Transcriptomic analysis of cutaneous squamous cell carcinoma reveals a multi-gene prognostic signature associated with metastasis
Transcriptomic analysis of cutaneous squamous cell carcinoma reveals a multi-gene prognostic signature associated with metastasis
Background: 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 tumors at high risk of metastasis would have a significant impact on management. Objective: To develop a robust and validated gene expression profile 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 nonmetastasizing and 86 metastasizing) were collected retrospectively from four centers. 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-center study and larger prospective multicenter studies are now required. Conclusion: The 20-gene signature prediction is accurate, with the potential to be incorporated into clinical workflows for cSCC.
cutaneous squamous cell carcinoma, machine learning, metastasis, prognosis, risk stratification, transcriptomics
1159-1166
Wang, Jun
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Harwood, Catherine A.
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Bailey, Emma
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Bewicke-Copley, Findlay
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Anene, Chinegu Anthony
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Thomson, Jason
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Qamar, Mah Jabeen
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Laban, Rhiannon
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Nourse, Craig
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Schoenherr, Christina
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Treanor-Taylor, Mairi
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Healy, Eugene
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Lai, Chester
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Craig, Paul
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Moyes, Colin
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Rickaby, William
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Martin, Joanne
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Proby, Charlotte
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Inman, Gareth J.
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Leigh, Irene M.
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December 2023
Wang, Jun
7b19868b-d14c-40fe-b441-b78b8a82e001
Harwood, Catherine A.
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Bailey, Emma
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Bewicke-Copley, Findlay
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Anene, Chinegu Anthony
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Thomson, Jason
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Qamar, Mah Jabeen
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Laban, Rhiannon
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Nourse, Craig
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Schoenherr, Christina
3d18b0dd-3536-47ba-84c9-eef87e158cd8
Treanor-Taylor, Mairi
5d50b99d-c134-4111-9568-9210254166fc
Healy, Eugene
400fc04d-f81a-474a-ae25-7ff894be0ebd
Lai, Chester
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Craig, Paul
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Moyes, Colin
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Rickaby, William
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Martin, Joanne
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Proby, Charlotte
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Inman, Gareth J.
5076ea97-8add-499e-b540-9d8d20a93826
Leigh, Irene M.
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Wang, Jun, Harwood, Catherine A., Bailey, Emma, Bewicke-Copley, Findlay, Anene, Chinegu Anthony, Thomson, Jason, Qamar, Mah Jabeen, Laban, Rhiannon, Nourse, Craig, Schoenherr, Christina, Treanor-Taylor, Mairi, Healy, Eugene, Lai, Chester, Craig, Paul, Moyes, Colin, Rickaby, William, Martin, Joanne, Proby, Charlotte, Inman, Gareth J. and Leigh, Irene M.
(2023)
Transcriptomic analysis of cutaneous squamous cell carcinoma reveals a multi-gene prognostic signature associated with metastasis.
Journal of the American Academy of Dermatology, 89 (6), .
(doi:10.1016/j.jaad.2023.08.012).
Abstract
Background: 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 tumors at high risk of metastasis would have a significant impact on management. Objective: To develop a robust and validated gene expression profile 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 nonmetastasizing and 86 metastasizing) were collected retrospectively from four centers. 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-center study and larger prospective multicenter studies are now required. Conclusion: The 20-gene signature prediction is accurate, with the potential to be incorporated into clinical workflows for cSCC.
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Sanofi paper 20-gene signature 2023 revised v1 clean accepted
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Accepted/In Press date: 1 August 2023
e-pub ahead of print date: 14 August 2023
Published date: December 2023
Additional Information:
Funding Information:
Funding sources: The research was funded by Sanofi-Regeneron as an investigator support award to IML with co-investigators JW and GJI.
Publisher Copyright:
© 2023 American Academy of Dermatology, Inc.
Keywords:
cutaneous squamous cell carcinoma, machine learning, metastasis, prognosis, risk stratification, transcriptomics
Identifiers
Local EPrints ID: 481535
URI: http://eprints.soton.ac.uk/id/eprint/481535
ISSN: 0190-9622
PURE UUID: 0a9999bc-9f04-41e1-bd07-9724e8d0bd39
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Date deposited: 31 Aug 2023 16:55
Last modified: 11 Apr 2024 16:59
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Contributors
Author:
Jun Wang
Author:
Catherine A. Harwood
Author:
Emma Bailey
Author:
Findlay Bewicke-Copley
Author:
Chinegu Anthony Anene
Author:
Jason Thomson
Author:
Mah Jabeen Qamar
Author:
Rhiannon Laban
Author:
Craig Nourse
Author:
Christina Schoenherr
Author:
Mairi Treanor-Taylor
Author:
Chester Lai
Author:
Paul Craig
Author:
Colin Moyes
Author:
William Rickaby
Author:
Joanne Martin
Author:
Charlotte Proby
Author:
Gareth J. Inman
Author:
Irene M. Leigh
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