Evidence map›Paper›PMID 42588614›Full record

ArticleCancers2026

HPV Genotype Landscape in Anal Squamous Cell Carcinoma Across Primary, Recurrent, and Metastatic Tumor Specimens.

Rose Seiberth, Hans Michael Kvasnicka, Tina Senff, David Brodmann, Florian Gebauer, Lars Bönicke, Daniel Gödde

Abstract read
In one paragraph

Article in Cancers, 2026. 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

7 authors.

Rose SeiberthDepartment of General, Visceral and Oncological Surgery, Helios University Hospital Wuppertal, University of Witten/Herdecke, Heusnerstraße 40, 42283 Wuppertal, Germany.ORCID 0000-0002-9051-6224
Hans Michael KvasnickaInstitute of Pathology and Molecular Pathology, Helios University Hospital Wuppertal, University of Witten/Herdecke, 42283 Wuppertal, Germany.ORCID 0000-0002-5450-4840
Tina SenffInstitute of Pathology and Molecular Pathology, Helios University Hospital Wuppertal, University of Witten/Herdecke, 42283 Wuppertal, Germany.ORCID 0000-0003-1578-8163
David BrodmannInstitute of Pathology and Molecular Pathology, Helios University Hospital Wuppertal, University of Witten/Herdecke, 42283 Wuppertal, Germany.
Florian GebauerDepartment of General, Visceral and Oncological Surgery, Helios University Hospital Wuppertal, University of Witten/Herdecke, Heusnerstraße 40, 42283 Wuppertal, Germany.
Lars BönickeDepartment of General, Visceral and Oncological Surgery, Helios University Hospital Wuppertal, University of Witten/Herdecke, Heusnerstraße 40, 42283 Wuppertal, Germany.ORCID 0000-0003-0441-0149
Daniel GöddeInstitute of Pathology and Molecular Pathology, Helios University Hospital Wuppertal, University of Witten/Herdecke, 42283 Wuppertal, Germany.ORCID 0000-0002-8430-1411

Funding

Helios Kliniken GmbH 2020-0076
6 · The paper itself

Abstract

BACKGROUND/

objectivesAnal squamous cell carcinoma (SCCA) is an HPV-driven malignancy with rising incidence, yet systematic HPV genotyping across recurrences and metastases is lacking. We characterized the complete HPV genotype distribution across the disease course.

methodsWe retrospectively analyzed 213 tumor specimens from 136 patients (82 female, 54 male) with histologically confirmed SCCA, spanning primary, recurrent, and metastatic disease (2009-2019 and from 2020 onwards). Patients contributed one or more specimens depending on the number of sampled disease events; specimens comprised 138 primary biopsies, 55 recurrence biopsies, 2 re-recurrence biopsies, and 18 distant metastases. HPV genotyping was conducted using a validated 28-type multiplex real-time PCR assay (Anyplex™ II HPV28, Seegene Inc.).

resultsHPV DNA was detected in 179/213 specimens (84.0%; 95% CI 78.9-88.7) and 125/136 patients (91.9%; 95% CI 86.8-96.3). Across 269 HPV type detections, 24 distinct types were identified, with HPV 16 predominating both per-specimen (90.5%) and per-detection (60.2%) values. Non-HPV-16/18 high-risk types accounted for one in four high-risk detections (54/219; 24.7%; 95% CI 19.4-30.8). HPV positivity differed significantly by specimen type: 90.6% in primary biopsies versus 70.9% in recurrences (

conclusionsSCCA harbors a substantially broader HPV type spectrum than previously recognized. One in four high-risk detections lies beyond HPV 16/18, and high-risk types other than HPV 16 were the sole high-risk genotype detected in individual metastatic specimens. HPV positivity rates are significantly lower across specimen types, while the metastatic type spectrum converges on a few high-risk genotypes. Broad-spectrum HPV genotyping beyond types 16 and 18 warrants adoption as standard practice in SCCA diagnostics and surveillance, and potential stratification for HPV-directed therapies.

Indexed as

anal squamous cell carcinomaAnyplex II HPV28co-infectionHPV genotypinghuman papillomavirusmetastasismultiplex PCRtumor recurrencetype diversity

Identifiers

PMID42588614
PMCPMC13465161

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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.