of nonavalent human papillomavirus vaccine-strain-attributable (a) juvenile-onset and (b) adult-onset recurrent respiratory papillomatosis in the Netherlands with strategies using a bivalent or nonavalent human papillomavirus vaccine for individuals ≥9 years of age before sexual debut, with or without catch-up vaccination programs for individuals.

Table 1. Nonavalent human papillomavirus vaccine-strain-attributable disease cases and deaths in the Netherlands over 100 years with use of 9vHPV versus 2vHPV, with and without catch-up vaccination.

Table 2. Cost-effectiveness outcomes of four base-case human papillomavirus vaccination strategies in the Netherlands over 100 years.

Figure 5. Deterministic sensitivity analysis of the incremental cost-effectiveness ratios of 9vHPV versus 2vHPV human papillomavirus vaccination strategies for the Netherlands over 100 years.

2vHPV, bivalent human papillomavirus vaccine; 9vHPV, nonavalent human papillomavirus vaccine; ICER, incremental cost-effectiveness ratio; QALY, quality-adjusted life year. The 2vHPV (status quo) strategy includes an immediate transition to vaccination of individuals ≥9 years of age (change from ≥12 years of age), with a year of catch-up vaccination for individuals 11 years of age in the year of transition. Vaccination coverage is assumed to continue at 70% for girls and 50% for boys. The 9vHPV strategy is as for the 2vHPV versions, but with an immediate switch from a bivalent to a nonavalent HPV vaccine.
Figure 5. Deterministic sensitivity analysis of the incremental cost-effectiveness ratios of 9vHPV versus 2vHPV human papillomavirus vaccination strategies for the Netherlands over 100 years.

Table 3. Cost-effectiveness outcomes of four human papillomavirus vaccination strategies in the Netherlands over 100 years in scenarios of increased vaccination coverage or cross-protection against additional viral strains.

Supplemental material

Supplemental Material

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