Evidence map›Paper›PMID 35241461›Full record

ArticleBMJ global health2022

Towards the elimination of cervical cancer in low-income and lower-middle-income countries: modelled evaluation of the effectiveness and cost-effectiveness of point-of-care HPV self-collected screening and treatment in Papua New Guinea.

Diep Thi Ngoc Nguyen, Kate T Simms, Adam Keane, Glen Mola, John Walpe Bolnga, Joseph Kuk, Pamela J Toliman, Steven G Badman, Marion Saville, John Kaldor and 2 more

Abstract read
In one paragraph

Article in BMJ global health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Diep Thi Ngoc NguyenDaffodil Centre, The University of Sydney, Sydney, New South Wales, Australia diep.nguyen@nswcc.org.au.ORCID 0000-0002-7103-7877
Kate T SimmsDaffodil Centre, The University of Sydney, Sydney, New South Wales, Australia.
Adam KeaneDaffodil Centre, The University of Sydney, Sydney, New South Wales, Australia.
Glen MolaDepartment of Reproductive Health, Obstetrics and Gynecology, School of Medicine and Health Sciences, University of Papua New Guinea, Port Moresby, CND, Papua New Guinea.
John Walpe BolngaDepartment of Obstetrics and Gynecology, Modilion Hospital, Mango, Madang, Papua New Guinea.ORCID 0000-0003-1214-9817
Joseph KukDepartment of Obstetrics and Gynecology, Mt Hagen Provincial Hospital, Mt Hagen, Western Highlands Province, Papua New Guinea.
Pamela J TolimanKirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
Steven G BadmanKirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
Marion SavilleAustralian Centre for the Prevention of Cervical Cancer, Melbourne, Victoria, Australia.
John KaldorKirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
Andrew VallelyKirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
Karen CanfellDaffodil Centre, The University of Sydney, Sydney, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWHO has launched updated cervical screening guidelines, including provisions for primary HPV screen-and-treat. Papua New Guinea (PNG) has a high burden of cervical cancer, but no national cervical screening programme. We recently completed the first field trials of a screen-and-treat algorithm using point-of-care self-collected HPV and same-day treatment (hereafter self-collected HPV S&T) and showed this had superior clinical performance and acceptability to visual inspection of the cervix with acetic acid (VIA). We, therefore, evaluated the effectiveness, cost-effectiveness and resource implications of a national cervical screening programme using self-collected HPV S&T compared with VIA in PNG.

methodsAn extensively validated platform ('Policy1-Cervix') was calibrated to PNG. A total of 38 strategies were selected for investigation, and these incorporated variations in age ranges and screening frequencies and allowed for the identification of the optimal strategy across a wide range of possibilities. A selection of strategies that were identified as being the most effective and cost-effective were then selected for further investigation for longer-term outcomes and budget impact estimation. In the base case, we assumed primary HPV testing has a sensitivity to cervical intraepithelial neoplasia 2 (CIN2+) + of 91.8% and primary VIA of 51.5% based on our earlier field evaluation combined with evidence from the literature. We conservatively assumed HPV sampling and testing would cost US$18. Costs were estimated from a service provider perspective based on data from local field trials and local consultation.

resultsSelf-collected HPV S&T was more effective and more cost-effective than VIA. Either twice or thrice lifetime self-collected HPV S&T would be cost-effective at 0.5× gross domestic product (GDP) per capita (incremental cost-effectiveness ratio: US$460-US$656/life-years saved; 1GDPper-capita: US$2829 or PGK9446 (year 2019)) and could prevent 33 000-42 000 cases and 23 000-29 000 deaths in PNG over the next 50 years, if scale-up reached 70% coverage from 2023.

conclusionSelf-collected HPV S&T was effective and cost-effective in the high-burden, low-resource setting of PNG, and, if scaled-up rapidly, could prevent over 20 000 deaths over the next 50 years. VIA screening was not effective or cost-effective. These findings support, at a country level, WHO updated cervical screening guidelines and indicate that similar approaches could be appropriate for other low-resource settings.

Indexed as

Papillomavirus InfectionsUterine Cervical NeoplasmsCost-Benefit AnalysisDeveloping CountriesEarly Detection of CancerFemaleHumansPapua New GuineaPoint-of-Care Systemscancerhealth economicsmathematical modellingscreening

Identifiers

PMID35241461
PMCPMC8896000

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.