Evidence map›Paper›PMID 32923875›Full record

ArticleJCO precision oncology2020

Vulvar Squamous Cell Carcinoma: Comprehensive Genomic Profiling of HPV+ Versus HPV- Forms Reveals Distinct Sets of Potentially Actionable Molecular Targets.

Erik A Williams, Adrienne J Werth, Radwa Sharaf, Meagan Montesion, Ethan S Sokol, Dean C Pavlick, Molly McLaughlin-Drubin, Rachel Erlich, Helen Toma, Kevin Jon Williams and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in JCO precision oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

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  10. Molecular and microenvironmental landscapes of human papillomavirus-independent invasive squamous cell carcinoma of the vulva.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2025
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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

23 authors at 5 institutions in 1 country.

Erik A WilliamsFoundation Medicine, Cambridge, MA.
Adrienne J WerthDepartment of Obstetrics and Gynecology, Christiana Hospital, Newark, DE.
Radwa SharafFoundation Medicine, Cambridge, MA.
Meagan MontesionFoundation Medicine, Cambridge, MA.
Ethan S SokolFoundation Medicine, Cambridge, MA.
Dean C PavlickFoundation Medicine, Cambridge, MA.
Molly McLaughlin-DrubinFoundation Medicine, Cambridge, MA.
Rachel ErlichFoundation Medicine, Cambridge, MA.
Helen TomaDepartment of Obstetrics and Gynecology, Christiana Hospital, Newark, DE.
Kevin Jon WilliamsLewis Katz School of Medicine at Temple University, Department of Physiology, Department of Medicine, Philadelphia, PA.
Jeff M VenstromFoundation Medicine, Cambridge, MA.
Brian M AlexanderFoundation Medicine, Cambridge, MA.
Nikunj ShahFoundation Medicine, Cambridge, MA.
Natalie DanzigerFoundation Medicine, Cambridge, MA.
Amanda C HemmerichFoundation Medicine, Cambridge, MA.
Eric A SeversonFoundation Medicine, Cambridge, MA.
Jonathan Keith KillianFoundation Medicine, Cambridge, MA.
Douglas I LinFoundation Medicine, Cambridge, MA.
Jeffrey S RossFoundation Medicine, Cambridge, MA.
Julie Y TseFoundation Medicine, Cambridge, MA.
Shakti H RamkissoonFoundation Medicine, Cambridge, MA.
Mark C MochelDepartments of Pathology and Dermatology, Virginia Commonwealth University School of Medicine, Richmond, VA.
Julia A ElvinFoundation Medicine, Cambridge, MA.
Foundation Medicine (United States)Christiana Hospital · USTemple University · USVirginia Commonwealth University · USWake Forest University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeVulvar squamous cell carcinoma (vSCC) encompasses two predominant variants: one associated with detectable high-risk strains of human papillomavirus (hrHPV) and a second form often occurring in the context of chronic dermatitis in postmenopausal women. Genomic assessment of a large-scale cohort of patients with aggressive vSCC may identify distinct mutational signatures. MATERIALS AND

methodsTumor samples from a total of 280 patients with vSCC underwent hybridization capture with analysis of up to 406 cancer-related genes. Human papillomavirus (HPV) sequences were detected by de novo assembly of nonhuman sequencing reads and aligned to the RefSeq database. Immunohistochemistry for programmed death-ligand 1 (PD-L1) was assessed.

resultsOne hundred two of 280 vSCCs (36%) contained hrHPV sequences, predominantly HPV 16 (88%). The HPV-positive (HPV+) group was significantly younger (median age, 59

conclusionComprehensive molecular profiles of vSCC vary considerably with hrHPV status and may inform patient selection into clinical trials. Sixty-one percent of HPV+ vSCCs had a pathogenic alteration in the PI3K/mTOR pathway, whereas HPV- vSCCs showed alterations in

Identifiers

PMID32923875
PMCPMC7446361
OpenAlexW3034363035

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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.