Evidence map›Paper›PMID 42403920›Full record

ArticleThe Lancet regional health. Europe2026

Primary Human Papillomavirus Screening Versus Cytology for Detection of Cervical Intraepithelial Neoplasia Grade 2 or Higher in Poland: a Parallel-Group, Randomized Controlled Trial.

Andrzej Nowakowski, Anna Macios, Patrycja Glinska, Aneta Chmielewska, Beata Janik, Ilona Jędrzejewska, Alicja Klimiuk, Ewa Chmielik, Piotr Bobkiewicz, Ewa Kapuśniak and 4 more

Abstract read
In one paragraph

Article in The Lancet regional health. Europe, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Andrzej NowakowskiDepartment of Cancer Prevention, Central Coordinating Centre for Cervical Cancer Screening Program, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Anna MaciosDepartment of Cancer Prevention, Central Coordinating Centre for Cervical Cancer Screening Program, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Patrycja GlinskaDepartment of Oncology Diagnostics, Cardio-Oncology, and Palliative Medicine, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Aneta ChmielewskaDepartment of Cancer Prevention, Central Coordinating Centre for Cervical Cancer Screening Program, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Beata JanikDepartment of Cancer Prevention, Central Coordinating Centre for Cervical Cancer Screening Program, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Ilona JędrzejewskaDepartment of Cancer Prevention, Central Coordinating Centre for Cervical Cancer Screening Program, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Alicja KlimiukDepartment of Cancer Prevention, Central Coordinating Centre for Cervical Cancer Screening Program, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
Ewa ChmielikDepartment of Cancer Pathology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, Poland.
Piotr BobkiewiczALAB Plus Pathology Laboratory Ltd., Warsaw, Poland.
Ewa KapuśniakMedical Centre FEMINA, Katowice, Poland.
Jacek PodolskiNon-public Health Care Facility Meditest - Medical Diagnostics, Szczecin, Poland.
Ewa ProkuratMedical and Diagnostic Centre, Siedlce, Poland.
Marc ArbynUnit of Cancer Epidemiology, Belgian Cancer Centre, Scientific Institute of Public Health, Brussels, Belgium.
Michal Filip KamińskiDepartment of Oncological Gastroenterology, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: 2025 European guidelines recommended transition from cytology to HPV-based cervical cancer screening. We compared both strategies in a pilot in Poland. Methods: Eligible, consenting women aged 30-59 years underwent centralized 1:1 randomization to HPV-testing or cytology (HPV or cytology arm, respectively) in 30-39, 40-49, and 50-59 years age strata in 27 clinics. Arm assignment was unblinded. HPV positive samples underwent liquid-based cytology (LBC) triage. If normal, another LBC was performed in six months. Abnormal LBC triggered colposcopy. If both LBCs were normal, p16/Ki-67 immunocytochemistry and Findings: Between 28 October 2019 and 31 December 2022, 16,795 and 16,707 women underwent primary HPV or cytological testing, respectively. 702/16,795 (4.2%; 95% CI: 3.9%-4.5%) and 499/16,707 women (3.0%; 95% CI: 2.7%-3.3%), were referred for colposcopy in the HPV and cytology arm, respectively (RR = 1.40; 95% CI: 1.25-1.57). CIN2+ was detected in 137 women (0.82%; 95% CI: 0.69-0.96%) and in 71 women (0.42%; 95% CI: 0.34-0.54%; OR = 1.93; 95% CI: 1.34-2.77), while CIN grade 3 or worse (CIN3+) was detected in 69 women (0.41%; 95% CI: 0.32%-0.52%) and in 35 women (0.21%; 95% CI: 0.15%-0.29%; OR = 1.99; 95% CI: 1.16-3.42) in the HPV and cytology arm, respectively. In HPV positive women with two normal LBCs immunocytochemistry and methylation detected 4/9 (44.4%) and 7/9 (77.8%) CIN2+ cases, respectively. Interpretation: HPV-based screening may almost double CIN2+ detection compared to cytology. It however yields more positive screening results and colposcopies. Smooth transition from cytology to HPV-based screening requires proper triage strategies and additional colposcopy services. Methylation seems to detect more CIN2+ than immunocytochemistry in HPV positive women with two normal LBCs. Funding: Polish Ministry of Health.

Indexed as

Cervical cancer screeningHPV testing efficacyPrimary HPV testing

Identifiers

PMID42403920
PMCPMC13330258

What OpenQuestion holds

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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.