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dc.contributor.authorWang, Jen_US
dc.contributor.authorHarwood, CAen_US
dc.contributor.authorBailey, Een_US
dc.contributor.authorBewicke-Copley, Fen_US
dc.contributor.authorAnene, CAen_US
dc.contributor.authorThomson, Jen_US
dc.contributor.authorQamar, MJen_US
dc.contributor.authorLaban, Ren_US
dc.contributor.authorNourse, Cen_US
dc.contributor.authorSchoenherr, Cen_US
dc.contributor.authorTreanor-Taylor, Men_US
dc.contributor.authorHealy, Een_US
dc.contributor.authorLai, Cen_US
dc.contributor.authorCraig, Pen_US
dc.contributor.authorMoyes, Cen_US
dc.contributor.authorRickaby, Wen_US
dc.contributor.authorMartin, Jen_US
dc.contributor.authorProby, Cen_US
dc.contributor.authorInman, GJen_US
dc.contributor.authorLeigh, IMen_US
dc.date.accessioned2023-08-29T12:36:11Z
dc.date.available2023-08-01en_US
dc.date.issued2023-08-14en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/90263
dc.description.abstractBACKGROUND: Metastasis of cutaneous squamous cell carcinoma (cSCC) is uncommon. Current staging methods are reported to have sub-optimal performances in metastasis prediction. Accurate identification of patients with tumours at high risk of metastasis would have a significant impact on management. OBJECTIVE: To develop a robust and validated gene expression profile (GEP) signature for predicting primary cSCC metastatic risk using an unbiased whole transcriptome discovery-driven approach. METHODS: Archival formalin-fixed paraffin-embedded primary cSCC with perilesional normal tissue from 237 immunocompetent patients (151 non-metastasising and 86 metastasising) were collected retrospectively from four centres. TempO-seq was used to probe the whole transcriptome and machine learning algorithms were applied to derive predictive signatures, with a 3:1 split for training and testing datasets. RESULTS: A 20-gene prognostic model was developed and validated, with an accuracy of 86.0%, sensitivity of 85.7%, specificity of 86.1%, and positive predictive value of 78.3% in the testing set, providing more stable, accurate prediction than pathological staging systems. A linear predictor was also developed, significantly correlating with metastatic risk. LIMITATIONS: This was a retrospective 4-centre study and larger prospective multicentre studies are now required. CONCLUSION: The 20-gene signature prediction is accurate, with the potential to be incorporated into clinical workflows for cSCC.en_US
dc.languageengen_US
dc.relation.ispartofJ Am Acad Dermatolen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectCutaneous squamous cell carcinomaen_US
dc.subjectMachine learningen_US
dc.subjectMetastasisen_US
dc.subjectPrognosisen_US
dc.subjectRisk stratificationen_US
dc.subjectTranscriptomicsen_US
dc.titleTranscriptomic analysis of cutaneous squamous cell carcinoma reveals a multi-gene prognostic signature associated with metastasis.en_US
dc.typeArticle
dc.identifier.doi10.1016/j.jaad.2023.08.012en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37586461en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
dcterms.dateAccepted2023-08-01en_US


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States