Comparative Outcomes of Primary, Recurrent, and Progressive High-risk Non–muscle-invasive Bladder Cancer
Abstract Background The treatment of high-risk non–muscle-invasive bladder cancer (BCa) is problematic given the variable natural history of the disease. Few reports have compared outcomes for primary high-risk tumours with those that develop following previous BCas (relapses). The latter represent...
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description | Abstract Background The treatment of high-risk non–muscle-invasive bladder cancer (BCa) is problematic given the variable natural history of the disease. Few reports have compared outcomes for primary high-risk tumours with those that develop following previous BCas (relapses). The latter represent a self-selected cohort, having failed previous treatments. Objective To compare outcomes in patients with primary, progressive, and recurrent high-risk non–muscle-invasive BCa. Design, setting, and participants We identified all patients with primary and relapsing high-risk BCa tumours at our institution since 1994. Relapses were divided into progressive (previous low- or intermediate-risk disease) and recurrent (previous high-risk disease) cancers. Outcome measurements and statistical analysis Relationships with outcome analysed using multivariable Cox regression and log-rank analysis. Results and limitations We identified 699 primary, 110 progressive, and 494 recurrent high-risk BCa tumours in 809 patients (average follow-up: 59 mo [interquartile range: 6–190]). Muscle invasion occurred most commonly in recurrent (23%) tumours, when compared to progressive (20%) and primary (14.6%) cohorts (log rank p < 0.001). Disease-specific mortality (DSM) occurred more frequently in patients with recurrent (25.5%) and progressive (24.6%) tumours compared to primary disease (19.2%; log rank p = 0.006). Other-cause mortality was similar in all groups (log rank p = 0.57), and overall mortality was highest in the progressive cohort (62%) compared with the recurrent (58%) and primary groups (54%; log rank p < 0.001). In multivariable analysis, progression and DSM were predicted by tumour grouping (hazard ratio [HR]: >1.15; p < 0.026), stage (HR: >1.30; p < 0.001), and patient age and sex (HR: >1.03; p < 0.037). Carcinoma in situ was only predictive of outcome in primary tumors. Limitations include retrospective design and limited details regarding bacillus Camille-Guérin use. Conclusions Patients with relapsing, high-risk, BCa tumors have higher progression, DSM, and overall mortality rates than those with primary cancers. The use of bladder-sparing strategies in these patients should approached cautiously. Carcinoma in situ has little predicative role in relapsing, high-risk, BCa tumors. |
doi_str_mv | 10.1016/j.eururo.2012.08.064 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1237506109</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0302283812010172</els_id><sourcerecordid>1237506109</sourcerecordid><originalsourceid>FETCH-LOGICAL-c513t-fa8869df2c03b4f56e34ca490f829dfcd409dfe006416ee08cb71259947bc7863</originalsourceid><addsrcrecordid>eNqFks1u1DAQgC0EokvhDRDKBYlDE8Z2YjsXJFgBRaoo4udseZ1JcZrEWztZqTfegTfkSXDIAhIXTiONv5nxfBpCHlMoKFDxvCtwDnPwBQPKClAFiPIO2VAleS4rAXfJBjiwnCmuTsiDGDsA4FXN75MTxmpVyVJsSLf1w94EM7kDZpfzZP2AMfNt9iG4wYTbs-wj2jkEHKezzIxNyvurgDEu_Lm7-poHF6-z93788e37MEfbY-7Gg_n1_qo3TYMh25rRYnhI7rWmj_joGE_JlzevP2_P84vLt--2Ly9yW1E-5a1RStRNyyzwXdlWAnlpTVlDq1hK26aEFBDSulQggrI7SVlV16XcWakEPyXP1r774G9mjJMeXLTY92ZEP0dNGZcVCAp1QssVtcHHGLDV-3VtTUEvlnWnV8t6saxB6TQ2lT05Tph3AzZ_in5rTcDTI2CiNX0bkgAX_3JCclrVC_di5TD5ODgMOlqHSVbjAtpJN9797yf_NrC9G12aeY23GDs_hzG51lTHVKM_LRexHARNTYBKxn8CFXmzfg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1237506109</pqid></control><display><type>article</type><title>Comparative Outcomes of Primary, Recurrent, and Progressive High-risk Non–muscle-invasive Bladder Cancer</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Thomas, Francis ; Noon, Aidan P ; Rubin, Naomi ; Goepel, John R ; Catto, James W.F</creator><creatorcontrib>Thomas, Francis ; Noon, Aidan P ; Rubin, Naomi ; Goepel, John R ; Catto, James W.F</creatorcontrib><description>Abstract Background The treatment of high-risk non–muscle-invasive bladder cancer (BCa) is problematic given the variable natural history of the disease. Few reports have compared outcomes for primary high-risk tumours with those that develop following previous BCas (relapses). The latter represent a self-selected cohort, having failed previous treatments. Objective To compare outcomes in patients with primary, progressive, and recurrent high-risk non–muscle-invasive BCa. Design, setting, and participants We identified all patients with primary and relapsing high-risk BCa tumours at our institution since 1994. Relapses were divided into progressive (previous low- or intermediate-risk disease) and recurrent (previous high-risk disease) cancers. Outcome measurements and statistical analysis Relationships with outcome analysed using multivariable Cox regression and log-rank analysis. Results and limitations We identified 699 primary, 110 progressive, and 494 recurrent high-risk BCa tumours in 809 patients (average follow-up: 59 mo [interquartile range: 6–190]). Muscle invasion occurred most commonly in recurrent (23%) tumours, when compared to progressive (20%) and primary (14.6%) cohorts (log rank p < 0.001). Disease-specific mortality (DSM) occurred more frequently in patients with recurrent (25.5%) and progressive (24.6%) tumours compared to primary disease (19.2%; log rank p = 0.006). Other-cause mortality was similar in all groups (log rank p = 0.57), and overall mortality was highest in the progressive cohort (62%) compared with the recurrent (58%) and primary groups (54%; log rank p < 0.001). In multivariable analysis, progression and DSM were predicted by tumour grouping (hazard ratio [HR]: >1.15; p < 0.026), stage (HR: >1.30; p < 0.001), and patient age and sex (HR: >1.03; p < 0.037). Carcinoma in situ was only predictive of outcome in primary tumors. Limitations include retrospective design and limited details regarding bacillus Camille-Guérin use. Conclusions Patients with relapsing, high-risk, BCa tumors have higher progression, DSM, and overall mortality rates than those with primary cancers. The use of bladder-sparing strategies in these patients should approached cautiously. Carcinoma in situ has little predicative role in relapsing, high-risk, BCa tumors.</description><identifier>ISSN: 0302-2838</identifier><identifier>EISSN: 1873-7560</identifier><identifier>DOI: 10.1016/j.eururo.2012.08.064</identifier><identifier>PMID: 22985746</identifier><identifier>CODEN: EUURAV</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Administration, Intravesical ; Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents - administration & dosage ; BCG Vaccine - administration & dosage ; Biological and medical sciences ; Bladder cancer ; Carcinoma - mortality ; Carcinoma - pathology ; Carcinoma - therapy ; Carcinoma in Situ - mortality ; Carcinoma in Situ - pathology ; Carcinoma in Situ - therapy ; CIS ; Disease Progression ; Disease-Free Survival ; England - epidemiology ; Female ; High-risk ; Humans ; Kaplan-Meier Estimate ; Male ; Medical sciences ; Middle Aged ; Multivariate Analysis ; Neoplasm Invasiveness ; Neoplasm Recurrence, Local - mortality ; Neoplasm Recurrence, Local - pathology ; Neoplasm Recurrence, Local - therapy ; Nephrology. Urinary tract diseases ; Outcome ; Prognosis ; Proportional Hazards Models ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Time Factors ; Treatment Outcome ; Tumors of the urinary system ; Urinary Bladder Neoplasms - mortality ; Urinary Bladder Neoplasms - pathology ; Urinary Bladder Neoplasms - therapy ; Urinary system involvement in other diseases. Miscellaneous ; Urinary tract. Prostate gland ; Urology</subject><ispartof>European urology, 2013-01, Vol.63 (1), p.145-154</ispartof><rights>2012</rights><rights>2014 INIST-CNRS</rights><rights>Crown Copyright © 2012. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-fa8869df2c03b4f56e34ca490f829dfcd409dfe006416ee08cb71259947bc7863</citedby><cites>FETCH-LOGICAL-c513t-fa8869df2c03b4f56e34ca490f829dfcd409dfe006416ee08cb71259947bc7863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.eururo.2012.08.064$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26731596$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22985746$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thomas, Francis</creatorcontrib><creatorcontrib>Noon, Aidan P</creatorcontrib><creatorcontrib>Rubin, Naomi</creatorcontrib><creatorcontrib>Goepel, John R</creatorcontrib><creatorcontrib>Catto, James W.F</creatorcontrib><title>Comparative Outcomes of Primary, Recurrent, and Progressive High-risk Non–muscle-invasive Bladder Cancer</title><title>European urology</title><addtitle>Eur Urol</addtitle><description>Abstract Background The treatment of high-risk non–muscle-invasive bladder cancer (BCa) is problematic given the variable natural history of the disease. Few reports have compared outcomes for primary high-risk tumours with those that develop following previous BCas (relapses). The latter represent a self-selected cohort, having failed previous treatments. Objective To compare outcomes in patients with primary, progressive, and recurrent high-risk non–muscle-invasive BCa. Design, setting, and participants We identified all patients with primary and relapsing high-risk BCa tumours at our institution since 1994. Relapses were divided into progressive (previous low- or intermediate-risk disease) and recurrent (previous high-risk disease) cancers. Outcome measurements and statistical analysis Relationships with outcome analysed using multivariable Cox regression and log-rank analysis. Results and limitations We identified 699 primary, 110 progressive, and 494 recurrent high-risk BCa tumours in 809 patients (average follow-up: 59 mo [interquartile range: 6–190]). Muscle invasion occurred most commonly in recurrent (23%) tumours, when compared to progressive (20%) and primary (14.6%) cohorts (log rank p < 0.001). Disease-specific mortality (DSM) occurred more frequently in patients with recurrent (25.5%) and progressive (24.6%) tumours compared to primary disease (19.2%; log rank p = 0.006). Other-cause mortality was similar in all groups (log rank p = 0.57), and overall mortality was highest in the progressive cohort (62%) compared with the recurrent (58%) and primary groups (54%; log rank p < 0.001). In multivariable analysis, progression and DSM were predicted by tumour grouping (hazard ratio [HR]: >1.15; p < 0.026), stage (HR: >1.30; p < 0.001), and patient age and sex (HR: >1.03; p < 0.037). Carcinoma in situ was only predictive of outcome in primary tumors. Limitations include retrospective design and limited details regarding bacillus Camille-Guérin use. Conclusions Patients with relapsing, high-risk, BCa tumors have higher progression, DSM, and overall mortality rates than those with primary cancers. The use of bladder-sparing strategies in these patients should approached cautiously. Carcinoma in situ has little predicative role in relapsing, high-risk, BCa tumors.</description><subject>Administration, Intravesical</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>BCG Vaccine - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Bladder cancer</subject><subject>Carcinoma - mortality</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma - therapy</subject><subject>Carcinoma in Situ - mortality</subject><subject>Carcinoma in Situ - pathology</subject><subject>Carcinoma in Situ - therapy</subject><subject>CIS</subject><subject>Disease Progression</subject><subject>Disease-Free Survival</subject><subject>England - epidemiology</subject><subject>Female</subject><subject>High-risk</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Recurrence, Local - mortality</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Recurrence, Local - therapy</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Outcome</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Tumors of the urinary system</subject><subject>Urinary Bladder Neoplasms - mortality</subject><subject>Urinary Bladder Neoplasms - pathology</subject><subject>Urinary Bladder Neoplasms - therapy</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Urinary tract. Prostate gland</subject><subject>Urology</subject><issn>0302-2838</issn><issn>1873-7560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1u1DAQgC0EokvhDRDKBYlDE8Z2YjsXJFgBRaoo4udseZ1JcZrEWztZqTfegTfkSXDIAhIXTiONv5nxfBpCHlMoKFDxvCtwDnPwBQPKClAFiPIO2VAleS4rAXfJBjiwnCmuTsiDGDsA4FXN75MTxmpVyVJsSLf1w94EM7kDZpfzZP2AMfNt9iG4wYTbs-wj2jkEHKezzIxNyvurgDEu_Lm7-poHF6-z93788e37MEfbY-7Gg_n1_qo3TYMh25rRYnhI7rWmj_joGE_JlzevP2_P84vLt--2Ly9yW1E-5a1RStRNyyzwXdlWAnlpTVlDq1hK26aEFBDSulQggrI7SVlV16XcWakEPyXP1r774G9mjJMeXLTY92ZEP0dNGZcVCAp1QssVtcHHGLDV-3VtTUEvlnWnV8t6saxB6TQ2lT05Tph3AzZ_in5rTcDTI2CiNX0bkgAX_3JCclrVC_di5TD5ODgMOlqHSVbjAtpJN9797yf_NrC9G12aeY23GDs_hzG51lTHVKM_LRexHARNTYBKxn8CFXmzfg</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Thomas, Francis</creator><creator>Noon, Aidan P</creator><creator>Rubin, Naomi</creator><creator>Goepel, John R</creator><creator>Catto, James W.F</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130101</creationdate><title>Comparative Outcomes of Primary, Recurrent, and Progressive High-risk Non–muscle-invasive Bladder Cancer</title><author>Thomas, Francis ; Noon, Aidan P ; Rubin, Naomi ; Goepel, John R ; Catto, James W.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-fa8869df2c03b4f56e34ca490f829dfcd409dfe006416ee08cb71259947bc7863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Administration, Intravesical</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>BCG Vaccine - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Bladder cancer</topic><topic>Carcinoma - mortality</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma - therapy</topic><topic>Carcinoma in Situ - mortality</topic><topic>Carcinoma in Situ - pathology</topic><topic>Carcinoma in Situ - therapy</topic><topic>CIS</topic><topic>Disease Progression</topic><topic>Disease-Free Survival</topic><topic>England - epidemiology</topic><topic>Female</topic><topic>High-risk</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Recurrence, Local - mortality</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Recurrence, Local - therapy</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Outcome</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Tumors of the urinary system</topic><topic>Urinary Bladder Neoplasms - mortality</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Urinary Bladder Neoplasms - therapy</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Urinary tract. Prostate gland</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomas, Francis</creatorcontrib><creatorcontrib>Noon, Aidan P</creatorcontrib><creatorcontrib>Rubin, Naomi</creatorcontrib><creatorcontrib>Goepel, John R</creatorcontrib><creatorcontrib>Catto, James W.F</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomas, Francis</au><au>Noon, Aidan P</au><au>Rubin, Naomi</au><au>Goepel, John R</au><au>Catto, James W.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Outcomes of Primary, Recurrent, and Progressive High-risk Non–muscle-invasive Bladder Cancer</atitle><jtitle>European urology</jtitle><addtitle>Eur Urol</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>63</volume><issue>1</issue><spage>145</spage><epage>154</epage><pages>145-154</pages><issn>0302-2838</issn><eissn>1873-7560</eissn><coden>EUURAV</coden><abstract>Abstract Background The treatment of high-risk non–muscle-invasive bladder cancer (BCa) is problematic given the variable natural history of the disease. Few reports have compared outcomes for primary high-risk tumours with those that develop following previous BCas (relapses). The latter represent a self-selected cohort, having failed previous treatments. Objective To compare outcomes in patients with primary, progressive, and recurrent high-risk non–muscle-invasive BCa. Design, setting, and participants We identified all patients with primary and relapsing high-risk BCa tumours at our institution since 1994. Relapses were divided into progressive (previous low- or intermediate-risk disease) and recurrent (previous high-risk disease) cancers. Outcome measurements and statistical analysis Relationships with outcome analysed using multivariable Cox regression and log-rank analysis. Results and limitations We identified 699 primary, 110 progressive, and 494 recurrent high-risk BCa tumours in 809 patients (average follow-up: 59 mo [interquartile range: 6–190]). Muscle invasion occurred most commonly in recurrent (23%) tumours, when compared to progressive (20%) and primary (14.6%) cohorts (log rank p < 0.001). Disease-specific mortality (DSM) occurred more frequently in patients with recurrent (25.5%) and progressive (24.6%) tumours compared to primary disease (19.2%; log rank p = 0.006). Other-cause mortality was similar in all groups (log rank p = 0.57), and overall mortality was highest in the progressive cohort (62%) compared with the recurrent (58%) and primary groups (54%; log rank p < 0.001). In multivariable analysis, progression and DSM were predicted by tumour grouping (hazard ratio [HR]: >1.15; p < 0.026), stage (HR: >1.30; p < 0.001), and patient age and sex (HR: >1.03; p < 0.037). Carcinoma in situ was only predictive of outcome in primary tumors. Limitations include retrospective design and limited details regarding bacillus Camille-Guérin use. Conclusions Patients with relapsing, high-risk, BCa tumors have higher progression, DSM, and overall mortality rates than those with primary cancers. The use of bladder-sparing strategies in these patients should approached cautiously. Carcinoma in situ has little predicative role in relapsing, high-risk, BCa tumors.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>22985746</pmid><doi>10.1016/j.eururo.2012.08.064</doi><tpages>10</tpages></addata></record> |
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subjects | Administration, Intravesical Adult Aged Aged, 80 and over Antineoplastic Agents - administration & dosage BCG Vaccine - administration & dosage Biological and medical sciences Bladder cancer Carcinoma - mortality Carcinoma - pathology Carcinoma - therapy Carcinoma in Situ - mortality Carcinoma in Situ - pathology Carcinoma in Situ - therapy CIS Disease Progression Disease-Free Survival England - epidemiology Female High-risk Humans Kaplan-Meier Estimate Male Medical sciences Middle Aged Multivariate Analysis Neoplasm Invasiveness Neoplasm Recurrence, Local - mortality Neoplasm Recurrence, Local - pathology Neoplasm Recurrence, Local - therapy Nephrology. Urinary tract diseases Outcome Prognosis Proportional Hazards Models Retrospective Studies Risk Assessment Risk Factors Time Factors Treatment Outcome Tumors of the urinary system Urinary Bladder Neoplasms - mortality Urinary Bladder Neoplasms - pathology Urinary Bladder Neoplasms - therapy Urinary system involvement in other diseases. Miscellaneous Urinary tract. Prostate gland Urology |
title | Comparative Outcomes of Primary, Recurrent, and Progressive High-risk Non–muscle-invasive Bladder Cancer |
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