Global impact and cost-effectiveness of one-dose versus two-dose human papillomavirus vaccination schedules: a comparative modelling analysis.


Journal

BMC medicine
ISSN: 1741-7015
Titre abrégé: BMC Med
Pays: England
ID NLM: 101190723

Informations de publication

Date de publication:
28 08 2023
Historique:
received: 30 08 2022
accepted: 20 07 2023
medline: 29 8 2023
pubmed: 28 8 2023
entrez: 27 8 2023
Statut: epublish

Résumé

To eliminate cervical cancer as a public health problem, the World Health Organization had recommended routine vaccination of adolescent girls with two doses of the human papillomavirus (HPV) vaccine before sexual initiation. However, many countries have yet to implement HPV vaccination because of financial or logistical barriers to delivering two doses outside the infant immunisation programme. Using three independent HPV transmission models, we estimated the long-term health benefits and cost-effectiveness of one-dose versus two-dose HPV vaccination, in 188 countries, under scenarios in which one dose of the vaccine gives either a shorter duration of full protection (20 or 30 years) or lifelong protection but lower vaccine efficacy (e.g. 80%) compared to two doses. We simulated routine vaccination with the 9-valent HPV vaccine in 10-year-old girls at 80% coverage for the years 2021-2120, with a 1-year catch-up campaign up to age 14 at 80% coverage in the first year of the programme. Over the years 2021-2120, one-dose vaccination at 80% coverage was projected to avert 115.2 million (range of medians: 85.1-130.4) and 146.8 million (114.1-161.6) cervical cancers assuming one dose of the vaccine confers 20 and 30 years of protection, respectively. Should one dose of the vaccine provide lifelong protection at 80% vaccine efficacy, 147.8 million (140.6-169.7) cervical cancer cases could be prevented. If protection wanes after 20 years, 65 to 889 additional girls would need to be vaccinated with the second dose to prevent one cervical cancer, depending on the epidemiological profiles of the country. Across all income groups, the threshold cost for the second dose was low: from 1.59 (0.14-3.82) USD in low-income countries to 44.83 (3.75-85.64) USD in high-income countries, assuming one dose confers 30-year protection. Results were consistent across the three independent models and suggest that one-dose vaccination has similar health benefits to a two-dose programme while simplifying vaccine delivery, reducing costs, and alleviating vaccine supply constraints. The second dose may become cost-effective if there is a shorter duration of protection from one dose, cheaper vaccine and vaccination delivery strategies, and high burden of cervical cancer.

Sections du résumé

BACKGROUND
To eliminate cervical cancer as a public health problem, the World Health Organization had recommended routine vaccination of adolescent girls with two doses of the human papillomavirus (HPV) vaccine before sexual initiation. However, many countries have yet to implement HPV vaccination because of financial or logistical barriers to delivering two doses outside the infant immunisation programme.
METHODS
Using three independent HPV transmission models, we estimated the long-term health benefits and cost-effectiveness of one-dose versus two-dose HPV vaccination, in 188 countries, under scenarios in which one dose of the vaccine gives either a shorter duration of full protection (20 or 30 years) or lifelong protection but lower vaccine efficacy (e.g. 80%) compared to two doses. We simulated routine vaccination with the 9-valent HPV vaccine in 10-year-old girls at 80% coverage for the years 2021-2120, with a 1-year catch-up campaign up to age 14 at 80% coverage in the first year of the programme.
RESULTS
Over the years 2021-2120, one-dose vaccination at 80% coverage was projected to avert 115.2 million (range of medians: 85.1-130.4) and 146.8 million (114.1-161.6) cervical cancers assuming one dose of the vaccine confers 20 and 30 years of protection, respectively. Should one dose of the vaccine provide lifelong protection at 80% vaccine efficacy, 147.8 million (140.6-169.7) cervical cancer cases could be prevented. If protection wanes after 20 years, 65 to 889 additional girls would need to be vaccinated with the second dose to prevent one cervical cancer, depending on the epidemiological profiles of the country. Across all income groups, the threshold cost for the second dose was low: from 1.59 (0.14-3.82) USD in low-income countries to 44.83 (3.75-85.64) USD in high-income countries, assuming one dose confers 30-year protection.
CONCLUSIONS
Results were consistent across the three independent models and suggest that one-dose vaccination has similar health benefits to a two-dose programme while simplifying vaccine delivery, reducing costs, and alleviating vaccine supply constraints. The second dose may become cost-effective if there is a shorter duration of protection from one dose, cheaper vaccine and vaccination delivery strategies, and high burden of cervical cancer.

Identifiants

pubmed: 37635227
doi: 10.1186/s12916-023-02988-3
pii: 10.1186/s12916-023-02988-3
pmc: PMC10463590
doi:

Substances chimiques

Papillomavirus Vaccines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

313

Subventions

Organisme : CIHR
ID : FDN-143283
Pays : Canada

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Kiesha Prem (K)

Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK. kiesha.prem@lshtm.ac.uk.
Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore. kiesha.prem@lshtm.ac.uk.

Yoon Hong Choi (YH)

Modelling and Economics Unit, Data, Analytics and Surveillance, UK Health Security Agency, London, UK.

Élodie Bénard (É)

Centre de recherche du CHU de Québec - Université Laval, Québec, QC, Canada.

Emily A Burger (EA)

Center for Health Decision Science, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Department of Health Management and Health Economics, University of Oslo, Oslo, Norway.

Liza Hadley (L)

Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.
Disease Dynamics Unit, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.

Jean-François Laprise (JF)

Centre de recherche du CHU de Québec - Université Laval, Québec, QC, Canada.

Mary Caroline Regan (MC)

Center for Health Decision Science, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Mélanie Drolet (M)

Centre de recherche du CHU de Québec - Université Laval, Québec, QC, Canada.

Stephen Sy (S)

Center for Health Decision Science, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Kaja Abbas (K)

Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.

Allison Portnoy (A)

Center for Health Decision Science, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Jane J Kim (JJ)

Center for Health Decision Science, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Marc Brisson (M)

Centre de recherche du CHU de Québec - Université Laval, Québec, QC, Canada.
Department of Social and Preventive Medicine, Université Laval, Québec, QC, Canada.
MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London, UK.

Mark Jit (M)

Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK. mark.jit@lshtm.ac.uk.

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