Prognostic implication of TERT promoter mutation and circulating tumor cells in muscle-invasive bladder cancer
Purpose Current clinical prognostic factors are not accurate enough to identify and monitor those muscle-invasive bladder cancer (MIBC) patients at high risk of progression after radical cystectomy (RC). Here, we determined genetic alterations in the tumor and circulating tumor cell (CTC) enumeratio...
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Veröffentlicht in: | World journal of urology 2022-08, Vol.40 (8), p.2033-2039 |
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container_title | World journal of urology |
container_volume | 40 |
creator | Carrasco, Raquel Ingelmo-Torres, Mercedes Gómez, Ascensión Roldán, Fiorella L. Segura, Natalia Ribal, María José Alcaraz, Antonio Izquierdo, Laura Mengual, Lourdes |
description | Purpose
Current clinical prognostic factors are not accurate enough to identify and monitor those muscle-invasive bladder cancer (MIBC) patients at high risk of progression after radical cystectomy (RC). Here, we determined genetic alterations in the tumor and circulating tumor cell (CTC) enumeration to find biomarkers useful for the management of MIBC after RC.
Methods
Thirty-nine MIBC patients undergoing RC were included. Tumoral tissue DNA was analyzed by next generation sequencing. CTCs were isolated from blood collected before RC and one, four and 12 months later.
Results
Sixteen (41%) patients progressed in a median time of 8.5 months and 11 (69%) of these patients harbored the
TERT
c.-124C > T mutation. All progressive patients harboring the
TERT
c.-124C > T mutation presented a significant increase in CTC number 12 months after RC compared to those without the mutation. Additionally, CTC number at 12 months was identified as an independent prognostic biomarker for tumor progression and cancer specific survival (CSS). Ten (63%) progressive patients showed an increment of CTC number with a median anticipation period of four months compared with imaging techniques.
Conclusions
The
TERT
c.-124C > T mutation could be considered a biomarker of aggressivity. CTC enumeration is a useful tool for identifying MIBC patients at high risk of progression and CSS after RC and for detecting tumor progression earlier than imaging techniques. |
doi_str_mv | 10.1007/s00345-022-04061-9 |
format | Article |
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Current clinical prognostic factors are not accurate enough to identify and monitor those muscle-invasive bladder cancer (MIBC) patients at high risk of progression after radical cystectomy (RC). Here, we determined genetic alterations in the tumor and circulating tumor cell (CTC) enumeration to find biomarkers useful for the management of MIBC after RC.
Methods
Thirty-nine MIBC patients undergoing RC were included. Tumoral tissue DNA was analyzed by next generation sequencing. CTCs were isolated from blood collected before RC and one, four and 12 months later.
Results
Sixteen (41%) patients progressed in a median time of 8.5 months and 11 (69%) of these patients harbored the
TERT
c.-124C > T mutation. All progressive patients harboring the
TERT
c.-124C > T mutation presented a significant increase in CTC number 12 months after RC compared to those without the mutation. Additionally, CTC number at 12 months was identified as an independent prognostic biomarker for tumor progression and cancer specific survival (CSS). Ten (63%) progressive patients showed an increment of CTC number with a median anticipation period of four months compared with imaging techniques.
Conclusions
The
TERT
c.-124C > T mutation could be considered a biomarker of aggressivity. CTC enumeration is a useful tool for identifying MIBC patients at high risk of progression and CSS after RC and for detecting tumor progression earlier than imaging techniques.</description><identifier>ISSN: 1433-8726</identifier><identifier>ISSN: 0724-4983</identifier><identifier>EISSN: 1433-8726</identifier><identifier>DOI: 10.1007/s00345-022-04061-9</identifier><identifier>PMID: 35713686</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biomarkers ; Bladder cancer ; Cancer ; Enumeration ; Invasiveness ; Medical prognosis ; Medicine ; Medicine & Public Health ; Mutation ; Nephrology ; Next-generation sequencing ; Oncology ; Original ; Original Article ; Patients ; Tumor cells ; Urology</subject><ispartof>World journal of urology, 2022-08, Vol.40 (8), p.2033-2039</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c566t-3e350faa83c7b4149baab8142cfaf0dcf133b44152bbeac32b23b26f87e8d0163</citedby><cites>FETCH-LOGICAL-c566t-3e350faa83c7b4149baab8142cfaf0dcf133b44152bbeac32b23b26f87e8d0163</cites><orcidid>0000-0001-6015-2987</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00345-022-04061-9$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00345-022-04061-9$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Carrasco, Raquel</creatorcontrib><creatorcontrib>Ingelmo-Torres, Mercedes</creatorcontrib><creatorcontrib>Gómez, Ascensión</creatorcontrib><creatorcontrib>Roldán, Fiorella L.</creatorcontrib><creatorcontrib>Segura, Natalia</creatorcontrib><creatorcontrib>Ribal, María José</creatorcontrib><creatorcontrib>Alcaraz, Antonio</creatorcontrib><creatorcontrib>Izquierdo, Laura</creatorcontrib><creatorcontrib>Mengual, Lourdes</creatorcontrib><title>Prognostic implication of TERT promoter mutation and circulating tumor cells in muscle-invasive bladder cancer</title><title>World journal of urology</title><addtitle>World J Urol</addtitle><description>Purpose
Current clinical prognostic factors are not accurate enough to identify and monitor those muscle-invasive bladder cancer (MIBC) patients at high risk of progression after radical cystectomy (RC). Here, we determined genetic alterations in the tumor and circulating tumor cell (CTC) enumeration to find biomarkers useful for the management of MIBC after RC.
Methods
Thirty-nine MIBC patients undergoing RC were included. Tumoral tissue DNA was analyzed by next generation sequencing. CTCs were isolated from blood collected before RC and one, four and 12 months later.
Results
Sixteen (41%) patients progressed in a median time of 8.5 months and 11 (69%) of these patients harbored the
TERT
c.-124C > T mutation. All progressive patients harboring the
TERT
c.-124C > T mutation presented a significant increase in CTC number 12 months after RC compared to those without the mutation. Additionally, CTC number at 12 months was identified as an independent prognostic biomarker for tumor progression and cancer specific survival (CSS). Ten (63%) progressive patients showed an increment of CTC number with a median anticipation period of four months compared with imaging techniques.
Conclusions
The
TERT
c.-124C > T mutation could be considered a biomarker of aggressivity. CTC enumeration is a useful tool for identifying MIBC patients at high risk of progression and CSS after RC and for detecting tumor progression earlier than imaging techniques.</description><subject>Biomarkers</subject><subject>Bladder cancer</subject><subject>Cancer</subject><subject>Enumeration</subject><subject>Invasiveness</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mutation</subject><subject>Nephrology</subject><subject>Next-generation sequencing</subject><subject>Oncology</subject><subject>Original</subject><subject>Original Article</subject><subject>Patients</subject><subject>Tumor cells</subject><subject>Urology</subject><issn>1433-8726</issn><issn>0724-4983</issn><issn>1433-8726</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kUuLFTEQhYMozjj6B1wF3LhpraTSSe5GkGF8wIAi13VI0ulrhu7kmnRfmH9vxh58LVxVFfWdQxWHkOcMXjEA9boCoOg74LwDAZJ1uwfknAnETisuH_7Rn5Entd4AMCWhf0zOsFcMpZbnJH0u-ZByXaKncT5O0dsl5kTzSPdXX_b0WPKcl1DovC7bxqaB-lj8OrU5HeiyzrlQH6ap0pgaV_0UuphOtsZToG6yw9D03iYfylPyaLRTDc_u6wX5-u5qf_mhu_70_uPl2-vO91IuHQbsYbRWo1dOMLFz1jrNBPejHWHwI0N0QrCeOxesR-44Oi5HrYIegEm8IG823-Pq5jD4kJZiJ3Mscbbl1mQbzd-bFL-ZQz6ZHQfkEprBy3uDkr-voS5mjvXuSZtCXqvhUmnBueqxoS_-QW_yWlJ7r1FaK6mRqUbxjfIl11rC-OsYBuYuTrPFaVqc5mecZtdEuIlqg9MhlN_W_1H9AChmo_k</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Carrasco, Raquel</creator><creator>Ingelmo-Torres, Mercedes</creator><creator>Gómez, Ascensión</creator><creator>Roldán, Fiorella L.</creator><creator>Segura, Natalia</creator><creator>Ribal, María José</creator><creator>Alcaraz, Antonio</creator><creator>Izquierdo, Laura</creator><creator>Mengual, Lourdes</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6015-2987</orcidid></search><sort><creationdate>20220801</creationdate><title>Prognostic implication of TERT promoter mutation and circulating tumor cells in muscle-invasive bladder cancer</title><author>Carrasco, Raquel ; Ingelmo-Torres, Mercedes ; Gómez, Ascensión ; Roldán, Fiorella L. ; Segura, Natalia ; Ribal, María José ; Alcaraz, Antonio ; Izquierdo, Laura ; Mengual, Lourdes</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c566t-3e350faa83c7b4149baab8142cfaf0dcf133b44152bbeac32b23b26f87e8d0163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biomarkers</topic><topic>Bladder cancer</topic><topic>Cancer</topic><topic>Enumeration</topic><topic>Invasiveness</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mutation</topic><topic>Nephrology</topic><topic>Next-generation sequencing</topic><topic>Oncology</topic><topic>Original</topic><topic>Original Article</topic><topic>Patients</topic><topic>Tumor cells</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carrasco, Raquel</creatorcontrib><creatorcontrib>Ingelmo-Torres, Mercedes</creatorcontrib><creatorcontrib>Gómez, Ascensión</creatorcontrib><creatorcontrib>Roldán, Fiorella L.</creatorcontrib><creatorcontrib>Segura, Natalia</creatorcontrib><creatorcontrib>Ribal, María José</creatorcontrib><creatorcontrib>Alcaraz, Antonio</creatorcontrib><creatorcontrib>Izquierdo, Laura</creatorcontrib><creatorcontrib>Mengual, Lourdes</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carrasco, Raquel</au><au>Ingelmo-Torres, Mercedes</au><au>Gómez, Ascensión</au><au>Roldán, Fiorella L.</au><au>Segura, Natalia</au><au>Ribal, María José</au><au>Alcaraz, Antonio</au><au>Izquierdo, Laura</au><au>Mengual, Lourdes</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic implication of TERT promoter mutation and circulating tumor cells in muscle-invasive bladder cancer</atitle><jtitle>World journal of urology</jtitle><stitle>World J Urol</stitle><date>2022-08-01</date><risdate>2022</risdate><volume>40</volume><issue>8</issue><spage>2033</spage><epage>2039</epage><pages>2033-2039</pages><issn>1433-8726</issn><issn>0724-4983</issn><eissn>1433-8726</eissn><abstract>Purpose
Current clinical prognostic factors are not accurate enough to identify and monitor those muscle-invasive bladder cancer (MIBC) patients at high risk of progression after radical cystectomy (RC). Here, we determined genetic alterations in the tumor and circulating tumor cell (CTC) enumeration to find biomarkers useful for the management of MIBC after RC.
Methods
Thirty-nine MIBC patients undergoing RC were included. Tumoral tissue DNA was analyzed by next generation sequencing. CTCs were isolated from blood collected before RC and one, four and 12 months later.
Results
Sixteen (41%) patients progressed in a median time of 8.5 months and 11 (69%) of these patients harbored the
TERT
c.-124C > T mutation. All progressive patients harboring the
TERT
c.-124C > T mutation presented a significant increase in CTC number 12 months after RC compared to those without the mutation. Additionally, CTC number at 12 months was identified as an independent prognostic biomarker for tumor progression and cancer specific survival (CSS). Ten (63%) progressive patients showed an increment of CTC number with a median anticipation period of four months compared with imaging techniques.
Conclusions
The
TERT
c.-124C > T mutation could be considered a biomarker of aggressivity. CTC enumeration is a useful tool for identifying MIBC patients at high risk of progression and CSS after RC and for detecting tumor progression earlier than imaging techniques.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35713686</pmid><doi>10.1007/s00345-022-04061-9</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6015-2987</orcidid><oa>free_for_read</oa></addata></record> |
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source | SpringerLink Journals |
subjects | Biomarkers Bladder cancer Cancer Enumeration Invasiveness Medical prognosis Medicine Medicine & Public Health Mutation Nephrology Next-generation sequencing Oncology Original Original Article Patients Tumor cells Urology |
title | Prognostic implication of TERT promoter mutation and circulating tumor cells in muscle-invasive bladder cancer |
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