Evidence map›Paper›PMID 32203095›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2020

Major p53 immunohistochemical patterns in in situ and invasive squamous cell carcinomas of the vulva and correlation with TP53 mutation status.

Basile Tessier-Cloutier, Kim E Kortekaas, Emily Thompson, Jennifer Pors, Julia Chen, Julie Ho, Leah M Prentice, Melissa K McConechy, Christine Chow, Lily Proctor and 5 more

Open access · greenAbstract read
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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
14.7field-weighted citation impact, top 1% of its field
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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 187 citations in OpenAlex.

  1. European Society of Gynaecological Oncology Guidelines for the Management of Patients with Vulvar Cancer - Update 2023.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2023
    Guideline
  2. A Phase II Basket Trial of Dual Anti-CTLA-4 and Anti-PD-1 Blockade in Rare Tumors SWOG S1609: Vulvar Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  3. Article
  4. Article
  5. Article
  6. Vulvar Squamous Cell Carcinoma: Scientific Progress and Impacts to Pathology Practice.International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists · 2026
    Review
  7. Article
  8. Article
  9. Evaluation of HER2 and Nectin-4 Expression in Primary Vaginal Cancers.International journal of molecular sciences · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. IHC p53 Performance in NordiQC: Recalibration of IHC Assays is Needed.Applied immunohistochemistry & molecular morphology : AIMM · 2026
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

12 more citing papers are in PubMed but not listed here.

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

15 authors at 3 institutions in 2 countries.

Basile Tessier-CloutierDepartment of Anatomical Pathology, Vancouver General Hospital, Vancouver, BC, Canada.ORCID http://orcid.org/0000-0001-8739-3879
Kim E KortekaasDepartment of Obstetrics and Gynecology, Leiden University Medical Center, Leiden, The Netherlands.
Emily ThompsonDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Jennifer PorsDepartment of Anatomical Pathology, Vancouver General Hospital, Vancouver, BC, Canada.
Julia ChenDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Julie HoDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Leah M PrenticeContextual Genomics Inc., Vancouver, BC, Canada.
Melissa K McConechyContextual Genomics Inc., Vancouver, BC, Canada.
Christine ChowGenetic Pathology Evaluation Center (GPEC), Vancouver, BC, Canada.ORCID http://orcid.org/0000-0001-5098-5731
Lily ProctorDepartment of Gynecology and Obstetrics, Division of Gynecologic Oncology, University of British Columbia, Vancouver, BC, Canada.
Jessica N McAlpineDepartment of Gynecology and Obstetrics, Division of Gynecologic Oncology, University of British Columbia, Vancouver, BC, Canada.
David G HuntsmanDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
C Blake GilksDepartment of Anatomical Pathology, Vancouver General Hospital, Vancouver, BC, Canada.
Tjalling Bosse *Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Lynn N Hoang *Department of Anatomical Pathology, Vancouver General Hospital, Vancouver, BC, Canada. Lien.Hoang@vch.ca.
University of British Columbia · CALeiden University Medical Center · NLCentre for Advancing Health Outcomes · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent literature has shown that vulvar squamous cell carcinoma (VSCC) can be stratified into two prognostically relevant groups based on human papillomavirus (HPV) status. The prognostic value of p53 for further sub-stratification, particularly in the HPV-independent group, has not been agreed upon. This disagreement is likely due to tremendous variations in p53 immunohistochemical (IHC) interpretation. To address this problem, we sought to compare p53 IHC patterns with TP53 mutation status. We studied 61 VSCC (48 conventional VSCC, 2 VSCC with sarcomatoid features, and 11 verrucous carcinomas) and 42 in situ lesions (30 differentiated vulvar intraepithelial neoplasia [dVIN], 9 differentiated exophytic vulvar intraepithelial lesions [deVIL], and 3 high-grade squamous intraepithelial lesions or usual vulvar intraepithelial neoplasia [HSIL/uVIN]). IHC for p16 and p53, and sequencing of TP53 exons 4-9 were performed. HPV in situ hybridization (ISH) was performed in selected cases. We identified six major p53 IHC patterns, two wild-type patterns: (1) scattered, (2) mid-epithelial expression (with basal sparing), and four mutant patterns: (3) basal overexpression, (4) parabasal/diffuse overexpression, (5) absent, and (6) cytoplasmic expression. These IHC patterns were consistent with TP53 mutation status in 58/61 (95%) VSCC and 39/42 (93%) in situ lesions. Cases that exhibited strong scattered staining and those with a weak basal overexpression pattern could be easily confused. The mid-epithelial pattern was exclusively observed in p16-positive lesions; the basal and parabasal layers that had absent p53 staining, appeared to correlate with the cells that were positive for HPV-ISH. This study describes a pattern-based p53 IHC interpretation framework, which can be utilized as a surrogate marker for TP53 mutational status in both VSCC and vulvar in situ lesions.

Indexed as

Biomarkers, TumorCarcinoma, Squamous CellFemaleHumansImmunohistochemistryMutationTumor Suppressor Protein p53Vulvar NeoplasmsBiomarkers, TumorTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID32203095
OpenAlexW3010961770

What OpenQuestion holds

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Read underepoch 390

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.