Evidence map›Paper›PMID 39441790›Full record

ArticlePloS one2024

High-risk human papillomavirus testing for cervical cancer screening in Uganda: Considering potential harms and benefits in a low-resource setting.

Marat Sultanov, Jaap A R Koot, Geertruida H de Bock, Marcel J W Greuter, Jogchum J Beltman, Marlieke de Fouw, Janine de Zeeuw, Johnblack Kabukye, Jelle Stekelenburg, Jurjen van der Schans

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Marat SultanovGlobal Health Unit, Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.ORCID 0000-0002-5746-811X
Jaap A R KootGlobal Health Unit, Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.ORCID 0000-0002-6933-0302
Geertruida H de BockDepartment of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.ORCID 0000-0003-3104-4471
Marcel J W GreuterDepartment of Radiology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Jogchum J BeltmanDepartment of Gynecology, Leiden University Medical Center, Leiden University, Leiden, Netherlands.
Marlieke de FouwDepartment of Gynecology, Leiden University Medical Center, Leiden University, Leiden, Netherlands.ORCID 0000-0002-4488-4886
Janine de ZeeuwGlobal Health Unit, Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Johnblack KabukyeUganda Cancer Institute, Kampala, Uganda.ORCID 0000-0002-7864-1858
Jelle StekelenburgGlobal Health Unit, Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.ORCID 0000-0002-2732-6620
Jurjen van der SchansGlobal Health Unit, Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe World Health Organization supports both the screen-and-treat (ST) approach and the screen, triage and treat (STT) approach to cervical cancer screening using high-risk human papillomavirus (hrHPV) testing. For Uganda, the sequence of hrHPV-ST and hrHPV-STT could be similar, with visual inspection with acetic acid (VIA) after positive hrHPV tests in both. To consider potential tradeoffs (overtreatment in ST versus missed cancer cases in STT), we compared hrHPV-STT with VIA triage (STT-VIA), and STT with HPV 16/18 genotyping risk stratification, to hrHPV-ST for Uganda, in terms of overtreatment, cervical cancer incidence, and life years, for the general female population of Uganda.

methodsA microsimulation model of cervical cancer was adapted. Incremental benefit-harm ratios of STT were calculated as ratios of prevented overtreatment to reduced life years, and to increased cancer cases. Additional scenarios with 20% difference in intra- and inter-screening follow-up between ST and STT were modeled.

resultsBoth STT strategies resulted in life year losses on average compared to ST. STT-VIA prevented more overtreatment but led to increased cervical cancer incidence and life year losses. STT-G-VIA resulted in better harm-benefit ratios and additional costs. With better follow-up, STT prevented overtreatment and improved outcomes. DISCUSSION: For Uganda, the STT approach appears preferrable, if the screening sequences of hrHPV-based ST and STT are similar in practice. While VIA triage alone would reduce overtreatment the most, it could also result in more cancer cases. Risk stratification via genotyping could improve STT. Potential follow-up differences and resource availability should be considered by decision-makers when planning Uganda's hrHPV-based screening strategy.

Indexed as

Early Detection of CancerPapillomavirus InfectionsUterine Cervical NeoplasmsAdultFemaleHuman papillomavirus 16Human papillomavirus 18Human Papillomavirus VirusesHumansMass ScreeningMiddle AgedUganda

Identifiers

PMID39441790
PMCPMC11498676

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Registered trials

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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.