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New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified
PURPOSE: HER2 signaling functional activity may be important to measure in addition to HER2 protein quantification when identifying patients eligible for HER2 therapies. A HER2 Signaling Function (CELx HSF) Test for HER2-negative patients uses patient’s live tumor cells on a biosensor to identify pa...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039866/ https://www.ncbi.nlm.nih.gov/pubmed/32036454 http://dx.doi.org/10.1007/s00432-020-03144-7 |
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author | MacNeil, Ian A. Burns, David J. Rich, Benjamin E. Soltani, Sajjad M. Kharbush, Samantha Osterhaus, Nicole G. Sullivan, Brian F. Hawkins, Douglas M. Pietruska, Jodie R. Laing, Lance G. |
author_facet | MacNeil, Ian A. Burns, David J. Rich, Benjamin E. Soltani, Sajjad M. Kharbush, Samantha Osterhaus, Nicole G. Sullivan, Brian F. Hawkins, Douglas M. Pietruska, Jodie R. Laing, Lance G. |
author_sort | MacNeil, Ian A. |
collection | PubMed |
description | PURPOSE: HER2 signaling functional activity may be important to measure in addition to HER2 protein quantification when identifying patients eligible for HER2 therapies. A HER2 Signaling Function (CELx HSF) Test for HER2-negative patients uses patient’s live tumor cells on a biosensor to identify patients with abnormally high HER2-related signaling (HSFs+) likely to respond to anti-HER2 therapies. METHODS: The CELx HSF test was employed to: (1) characterize the sensitivity and specificity of the test to detect abnormal levels of HER2 signaling; (2) evaluate the inhibitory effectiveness of five different anti-HER2 therapies; (3) assess the correlation between CELx HSF test detection of abnormal HER2 signaling and response to HER2 therapy using xenograft models; and (4) confirm the prevalence of abnormal HER2 signaling amongst HER2-negative breast cancer patients (HER2−/HSFs+). RESULTS: HER2−/HSFs+ breast cancer patient samples were identified and showed sensitivity to five approved anti-HER2 therapies. Xenograft studies using both HER2+ and HER2− cell lines confirmed that CELx HER2 signaling status better predicts HER2 inhibitor efficacy than HER2 receptor status. In a study of 114 HER2-negative breast tumor patient samples, 27 (23.7%; 95% CI = 17–32%) had abnormal HER2 signaling (HSFs+). A ROC curve constructed with this dataset projects the CELx HSF Test would have greater than 90% sensitivity and specificity to detect the HER2−/HSFs+ patient population. CONCLUSIONS: The CELx HSF test is a well-characterized functional biomarker assay capable of identifying dynamic HER2-driven signaling dysfunction in tumor cells from HER2-negative breast cancer patients. This test has demonstrated efficacy of various HER2 targeted therapies in live tumor cells from the HSFs+ population and correlated the test result to HER2 drug response in mouse xenograft studies. The proportion of HER2-negative breast cancer patients found to have abnormal HER2 signaling in a 114 patient sample study, 20–25%, is significant. A clinical trial to evaluate the efficacy of anti-HER2 therapies in this patient population is warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00432-020-03144-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7039866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70398662020-03-09 New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified MacNeil, Ian A. Burns, David J. Rich, Benjamin E. Soltani, Sajjad M. Kharbush, Samantha Osterhaus, Nicole G. Sullivan, Brian F. Hawkins, Douglas M. Pietruska, Jodie R. Laing, Lance G. J Cancer Res Clin Oncol Original Article – Cancer Research PURPOSE: HER2 signaling functional activity may be important to measure in addition to HER2 protein quantification when identifying patients eligible for HER2 therapies. A HER2 Signaling Function (CELx HSF) Test for HER2-negative patients uses patient’s live tumor cells on a biosensor to identify patients with abnormally high HER2-related signaling (HSFs+) likely to respond to anti-HER2 therapies. METHODS: The CELx HSF test was employed to: (1) characterize the sensitivity and specificity of the test to detect abnormal levels of HER2 signaling; (2) evaluate the inhibitory effectiveness of five different anti-HER2 therapies; (3) assess the correlation between CELx HSF test detection of abnormal HER2 signaling and response to HER2 therapy using xenograft models; and (4) confirm the prevalence of abnormal HER2 signaling amongst HER2-negative breast cancer patients (HER2−/HSFs+). RESULTS: HER2−/HSFs+ breast cancer patient samples were identified and showed sensitivity to five approved anti-HER2 therapies. Xenograft studies using both HER2+ and HER2− cell lines confirmed that CELx HER2 signaling status better predicts HER2 inhibitor efficacy than HER2 receptor status. In a study of 114 HER2-negative breast tumor patient samples, 27 (23.7%; 95% CI = 17–32%) had abnormal HER2 signaling (HSFs+). A ROC curve constructed with this dataset projects the CELx HSF Test would have greater than 90% sensitivity and specificity to detect the HER2−/HSFs+ patient population. CONCLUSIONS: The CELx HSF test is a well-characterized functional biomarker assay capable of identifying dynamic HER2-driven signaling dysfunction in tumor cells from HER2-negative breast cancer patients. This test has demonstrated efficacy of various HER2 targeted therapies in live tumor cells from the HSFs+ population and correlated the test result to HER2 drug response in mouse xenograft studies. The proportion of HER2-negative breast cancer patients found to have abnormal HER2 signaling in a 114 patient sample study, 20–25%, is significant. A clinical trial to evaluate the efficacy of anti-HER2 therapies in this patient population is warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00432-020-03144-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-02-08 2020 /pmc/articles/PMC7039866/ /pubmed/32036454 http://dx.doi.org/10.1007/s00432-020-03144-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article – Cancer Research MacNeil, Ian A. Burns, David J. Rich, Benjamin E. Soltani, Sajjad M. Kharbush, Samantha Osterhaus, Nicole G. Sullivan, Brian F. Hawkins, Douglas M. Pietruska, Jodie R. Laing, Lance G. New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified |
title | New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified |
title_full | New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified |
title_fullStr | New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified |
title_full_unstemmed | New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified |
title_short | New HER2-negative breast cancer subtype responsive to anti-HER2 therapy identified |
title_sort | new her2-negative breast cancer subtype responsive to anti-her2 therapy identified |
topic | Original Article – Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039866/ https://www.ncbi.nlm.nih.gov/pubmed/32036454 http://dx.doi.org/10.1007/s00432-020-03144-7 |
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