Evidence map›Paper›PMID 40105043›Full record

ArticleInternational journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics2025

Improved cervical screening using HPV type restriction and cycle threshold limit setting with the AmpFire assay: A prospective screening cohort of women with and without HIV in Botswana.

Rebecca Luckett, Doreen Ramogola-Masire, Sikhulile Moyo, Annika Gompers, Anna Modest, Natasha Moraka, Thanolo Kashamba, Leabaneng Tawe, Farzad Noubary, Louise Kuhn and 7 more

Abstract read
In one paragraph

Article in International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Rebecca LuckettDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-1975-8837
Doreen Ramogola-MasireDepartment of Obstetrics and Gynecology, University of Botswana, Gaborone, Botswana.
Sikhulile MoyoBotswana Harvard Health Partnership, Gaborone, Botswana.
Annika GompersDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Anna ModestDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Natasha MorakaBotswana Harvard Health Partnership, Gaborone, Botswana.
Thanolo KashambaDepartment of Pathology, University of Botswana, Gaborone, Botswana.
Leabaneng TaweBotswana UPenn Partnership, Gaborone, Botswana.
Farzad NoubaryDepartment of Health Sciences, Northeastern University, Boston, Massachusetts, USA.
Louise KuhnDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York, USA.
Surbhi GroverDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Scott Dryden-PetersonBotswana Harvard Health Partnership, Gaborone, Botswana.
Greta DreyerDepartment of Obstetrics and Gynecology, University of Pretoria, Pretoria, South Africa.
Joseph MakhemaBotswana Harvard Health Partnership, Gaborone, Botswana.
Matthys H BothaDepartment of Obstetrics and Gynecology, Stellenbosch University, Cape Town, South Africa.
Michele R HackerDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Roger ShapiroBotswana Harvard Health Partnership, Gaborone, Botswana.

Funding

The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ARTHUR Y KIM · 2004 to 2026
$94.4M
Covid-19-related cervical cancer treatment interruption and role of neoadjuvant chemotherapyR01CA236546 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI DRYDEN-PETERSON, SCOTT · 2019 to 2023
$2.5M
Botswana CASCADE Clinical Trials SiteUG1CA275416 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Scott Dryden-Peterson, Doreen Ramogola-Masire · 2022 to 2026
$1.4M
Evaluation of triage strategies and screening intervals in a human papillomavirus based cervical cancer screening program in women living with human immunodeficiency virus in BotswanaK08CA271949 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Rebecca Luckett · 2022 to 2026
$1.3M
Viral Diversity an Innovative Biomarker for Refining Estimates of HIV IncidenceK43TW012350 · FIC · THE BOTSWANA HARVARD HEALTH PARTNERSHIP · PI Sikhulile Moyo · 2022 to 2026
$682k
FIC NIH HHS K43 TW012350FIC NIH HHS K43 TW012350-01NCI NIH HHS 1K08CA271949NCI NIH HHS K08 CA271949NCI NIH HHS R01 CA236546NCI NIH HHS UG1 CA275416NIAID NIH HHS P30 AI060354
6 · The paper itself

Abstract

objectiveThe aim of this study was to evaluate the performance of HPV type restriction and cycle threshold (Ct)-limit setting to optimize detection of cervical intraepithelial neoplasia (CIN) with primary HPV testing.

methodsBaseline cervical screening at time of entry into a prospective longitudinal cohort of women with and without HIV was conducted from February 2021 to July 2022 in Botswana. All women underwent HPV testing of 15 individual types using the AmpFire assay; all HPV-positive and a random subset of HPV negative had histopathology collected. Performance parameters of HPV type restriction groupings were calculated, and sensitivity by individual HPV type Ct-value limits were plotted.

resultsAmong 2964 women who underwent primary HPV screening, 1293 (43.6%) tested HPV-positive. Among women with HIV (WWH), HPV types 16/18/33 were associated with the greatest burden of CIN2+/CIN3+ (53%/56%). In WWH, grouping by HPV types separately reported in commercial assays (16/18/45) had low sensitivity (44% [CI: 36%-52%]) but high specificity (86% [CI: 84%-88%]) for CIN2+; 8-type HPV restriction (16/18/31/33/35/45/52/58) improved sensitivity (79% [CI: 72%-86%]) and maintained reasonable specificity (67% [CI: 65%-70%]) for CIN2+. Similar results were seen in women without HIV. Ct-limit setting for medium oncogenic HPV types (31,33,35,52,58) maintained a sensitivity of 72% in WWH while reducing over-detection of non-pathogenic HPV.

conclusionEight-type HPV restriction and Ct-limit setting are promising strategies for improving the performance of primary HPV screening. A potential strategy to improve 8-type HPV restriction would be to treat all with HPV 16/18/45; treat HPV 31/33/35/52/58 if below the type-specific Ct limit and repeat HPV testing in 1-year for other positive HPV results.

Indexed as

Early Detection of CancerHIV InfectionsMass ScreeningPapillomaviridaePapillomavirus InfectionsUterine Cervical DysplasiaUterine Cervical NeoplasmsAdultBotswanaFemaleHumansLongitudinal StudiesMiddle AgedProspective StudiesSensitivity and SpecificityYoung Adult8‐type HPV genotype restrictioncervical dysplasiacervical screeningCt‐valueHPV viral loadhuman immunodeficiency virus (HIV)human papillomavirus (HPV)low‐ and middle‐income countries (LMICs)

Identifiers

PMID40105043
PMCPMC12255922

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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.