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Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype

Background: LIV1 is a transmembrane protein that may become a new therapeutic target through the development of antibody–drug conjugates (ADCs). Few studies are available regarding the assessment of LIV1 expression in clinical breast cancer (BC) samples. Methods: We analyzed LIV1 mRNA expression in...

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Autores principales: de Nonneville, Alexandre, Finetti, Pascal, Boudin, Laurys, Denicolaï, Emilie, Birnbaum, Daniel, Mamessier, Emilie, Bertucci, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058875/
https://www.ncbi.nlm.nih.gov/pubmed/36986799
http://dx.doi.org/10.3390/pharmaceutics15030938
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author de Nonneville, Alexandre
Finetti, Pascal
Boudin, Laurys
Denicolaï, Emilie
Birnbaum, Daniel
Mamessier, Emilie
Bertucci, François
author_facet de Nonneville, Alexandre
Finetti, Pascal
Boudin, Laurys
Denicolaï, Emilie
Birnbaum, Daniel
Mamessier, Emilie
Bertucci, François
author_sort de Nonneville, Alexandre
collection PubMed
description Background: LIV1 is a transmembrane protein that may become a new therapeutic target through the development of antibody–drug conjugates (ADCs). Few studies are available regarding the assessment of LIV1 expression in clinical breast cancer (BC) samples. Methods: We analyzed LIV1 mRNA expression in 8982 primary BC. We searched for correlations between LIV1 expression and clinicopathological data, including disease-free survival (DFS), overall survival (OS), pathological complete response to chemotherapy (pCR), and potential vulnerability and actionability to anti-cancer drugs used or under development in BC. Analyses were performed in the whole population and each molecular subtype separately. Results: LIV1 expression was associated with good-prognosis features and with longer DFS and OS in multivariate analysis. However, patients with high LIV1 expression displayed a lower pCR rate than patients with low expression after anthracycline-based neoadjuvant chemotherapy, including in multivariate analysis adjusted on grade and molecular subtypes. LIV1-high tumors were associated with higher probabilities of sensitivity to hormone therapy and CDK4/6 inhibitors and lower probabilities of sensitivity to immune-checkpoint inhibitors and PARP inhibitors. These observations were different according to the molecular subtypes when analyzed separately. Conclusions: These results may provide novel insights into the clinical development and use of LIV1-targeted ADCs by identifying prognostic and predictive value of LIV1 expression in each molecular subtype and associated vulnerability to other systemic therapies.
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spelling pubmed-100588752023-03-30 Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype de Nonneville, Alexandre Finetti, Pascal Boudin, Laurys Denicolaï, Emilie Birnbaum, Daniel Mamessier, Emilie Bertucci, François Pharmaceutics Article Background: LIV1 is a transmembrane protein that may become a new therapeutic target through the development of antibody–drug conjugates (ADCs). Few studies are available regarding the assessment of LIV1 expression in clinical breast cancer (BC) samples. Methods: We analyzed LIV1 mRNA expression in 8982 primary BC. We searched for correlations between LIV1 expression and clinicopathological data, including disease-free survival (DFS), overall survival (OS), pathological complete response to chemotherapy (pCR), and potential vulnerability and actionability to anti-cancer drugs used or under development in BC. Analyses were performed in the whole population and each molecular subtype separately. Results: LIV1 expression was associated with good-prognosis features and with longer DFS and OS in multivariate analysis. However, patients with high LIV1 expression displayed a lower pCR rate than patients with low expression after anthracycline-based neoadjuvant chemotherapy, including in multivariate analysis adjusted on grade and molecular subtypes. LIV1-high tumors were associated with higher probabilities of sensitivity to hormone therapy and CDK4/6 inhibitors and lower probabilities of sensitivity to immune-checkpoint inhibitors and PARP inhibitors. These observations were different according to the molecular subtypes when analyzed separately. Conclusions: These results may provide novel insights into the clinical development and use of LIV1-targeted ADCs by identifying prognostic and predictive value of LIV1 expression in each molecular subtype and associated vulnerability to other systemic therapies. MDPI 2023-03-14 /pmc/articles/PMC10058875/ /pubmed/36986799 http://dx.doi.org/10.3390/pharmaceutics15030938 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Nonneville, Alexandre
Finetti, Pascal
Boudin, Laurys
Denicolaï, Emilie
Birnbaum, Daniel
Mamessier, Emilie
Bertucci, François
Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype
title Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype
title_full Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype
title_fullStr Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype
title_full_unstemmed Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype
title_short Prognostic and Predictive Value of LIV1 Expression in Early Breast Cancer and by Molecular Subtype
title_sort prognostic and predictive value of liv1 expression in early breast cancer and by molecular subtype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058875/
https://www.ncbi.nlm.nih.gov/pubmed/36986799
http://dx.doi.org/10.3390/pharmaceutics15030938
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