Cited by 947Cervical Cancer and HPV ResearchWomen's cancer prevention and managementGlobal Cancer Incidence and Screening

The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index; 17 of the 59 sources its claims cite were checked for support.

Impact of HPV vaccination and cervical screening on cervical cancer elimination: a comparative modelling analysis in 78 low-income and lower-middle-income countries

Open access

Abstract

BACKGROUND: The WHO Director-General has issued a call for action to eliminate cervical cancer as a public health problem. To help inform global efforts, we modelled potential human papillomavirus (HPV) vaccination and cervical screening scenarios in low-income and lower-middle-income countries (LMICs) to examine the feasibility and timing of elimination at different thresholds, and to estimate the number of cervical cancer cases averted on the path to elimination. METHODS: The WHO Cervical Cancer Elimination Modelling Consortium (CCEMC), which consists of three independent transmission-dynamic models identified by WHO according to predefined criteria, projected reductions in cervical cancer incidence over time in 78 LMICs for three standardised base-case scenarios: girls-only vaccination; girls-only vaccination and once-lifetime screening; and girls-only vaccination and twice-lifetime screening. Girls were vaccinated at age 9 years (with a catch-up to age 14 years), assuming 90% coverage and 100% lifetime protection against HPV types 16, 18, 31, 33, 45, 52, and 58. Cervical screening involved HPV testing once or twice per lifetime at ages 35 years and 45 years, with uptake increasing from 45% (2023) to 90% (2045 onwards). The elimination thresholds examined were an average age-standardised cervical cancer incidence of four or fewer cases per 100 000 women-years and ten or fewer cases per 100 000 women-years, and an 85% or greater reduction in incidence. Sensitivity analyses were done, varying vaccination and screening strategies and assumptions. We summarised results using the median (range) of model predictions. FINDINGS: Girls-only HPV vaccination was predicted to reduce the median age-standardised cervical cancer incidence in LMICs from 19·8 (range 19·4-19·8) to 2·1 (2·0-2·6) cases per 100 000 women-years over the next century (89·4% [86·2-90·1] reduction), and to avert 61·0 million (60·5-63·0) cases during this period. Adding twice-lifetime screening reduced the incidence to 0·7 (0·6-1·6) cases per 100 000 women-years (96·7% [91·3-96·7] reduction) and averted an extra 12·1 million (9·5-13·7) cases. Girls-only vaccination was predicted to result in elimination in 60% (58-65) of LMICs based on the threshold of four or fewer cases per 100 000 women-years, in 99% (89-100) of LMICs based on the threshold of ten or fewer cases per 100 000 women-years, and in 87% (37-99) of LMICs based on the 85% or greater reduction threshold. When adding twice-lifetime screening, 100% (71-100) of LMICs reached elimination for all three thresholds. In regions in which all countries can achieve cervical cancer elimination with girls-only vaccination, elimination could occur between 2059 and 2102, depending on the threshold and region. Introducing twice-lifetime screening accelerated elimination by 11-31 years. Long-term vaccine protection was required for elimination. INTERPRETATION: Predictions were consistent across our three models and suggest that high HPV vaccination coverage of girls can lead to cervical cancer elimination in most LMICs by the end of the century. Screening with high uptake will expedite reductions and will be necessary to eliminate cervical cancer in countries with the highest burden. FUNDING: WHO, UNDP, UN Population Fund, UNICEF-WHO-World Bank Special Program of Research, Development and Research Training in Human Reproduction, Canadian Institute of Health Research, Fonds de recherche du Québec-Santé, Compute Canada, National Health and Medical Research Council Australia Centre for Research Excellence in Cervical Cancer Control.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

In a comparative modelling analysis using three independent transmission-dynamic models, high-coverage girls-only HPV vaccination was projected to eliminate cervical cancer in most of 78 LMICs by the end of the century, with screening accelerating and extending elimination. Adding twice-lifetime screening was projected to achieve elimination in all 78 LMICs under all three thresholds and avert 74·1 million cases by 2120.

Key findings

  • Girls-only HPV vaccination reduced median age-standardised cervical cancer incidence in LMICs from 19·8 (range 19·4–19·8) to 2·1 (2·0–2·6) cases per 100 000 women-years over the next century (89·4% [86·2–90·1] reduction), averting 61·0 million (60·5–63·0) cases.
  • Adding twice-lifetime screening reduced incidence to 0·7 (0·6–1·6) cases per 100 000 women-years (96·7% [91·3–96·7] reduction) and averted an extra 12·1 million (9·5–13·7) cases; overall, intensive vaccination plus twice-lifetime screening was estimated to avert 74·1 million (70·4–75·1) cases by 2120.
  • Girls-only vaccination was predicted to eliminate cervical cancer in 60% (58–65) of LMICs at the ≤4 cases per 100 000 women-years threshold, 99% (89–100) at ≤10, and 87% (37–99) at ≥85% reduction; adding twice-lifetime screening reached 100% (71–100) for all three thresholds. Where vaccination alone sufficed, elimination occurred between 2059 and 2102, and screening accelerated elimination by 11–31 years.
  • Countries with the highest incidence (>25 cases per 100 000 women-years, mainly in sub-Saharan Africa) were not predicted to eliminate by vaccination alone; screening was required, and long-term vaccine protection was necessary for elimination.

Methods

  • WHO Cervical Cancer Elimination Modelling Consortium comparative modelling analysis using three independently developed transmission-dynamic models (HPV-ADVISE, Harvard, Policy1-Cervix) selected by predefined criteria, projecting cervical cancer incidence for 78 LMICs from 2020 to 2120.
  • Base-case scenarios: girls-only vaccination at age 9 years (catch-up to age 14 years), 90% coverage, 100% efficacy against HPV types 16, 18, 31, 33, 45, 52, and 58, lifelong protection; plus once-lifetime screening at age 35 years or twice-lifetime screening at ages 35 and 45 years, using HPV testing with uptake 45% (2023), 70% (2030), and 90% (2045 onwards), 100% treatment efficacy, and 10% loss to follow-up.
  • Outcomes were age-standardised cervical cancer incidence, relative reduction versus status quo, and cases averted; elimination thresholds were ≤4 and ≤10 cases per 100 000 women-years and ≥85% reduction; results reported as median (range) across models, with sensitivity analyses varying vaccination and screening assumptions.

Limitations

  • Stated: projections span >100 years, over which demographic, behavioural, and technological changes are anticipated; population growth affects cases averted (62 million with low UN population projections and 88 million with high projections versus 74 million base-case) but is expected to have minimal impact on age-standardised elimination timing, while changing sexual behaviour could lengthen time to elimination.
  • Stated: the analysis assumes intensive scale-up and 90% vaccination and screening uptake; slower scale-up would delay elimination and reduce cases averted but would not affect whether elimination can be achieved.
  • Stated: models omit plausible HIV–HPV biological interactions, potentially overestimating vaccination impact in high HIV prevalence settings (5 of 78 LMICs have HIV prevalence ≥10%), and rely on GLOBOCAN incidence estimates that may be underestimated, which could delay elimination. Evident: base-case assumptions of 100% vaccine efficacy, lifelong protection, 100% treatment efficacy, and only 10% loss to follow-up are idealized relative to real-world implementation, though sensitivity analyses partially address duration of protection and coverage.

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Integrity signals

Registry

Crossref · 10.1016/s0140-6736(20)30068-4

Cites

38 of 38 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

73 Own result · 30 Own interpretation · 9 No full text of the sources · 8 Partly supported · 6 Sources not found · 6 Own method · 6 No basis given · 3 Supported · 3 Supported so far · 1 Not supported · 1 Not checked yet · accuracy not yet measured

Show all 100 claims

  • It may state two separate claims as one. 31
  • Probably not a substantial claim. 16
46 of 46
  • The authors state this as an assumption.

    HPV vaccines are prophylactic and vaccination produces post-vaccination herd effects.

    “All models assume that HPV vaccines are prophylactic and capture post-vaccination herd effects.”
  • The authors state this as an assumption.

    Countries follow SAGE recommendations.

    “assuming countries follow SAGE recommendations”
  • The authors state this as an assumption.

    Supply constraints are relieved over the next decade.

    “provided supply constraints are relieved over the next decade”
  • The authors state this as an assumption.

    Intensive scale-up and 90% uptake of HPV vaccination and cervical screening.

    “we assumed intensive scale-up and 90% uptake of HPV vaccination and cervical screening.”
4 of 4

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Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

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2 of 2

Citations

Cites

Show all 37 references

Research works printed but not linked: 1

  1. 2019, Immunization and Vaccine-related Implementation Research Advisory Committee (IVIR-AC) recommendations. Sept 2018, Wkly Epidemiol Rec, 94, 5

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Metadata

Authors
Brisson, M., Kim, J. J., Canfell, K., Drolet, M., Gingras, G., Burger, E. A., Martin, D., Simms, K. T., Bénard, É., Boily, M.-C., Sy, S., Regan, C., Keane, A., Caruana, M., Nguyen, D. T. N., Smith, M. A., Laprise, J.-F., Jit, M., Alary, M., Bray, F., Fidarova, E., Elsheikh, F., Bloem, P. J. N., Broutet, N., & Hutubessy, R.
Affiliations
  • Université Laval (CA)
  • Harvard University (US)
  • The University of Sydney (AU)
  • Centre de recherche du CHU de Québec-Université Laval (CA)
  • Public Health England (GB)
  • Institut National de Santé Publique du Québec (CA)
  • Centre international de recherche sur le cancer (FR)
  • World Health Organization (CH)
Corresponding author
Brisson, Marc
Venue
The Lancet
Publisher
Elsevier BV
Published
2020-02
Volume
395
Issue
10224
Pages
575-590
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
OpenAlex
W3003249044
Cited by
943
References
37
Citations by year
2026: 131 · 2025: 174 · 2024: 177 · 2023: 147 · 2022: 126 · 2021: 137 · 2020: 50
FWCI
70.75
Type
journal article
Language
en
Open access
Locations
  • The Lancet (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
  • PubMed Central (submittedVersion, cc-by-nc-nd)
  • Spiral (Imperial College London) (submittedVersion, other-oa)
Funders
European Union (MR/R015600/1)
Topics
  • Health Sciences › Medicine › Epidemiology › Cervical Cancer and HPV Research
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Women's cancer prevention and management
  • Health Sciences › Medicine › Oncology › Global Cancer Incidence and Screening
Keywords
cervical cancer elimination, HPV vaccination, cervical cancer screening, cervical cancer incidence, vaccination coverage, screening uptake, incidence reduction, case averted
MeSH terms
Adult, Uterine Cervical Neoplasms, Developing Countries, Feasibility Studies, Female, Humans, Income, Mass Screening, Models, Biological, Vaccination, Incidence, Papillomavirus Infections, Papillomavirus Vaccines, Early Detection of Cancer

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