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A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications

BACKGROUND: Lung cancer is the leading cause of cancer-related death worldwide. Surgical resection remains the definitive curative treatment for early-stage disease offering an overall 5-year survival rate of 62%. Despite careful case selection, a significant proportion of early-stage cancers relaps...

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Autores principales: Patel, Akshay J., Tan, Ti-Myen, Richter, Alex G., Naidu, Babu, Blackburn, Jonathan M., Middleton, Gary W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770460/
https://www.ncbi.nlm.nih.gov/pubmed/34728792
http://dx.doi.org/10.1038/s41416-021-01572-x
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author Patel, Akshay J.
Tan, Ti-Myen
Richter, Alex G.
Naidu, Babu
Blackburn, Jonathan M.
Middleton, Gary W.
author_facet Patel, Akshay J.
Tan, Ti-Myen
Richter, Alex G.
Naidu, Babu
Blackburn, Jonathan M.
Middleton, Gary W.
author_sort Patel, Akshay J.
collection PubMed
description BACKGROUND: Lung cancer is the leading cause of cancer-related death worldwide. Surgical resection remains the definitive curative treatment for early-stage disease offering an overall 5-year survival rate of 62%. Despite careful case selection, a significant proportion of early-stage cancers relapse aggressively within the first year post-operatively. Identification of these patients is key to accurate prognostication and understanding the biology that drives early relapse might open up potential novel adjuvant therapies. METHODS: We performed an unsupervised interrogation of >1600 serum-based autoantibody biomarkers using an iterative machine-learning algorithm. RESULTS: We identified a 13 biomarker signature that was highly predictive for survivorship in post-operative early-stage lung cancer; this outperforms currently used autoantibody biomarkers in solid cancers. Our results demonstrate significantly poor survivorship in high expressers of this biomarker signature with an overall 5-year survival rate of 7.6%. CONCLUSIONS: We anticipate that the data will lead to the development of an off-the-shelf prognostic panel and further that the oncogenic relevance of the proteins recognised in the panel may be a starting point for a new adjuvant therapy.
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spelling pubmed-87704602022-02-04 A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications Patel, Akshay J. Tan, Ti-Myen Richter, Alex G. Naidu, Babu Blackburn, Jonathan M. Middleton, Gary W. Br J Cancer Article BACKGROUND: Lung cancer is the leading cause of cancer-related death worldwide. Surgical resection remains the definitive curative treatment for early-stage disease offering an overall 5-year survival rate of 62%. Despite careful case selection, a significant proportion of early-stage cancers relapse aggressively within the first year post-operatively. Identification of these patients is key to accurate prognostication and understanding the biology that drives early relapse might open up potential novel adjuvant therapies. METHODS: We performed an unsupervised interrogation of >1600 serum-based autoantibody biomarkers using an iterative machine-learning algorithm. RESULTS: We identified a 13 biomarker signature that was highly predictive for survivorship in post-operative early-stage lung cancer; this outperforms currently used autoantibody biomarkers in solid cancers. Our results demonstrate significantly poor survivorship in high expressers of this biomarker signature with an overall 5-year survival rate of 7.6%. CONCLUSIONS: We anticipate that the data will lead to the development of an off-the-shelf prognostic panel and further that the oncogenic relevance of the proteins recognised in the panel may be a starting point for a new adjuvant therapy. Nature Publishing Group UK 2021-11-02 2022-02-01 /pmc/articles/PMC8770460/ /pubmed/34728792 http://dx.doi.org/10.1038/s41416-021-01572-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Patel, Akshay J.
Tan, Ti-Myen
Richter, Alex G.
Naidu, Babu
Blackburn, Jonathan M.
Middleton, Gary W.
A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications
title A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications
title_full A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications
title_fullStr A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications
title_full_unstemmed A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications
title_short A highly predictive autoantibody-based biomarker panel for prognosis in early-stage NSCLC with potential therapeutic implications
title_sort highly predictive autoantibody-based biomarker panel for prognosis in early-stage nsclc with potential therapeutic implications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770460/
https://www.ncbi.nlm.nih.gov/pubmed/34728792
http://dx.doi.org/10.1038/s41416-021-01572-x
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