Evidence map›Paper›PMID 34862598›Full record

ArticleThe British journal of dermatology2022

Validation of four cutaneous squamous cell carcinoma staging systems using nationwide data.

Zoe Claire Venables, Selin Tokez, Loes M Hollestein, Antien L Mooyaart, Renate Ruth van den Bos, Brian Rous, Irene M Leigh, Tamar Nijsten, Marlies Wakkee

Open access · hybridAbstract read
In one paragraph

Article in The British journal of dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

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  13. Bridging the gap: From clinical intuition to structured cutaneous squamous cell carcinoma classification.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
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  15. Review
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  19. Using Gene Expression Profiling to Personalize Skin Cancer Management.The Journal of clinical and aesthetic dermatology · 2022
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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

9 authors at 4 institutions in 2 countries.

Zoe Claire VenablesDepartment of Dermatology, Norfolk and Norwich University Hospital, Norwich, NR4 7UY, UK.ORCID 0000-0002-9929-2693
Selin TokezDepartments of, Dermatology, Erasmus MC Cancer Institute.ORCID 0000-0002-1640-2368
Loes M HollesteinDepartments of, Dermatology, Erasmus MC Cancer Institute.ORCID 0000-0001-8922-6791
Antien L MooyaartPathology, Erasmus University Medical Center, PO Box 2040, Rotterdam, CA, 3000, the Netherlands.ORCID 0000-0001-9810-5780
Renate Ruth van den BosDepartments of, Dermatology, Erasmus MC Cancer Institute.ORCID 0000-0002-4011-5561
Brian RousPublic Health England, West Wing, Victoria House, Capital Park, Fulbourn, Cambridge, CB21 5XA, UK.ORCID 0000-0002-7619-461X
Irene M LeighBarts and the London School of Medicine and Dentistry, London, UK.ORCID 0000-0001-8536-6439
Tamar NijstenDepartments of, Dermatology, Erasmus MC Cancer Institute.ORCID 0000-0001-9940-2875
Marlies WakkeeDepartments of, Dermatology, Erasmus MC Cancer Institute.ORCID 0000-0001-8578-901X
Erasmus MC · NLFulbourn Hospital · GBNetherlands Comprehensive Cancer Organisation · NLNorfolk and Norwich University Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCutaneous squamous cell carcinoma (cSCC) is the second most common cancer worldwide with relatively low metastatic potential (2-5%). Developments in therapeutic options have highlighted the need to better identify high-risk patients who could benefit from closer surveillance, adjuvant therapies and baseline/follow-up imaging, while at the same time safely omitting low-risk patients from further follow-up. Controversy remains regarding the predictive performance of current cSCC staging systems and which methodology to adopt.

objectivesTo validate the performance of four cSCC staging systems [American Joint Committee on Cancer 8th edition (AJCC8), Brigham and Women's Hospital (BWH), Tübingen and Salamanca T3 refinement] in predicting metastasis using a nationwide cohort.

methodsA nested case-control study using data from the National Disease Registration Service, England, 2013-2015 was conducted. Metastatic cSCC cases were identified using an algorithm to identify all potential cases for manual review. These were 1 : 1 matched on follow-up time to nonmetastatic controls randomly selected from 2013. Staging systems were analysed for distinctiveness, homogeneity, monotonicity, specificity, positive predictive value (PPV), negative predictive value (NPV) and c-index.

resultsWe included 887 metastatic cSCC cases and 887 nonmetastatic cSCC controls. The BWH system showed the highest specificity [92.8%, 95% confidence interval (CI) 90.8-94.3%, PPV (13.2%, 95% CI 10.6-16.2) and c-index (0.84, 95% CI 0.82-0.86). The AJCC8 showed superior NPV (99.2%, 95% CI 99.2-99.3), homogeneity and monotonicity compared with the BWH and Tübingen diameter and thickness classifications (P < 0.001). Salamanca refinement did not show any improvement in AJCC8 T3 cSCC staging.

conclusionsWe validated four cSCC staging systems using the largest nationwide dataset of metastatic cSCC so far. Although the BWH system showed the highest overall discriminative ability, PPV was low for all staging systems, which shows the need for further improvement and refining of current cSCC staging systems.

Indexed as

Carcinoma, Squamous CellNeoplasms, Second PrimarySkin NeoplasmsCase-Control StudiesFemaleHumansNeoplasm Staging

Identifiers

PMID34862598
PMCPMC9315012
OpenAlexW3216880031

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.