Evidence map›Paper›PMID 39766115›Full record

ReviewCancers2024

Molecular Subtypes of Vulvar Squamous Cell Carcinoma: The Significance of HPV-Independent/p53 Wild Type.

Lars-Christian Horn, Christine E Brambs, Blake Gilks, Lien Hoang, Naveena Singh, Grit Gesine Ruth Hiller, Kathrin Hering, Jessica N McAlpine, Amy Jamieson, Mona Alfaraidi and 3 more

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Evaluation of HER2 and Nectin-4 Expression in Primary Vaginal Cancers.International journal of molecular sciences · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. 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

13 authors.

Lars-Christian HornDivision of Gynecologic, Breast and Perinatal Pathology, Institute of Pathology, University Hospital Leipzig, D-04103 Leipzig, Germany.ORCID 0000-0002-9775-4858
Christine E BrambsDepartment of Obstetrics and Gynecology, Kantonsspital Luzern, 6004 Luzern, Switzerland.ORCID 0000-0001-7682-2172
Blake GilksDepartment of Anatomical Pathology, Vancouver General Hospital, The University of British Columbia, Vancouver, BC V5Z 1M9, Canada.
Lien HoangDepartment of Anatomical Pathology, Vancouver General Hospital, The University of British Columbia, Vancouver, BC V5Z 1M9, Canada.
Naveena SinghDepartment of Anatomical Pathology, Vancouver General Hospital, The University of British Columbia, Vancouver, BC V5Z 1M9, Canada.
Grit Gesine Ruth HillerDivision of Gynecologic, Breast and Perinatal Pathology, Institute of Pathology, University Hospital Leipzig, D-04103 Leipzig, Germany.
Kathrin HeringDepartment of Radiotherapy and Radiation Oncology, University Hospital Leipzig, D-04103 Leipzig, Germany.
Jessica N McAlpineDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of British Columbia, Vancouver, BC V5Z 1M9, Canada.ORCID 0000-0001-6003-485X
Amy JamiesonDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, The University of British Columbia, Vancouver, BC V5Z 1M9, Canada.
Mona AlfaraidiDepartment of Anatomical Pathology, Vancouver General Hospital, The University of British Columbia, Vancouver, BC V5Z 1M9, Canada.
Bahriye AktasDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Institute of Trier, University Hospital Leipzig, D-04103 Leipzig, Germany.ORCID 0000-0002-5474-051X
Nadja DornhöferDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Institute of Trier, University Hospital Leipzig, D-04103 Leipzig, Germany.ORCID 0000-0003-0247-1095
Anne Kathrin HöhnDivision of Gynecologic, Breast and Perinatal Pathology, Institute of Pathology, University Hospital Leipzig, D-04103 Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vulvar carcinoma is a rare disease, meeting the criteria for a "rare cancer", but its incidence is increasing, especially in women <60 years of age. Squamous cell carcinoma (VSCC) accounts for the overwhelming majority of vulvar carcinomas and is the focus of this review. As with many cancers, the increased understanding of molecular events during tumorigenesis has led to the emergence of the molecular subclassification of VSCC, which is subclassified into tumors that arise secondary to high-risk human papillomavirus infection (HPV-associated, or HPVa) and those that arise independently of HPV (HPVi), most commonly in the setting of a chronic inflammatory condition of the vulvar skin. This latter group of HPVi VSCC arises in most cases secondary to mutations in

Indexed as

classificationhuman papillomavirusmolecularp16p53prognosisradiation therapysquamous cell carcinomasurgeryvulvar cancer

Identifiers

PMID39766115
PMCPMC11674125

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.