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Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer

INTRODUCTION: Here we describe the development of a protein immunofluorescent assay for the detection of nuclear-localized androgen receptor variant 7 (AR-V7) protein within circulating tumor cells (CTCs) identified in patient blood samples. Used in the clinic, the test result serves as a validated...

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Autores principales: Lu, David, Krupa, Rachel, Harvey, Melissa, Graf, Ryon P., Schreiber, Nicole, Barnett, Ethan, Carbone, Emily, Jendrisak, Adam, Gill, Audrey, Orr, Sarah, Scher, Howard I., Schonhoft, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AboutScience 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951184/
https://www.ncbi.nlm.nih.gov/pubmed/33717359
http://dx.doi.org/10.33393/jcb.2020.2163
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author Lu, David
Krupa, Rachel
Harvey, Melissa
Graf, Ryon P.
Schreiber, Nicole
Barnett, Ethan
Carbone, Emily
Jendrisak, Adam
Gill, Audrey
Orr, Sarah
Scher, Howard I.
Schonhoft, Joseph D.
author_facet Lu, David
Krupa, Rachel
Harvey, Melissa
Graf, Ryon P.
Schreiber, Nicole
Barnett, Ethan
Carbone, Emily
Jendrisak, Adam
Gill, Audrey
Orr, Sarah
Scher, Howard I.
Schonhoft, Joseph D.
author_sort Lu, David
collection PubMed
description INTRODUCTION: Here we describe the development of a protein immunofluorescent assay for the detection of nuclear-localized androgen receptor variant 7 (AR-V7) protein within circulating tumor cells (CTCs) identified in patient blood samples. Used in the clinic, the test result serves as a validated biomarker of futility for patients with progressing metastatic castration-resistant prostate cancer (mCRPC) who are treated with androgen receptor targeted therapies (AATT) in whom nuclear-localized AR-V7 CTCs are identified and have received level 2A evidence in the 2019 National Cancer Center Network (NCCN) guidelines (v1.0). METHODS: Assay development was completed on the Epic Sciences rare cell detection platform using control cell lines of known AR-V7 status and clinical testing of mCRPC patient samples obtained at the decision point in management. RESULTS AND CONCLUSIONS: Using these samples, all assay parameters, scoring criteria, and clinical cutoffs for positivity were prospectively selected and locked. After assay lock, blinded clinical validation testing was initiated on multiple, independent, clinical cohorts as reported by Scher et al (JAMA Oncol. 2016;2:1441-1449; JAMA Oncol. 2018;4:1179-1186) and Armstrong et al (J Clin Oncol. 2019;37:1120-1129).
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spelling pubmed-79511842021-03-12 Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer Lu, David Krupa, Rachel Harvey, Melissa Graf, Ryon P. Schreiber, Nicole Barnett, Ethan Carbone, Emily Jendrisak, Adam Gill, Audrey Orr, Sarah Scher, Howard I. Schonhoft, Joseph D. J Circ Biomark Original Research Article INTRODUCTION: Here we describe the development of a protein immunofluorescent assay for the detection of nuclear-localized androgen receptor variant 7 (AR-V7) protein within circulating tumor cells (CTCs) identified in patient blood samples. Used in the clinic, the test result serves as a validated biomarker of futility for patients with progressing metastatic castration-resistant prostate cancer (mCRPC) who are treated with androgen receptor targeted therapies (AATT) in whom nuclear-localized AR-V7 CTCs are identified and have received level 2A evidence in the 2019 National Cancer Center Network (NCCN) guidelines (v1.0). METHODS: Assay development was completed on the Epic Sciences rare cell detection platform using control cell lines of known AR-V7 status and clinical testing of mCRPC patient samples obtained at the decision point in management. RESULTS AND CONCLUSIONS: Using these samples, all assay parameters, scoring criteria, and clinical cutoffs for positivity were prospectively selected and locked. After assay lock, blinded clinical validation testing was initiated on multiple, independent, clinical cohorts as reported by Scher et al (JAMA Oncol. 2016;2:1441-1449; JAMA Oncol. 2018;4:1179-1186) and Armstrong et al (J Clin Oncol. 2019;37:1120-1129). AboutScience 2020-10-23 /pmc/articles/PMC7951184/ /pubmed/33717359 http://dx.doi.org/10.33393/jcb.2020.2163 Text en Copyright © 2020, The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/© 2020 The Authors. This article is published by AboutScience and licensed under Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). Any commercial use is not permitted and is subject to Publisher’s permissions. Full information is available at www.aboutscience.eu (http://www.aboutscience.eu)
spellingShingle Original Research Article
Lu, David
Krupa, Rachel
Harvey, Melissa
Graf, Ryon P.
Schreiber, Nicole
Barnett, Ethan
Carbone, Emily
Jendrisak, Adam
Gill, Audrey
Orr, Sarah
Scher, Howard I.
Schonhoft, Joseph D.
Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer
title Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer
title_full Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer
title_fullStr Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer
title_full_unstemmed Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer
title_short Development of an immunofluorescent AR-V7 circulating tumor cell assay – A blood-based test for men with metastatic prostate cancer
title_sort development of an immunofluorescent ar-v7 circulating tumor cell assay – a blood-based test for men with metastatic prostate cancer
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951184/
https://www.ncbi.nlm.nih.gov/pubmed/33717359
http://dx.doi.org/10.33393/jcb.2020.2163
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