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Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer

Recent studies showed the clinical utility of next-generation sequencing of urinary cell-free DNA (cfDNA) from patients with urothelial bladder cancer (UBC). In this study, we aimed to develop urinary cfDNA analysis by droplet digital PCR (ddPCR) as a high-throughput and rapid assay for UBC detectio...

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Autores principales: Hayashi, Yujiro, Fujita, Kazutoshi, Matsuzaki, Kyosuke, Eich, Marie-Lisa, Tomiyama, Eisuke, Matsushita, Makoto, Koh, Yoko, Nakano, Kosuke, Wang, Cong, Ishizuya, Yu, Kato, Taigo, Hatano, Koji, Kawashima, Atsunari, Ujike, Takeshi, Uemura, Motohide, Imamura, Ryoichi, Netto, George J., Nonomura, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250242/
https://www.ncbi.nlm.nih.gov/pubmed/32509577
http://dx.doi.org/10.3389/fonc.2020.00755
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author Hayashi, Yujiro
Fujita, Kazutoshi
Matsuzaki, Kyosuke
Eich, Marie-Lisa
Tomiyama, Eisuke
Matsushita, Makoto
Koh, Yoko
Nakano, Kosuke
Wang, Cong
Ishizuya, Yu
Kato, Taigo
Hatano, Koji
Kawashima, Atsunari
Ujike, Takeshi
Uemura, Motohide
Imamura, Ryoichi
Netto, George J.
Nonomura, Norio
author_facet Hayashi, Yujiro
Fujita, Kazutoshi
Matsuzaki, Kyosuke
Eich, Marie-Lisa
Tomiyama, Eisuke
Matsushita, Makoto
Koh, Yoko
Nakano, Kosuke
Wang, Cong
Ishizuya, Yu
Kato, Taigo
Hatano, Koji
Kawashima, Atsunari
Ujike, Takeshi
Uemura, Motohide
Imamura, Ryoichi
Netto, George J.
Nonomura, Norio
author_sort Hayashi, Yujiro
collection PubMed
description Recent studies showed the clinical utility of next-generation sequencing of urinary cell-free DNA (cfDNA) from patients with urothelial bladder cancer (UBC). In this study, we aimed to develop urinary cfDNA analysis by droplet digital PCR (ddPCR) as a high-throughput and rapid assay for UBC detection and prognosis. We analyzed urinary cfDNA of 202 samples from 2 cohorts. Test cohort was designed for investigating clinical utility of urinary cfDNA, and was composed of 74 samples from patients with UBC, and 52 samples of benign hematuria patients. Validation cohort was designed for validation and assessment of clinical utility comparing urinary cfDNA with UroVysion (Abbott, Illinois, USA), and was composed of 40 samples from patients with UBC, and 36 prospectively collected samples from patients under surveillance after surgery for urothelial carcinoma. We performed ddPCR analysis of hotspot gene mutations (TERT promoter and FGFR3). In the test cohort, the sensitivity of urinary cfDNA diagnosis was 68.9% (51/74) and the specificity was 100% in patients with UBC. The sensitivity increased to 85.9% when used in conjunction with urine cytology. In addition, patients with high TERT C228T allele frequency (≥14%) had significantly worse prognosis in bladder tumor recurrence than patients with low TERT C228T allele frequency or negative TERT C228T (p = 0.0322). In the validation cohort, the sensitivity of urinary cfDNA was 57.5% (23/40) and the specificity was 100% in UBC patients. The sensitivity of the combination of urine cytology with our hotspot analysis (77.5%) was higher than that of urine cytology with UroVysion (68.9%). In the post-surgical surveillance group, patients positive for the TERT C228T mutation had significantly worse prognosis for bladder tumor recurrence than mutation negative patients (p < 0.001). In conclusion, ddPCR analysis of urinary cfDNA is a simple and promising assay for the clinical setting, surpassing UroVysion for detection and prognosis determination in UBC.
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spelling pubmed-72502422020-06-05 Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer Hayashi, Yujiro Fujita, Kazutoshi Matsuzaki, Kyosuke Eich, Marie-Lisa Tomiyama, Eisuke Matsushita, Makoto Koh, Yoko Nakano, Kosuke Wang, Cong Ishizuya, Yu Kato, Taigo Hatano, Koji Kawashima, Atsunari Ujike, Takeshi Uemura, Motohide Imamura, Ryoichi Netto, George J. Nonomura, Norio Front Oncol Oncology Recent studies showed the clinical utility of next-generation sequencing of urinary cell-free DNA (cfDNA) from patients with urothelial bladder cancer (UBC). In this study, we aimed to develop urinary cfDNA analysis by droplet digital PCR (ddPCR) as a high-throughput and rapid assay for UBC detection and prognosis. We analyzed urinary cfDNA of 202 samples from 2 cohorts. Test cohort was designed for investigating clinical utility of urinary cfDNA, and was composed of 74 samples from patients with UBC, and 52 samples of benign hematuria patients. Validation cohort was designed for validation and assessment of clinical utility comparing urinary cfDNA with UroVysion (Abbott, Illinois, USA), and was composed of 40 samples from patients with UBC, and 36 prospectively collected samples from patients under surveillance after surgery for urothelial carcinoma. We performed ddPCR analysis of hotspot gene mutations (TERT promoter and FGFR3). In the test cohort, the sensitivity of urinary cfDNA diagnosis was 68.9% (51/74) and the specificity was 100% in patients with UBC. The sensitivity increased to 85.9% when used in conjunction with urine cytology. In addition, patients with high TERT C228T allele frequency (≥14%) had significantly worse prognosis in bladder tumor recurrence than patients with low TERT C228T allele frequency or negative TERT C228T (p = 0.0322). In the validation cohort, the sensitivity of urinary cfDNA was 57.5% (23/40) and the specificity was 100% in UBC patients. The sensitivity of the combination of urine cytology with our hotspot analysis (77.5%) was higher than that of urine cytology with UroVysion (68.9%). In the post-surgical surveillance group, patients positive for the TERT C228T mutation had significantly worse prognosis for bladder tumor recurrence than mutation negative patients (p < 0.001). In conclusion, ddPCR analysis of urinary cfDNA is a simple and promising assay for the clinical setting, surpassing UroVysion for detection and prognosis determination in UBC. Frontiers Media S.A. 2020-05-19 /pmc/articles/PMC7250242/ /pubmed/32509577 http://dx.doi.org/10.3389/fonc.2020.00755 Text en Copyright © 2020 Hayashi, Fujita, Matsuzaki, Eich, Tomiyama, Matsushita, Koh, Nakano, Wang, Ishizuya, Kato, Hatano, Kawashima, Ujike, Uemura, Imamura, Netto and Nonomura. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Hayashi, Yujiro
Fujita, Kazutoshi
Matsuzaki, Kyosuke
Eich, Marie-Lisa
Tomiyama, Eisuke
Matsushita, Makoto
Koh, Yoko
Nakano, Kosuke
Wang, Cong
Ishizuya, Yu
Kato, Taigo
Hatano, Koji
Kawashima, Atsunari
Ujike, Takeshi
Uemura, Motohide
Imamura, Ryoichi
Netto, George J.
Nonomura, Norio
Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer
title Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer
title_full Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer
title_fullStr Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer
title_full_unstemmed Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer
title_short Clinical Significance of Hotspot Mutation Analysis of Urinary Cell-Free DNA in Urothelial Bladder Cancer
title_sort clinical significance of hotspot mutation analysis of urinary cell-free dna in urothelial bladder cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250242/
https://www.ncbi.nlm.nih.gov/pubmed/32509577
http://dx.doi.org/10.3389/fonc.2020.00755
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