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Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer

Muscle Invasive Bladder Cancer (MIBC) has a poor prognosis. Whilst patients can achieve a 6% improvement in overall survival with Neo-Adjuvant Chemotherapy (NAC), many do not respond. Body fluid mutant DNA (mutDNA) may allow non-invasive identification of treatment failure. We collected 248 liquid b...

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Autores principales: Patel, K. M., van der Vos, K. E., Smith, C. G., Mouliere, F., Tsui, D., Morris, J., Chandrananda, D., Marass, F., van den Broek, D., Neal, D. E., Gnanapragasam, V. J., Forshew, T., van Rhijn, B. W., Massie, C. E., Rosenfeld, N., van der Heijden, M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514073/
https://www.ncbi.nlm.nih.gov/pubmed/28717136
http://dx.doi.org/10.1038/s41598-017-05623-3
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author Patel, K. M.
van der Vos, K. E.
Smith, C. G.
Mouliere, F.
Tsui, D.
Morris, J.
Chandrananda, D.
Marass, F.
van den Broek, D.
Neal, D. E.
Gnanapragasam, V. J.
Forshew, T.
van Rhijn, B. W.
Massie, C. E.
Rosenfeld, N.
van der Heijden, M. S.
author_facet Patel, K. M.
van der Vos, K. E.
Smith, C. G.
Mouliere, F.
Tsui, D.
Morris, J.
Chandrananda, D.
Marass, F.
van den Broek, D.
Neal, D. E.
Gnanapragasam, V. J.
Forshew, T.
van Rhijn, B. W.
Massie, C. E.
Rosenfeld, N.
van der Heijden, M. S.
author_sort Patel, K. M.
collection PubMed
description Muscle Invasive Bladder Cancer (MIBC) has a poor prognosis. Whilst patients can achieve a 6% improvement in overall survival with Neo-Adjuvant Chemotherapy (NAC), many do not respond. Body fluid mutant DNA (mutDNA) may allow non-invasive identification of treatment failure. We collected 248 liquid biopsy samples including plasma, cell pellet (UCP) and supernatant (USN) from spun urine, from 17 patients undergoing NAC. We assessed single nucleotide variants and copy number alterations in mutDNA using Tagged-Amplicon- and shallow Whole Genome- Sequencing. MutDNA was detected in 35.3%, 47.1% and 52.9% of pre-NAC plasma, UCP and USN samples respectively, and urine samples contained higher levels of mutDNA (p = <0.001). Longitudinal mutDNA demonstrated tumour evolution under the selective pressure of NAC e.g. in one case, urine analysis tracked two distinct clones with contrasting treatment sensitivity. Of note, persistence of mutDNA detection during NAC predicted disease recurrence (p = 0.003), emphasising its potential as an early biomarker for chemotherapy response.
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spelling pubmed-55140732017-07-19 Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer Patel, K. M. van der Vos, K. E. Smith, C. G. Mouliere, F. Tsui, D. Morris, J. Chandrananda, D. Marass, F. van den Broek, D. Neal, D. E. Gnanapragasam, V. J. Forshew, T. van Rhijn, B. W. Massie, C. E. Rosenfeld, N. van der Heijden, M. S. Sci Rep Article Muscle Invasive Bladder Cancer (MIBC) has a poor prognosis. Whilst patients can achieve a 6% improvement in overall survival with Neo-Adjuvant Chemotherapy (NAC), many do not respond. Body fluid mutant DNA (mutDNA) may allow non-invasive identification of treatment failure. We collected 248 liquid biopsy samples including plasma, cell pellet (UCP) and supernatant (USN) from spun urine, from 17 patients undergoing NAC. We assessed single nucleotide variants and copy number alterations in mutDNA using Tagged-Amplicon- and shallow Whole Genome- Sequencing. MutDNA was detected in 35.3%, 47.1% and 52.9% of pre-NAC plasma, UCP and USN samples respectively, and urine samples contained higher levels of mutDNA (p = <0.001). Longitudinal mutDNA demonstrated tumour evolution under the selective pressure of NAC e.g. in one case, urine analysis tracked two distinct clones with contrasting treatment sensitivity. Of note, persistence of mutDNA detection during NAC predicted disease recurrence (p = 0.003), emphasising its potential as an early biomarker for chemotherapy response. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514073/ /pubmed/28717136 http://dx.doi.org/10.1038/s41598-017-05623-3 Text en © The Author(s) 2017 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/.
spellingShingle Article
Patel, K. M.
van der Vos, K. E.
Smith, C. G.
Mouliere, F.
Tsui, D.
Morris, J.
Chandrananda, D.
Marass, F.
van den Broek, D.
Neal, D. E.
Gnanapragasam, V. J.
Forshew, T.
van Rhijn, B. W.
Massie, C. E.
Rosenfeld, N.
van der Heijden, M. S.
Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer
title Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer
title_full Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer
title_fullStr Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer
title_full_unstemmed Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer
title_short Association Of Plasma And Urinary Mutant DNA With Clinical Outcomes In Muscle Invasive Bladder Cancer
title_sort association of plasma and urinary mutant dna with clinical outcomes in muscle invasive bladder cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514073/
https://www.ncbi.nlm.nih.gov/pubmed/28717136
http://dx.doi.org/10.1038/s41598-017-05623-3
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