Improved cancer specific‐survival in patients with carcinoma invading bladder muscle expressing cyclo‐oxygenase‐2
Study Type – Prognosis (case series) Level of Evidence 4 OBJECTIVE To determine whether the expression of cyclo‐oxygenase (COX)‐2 has an influence on survival and on the response to chemotherapy in invasive bladder cancer. PATIENTS AND METHODS A population of 266 patients from a tertiary university...
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creator | Aziz, Anis Lessard, Annie Moore, Katherine Hovington, Hélène Latulippe, Eva Larue, Hélène Fradet, Yves Lacombe, Louis |
description | Study Type – Prognosis (case series)
Level of Evidence 4
OBJECTIVE
To determine whether the expression of cyclo‐oxygenase (COX)‐2 has an influence on survival and on the response to chemotherapy in invasive bladder cancer.
PATIENTS AND METHODS
A population of 266 patients from a tertiary university centre with carcinoma invading bladder muscle without evidence of metastasis at time of cystectomy was analyzed retrospectively. COX‐2 expression was evaluated immunohistochemically with a monoclonal anti‐COX‐2 antibody. All pertinent clinical and pathological parameters were reviewed and correlated with risk factors influencing outcome, including disease‐specific and overall survival, as well as COX‐2 expression. Immunoreactivity was categorized as positive if COX‐2 staining was present in >5% tumour cells.
RESULTS
The expression of COX‐2 was not influenced by tumour stage, grade or nodal status, nor any other parameters. The risk factors that influenced disease‐specific survival in carcinoma invading bladder muscle on multivariate analysis were lymph node status (hazards ratio, HR = 2.46 for N1, P= 0.001, HR = 2.90 for N2, P < 0.001, HR = 5.19 for N3, P= 0.012), use of neoadjuvant chemotherapy (HR = 3.54; P= 0.004) or adjuvant chemotherapy (HR = 0.57, P= 0.014) and COX‐2 expression (HR = 0.64 if >5% cells had positive expression; P= 0.025). Kaplan–Meier analysis showed an increased disease‐specific survival (P= 0.0063), as well as longer recurrence‐free survival (P= 0.003), in patients with muscle‐invasive bladder tumours expressing COX‐2 in >5% of the cells. A tendency was also observed in a subgroup with positive nodes treated with adjuvant chemotherapy (P= 0.093).
CONCLUSIONS
The overexpression of COX‐2 is associated with a better recurrence‐free and disease‐specific survival in a large cohort of 266 patients with carcinoma invading bladder muscle treated by cystectomy. A trend for increased disease‐specific survival was also observed for patients with COX‐2 overexpression and positive nodes who received adjuvant chemotherapy. Potential of COX‐2 as a prognostic marker in bladder cancer should be considered. |
doi_str_mv | 10.1111/j.1464-410X.2010.09909.x |
format | Article |
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Level of Evidence 4
OBJECTIVE
To determine whether the expression of cyclo‐oxygenase (COX)‐2 has an influence on survival and on the response to chemotherapy in invasive bladder cancer.
PATIENTS AND METHODS
A population of 266 patients from a tertiary university centre with carcinoma invading bladder muscle without evidence of metastasis at time of cystectomy was analyzed retrospectively. COX‐2 expression was evaluated immunohistochemically with a monoclonal anti‐COX‐2 antibody. All pertinent clinical and pathological parameters were reviewed and correlated with risk factors influencing outcome, including disease‐specific and overall survival, as well as COX‐2 expression. Immunoreactivity was categorized as positive if COX‐2 staining was present in >5% tumour cells.
RESULTS
The expression of COX‐2 was not influenced by tumour stage, grade or nodal status, nor any other parameters. The risk factors that influenced disease‐specific survival in carcinoma invading bladder muscle on multivariate analysis were lymph node status (hazards ratio, HR = 2.46 for N1, P= 0.001, HR = 2.90 for N2, P < 0.001, HR = 5.19 for N3, P= 0.012), use of neoadjuvant chemotherapy (HR = 3.54; P= 0.004) or adjuvant chemotherapy (HR = 0.57, P= 0.014) and COX‐2 expression (HR = 0.64 if >5% cells had positive expression; P= 0.025). Kaplan–Meier analysis showed an increased disease‐specific survival (P= 0.0063), as well as longer recurrence‐free survival (P= 0.003), in patients with muscle‐invasive bladder tumours expressing COX‐2 in >5% of the cells. A tendency was also observed in a subgroup with positive nodes treated with adjuvant chemotherapy (P= 0.093).
CONCLUSIONS
The overexpression of COX‐2 is associated with a better recurrence‐free and disease‐specific survival in a large cohort of 266 patients with carcinoma invading bladder muscle treated by cystectomy. A trend for increased disease‐specific survival was also observed for patients with COX‐2 overexpression and positive nodes who received adjuvant chemotherapy. Potential of COX‐2 as a prognostic marker in bladder cancer should be considered.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/j.1464-410X.2010.09909.x</identifier><identifier>PMID: 21166751</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Biomarkers, Tumor - metabolism ; bladder cancer ; carcinoma invading bladder muscle ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - enzymology ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Transitional Cell - drug therapy ; Carcinoma, Transitional Cell - enzymology ; Carcinoma, Transitional Cell - mortality ; Carcinoma, Transitional Cell - pathology ; COX‐2 expression ; Cyclooxygenase 2 - metabolism ; disease outcome ; Female ; Humans ; Kaplan-Meier Estimate ; Male ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness ; Nephrology. Urinary tract diseases ; Retrospective Studies ; Risk Factors ; Tumors of the urinary system ; Urinary Bladder Neoplasms - drug therapy ; Urinary Bladder Neoplasms - enzymology ; Urinary Bladder Neoplasms - mortality ; Urinary Bladder Neoplasms - pathology ; Urinary system involvement in other diseases. Miscellaneous ; Urinary tract. Prostate gland</subject><ispartof>BJU international, 2011-08, Vol.108 (4), p.531-537</ispartof><rights>2010 THE AUTHORS; BJU INTERNATIONAL © 2010 BJU INTERNATIONAL</rights><rights>2015 INIST-CNRS</rights><rights>2010 THE AUTHORS; BJU INTERNATIONAL © 2010 BJU INTERNATIONAL.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3989-e4c43c36000f8b1872064e082ef45b3d61ffb69f30887865df996ee3f2890fc03</citedby><cites>FETCH-LOGICAL-c3989-e4c43c36000f8b1872064e082ef45b3d61ffb69f30887865df996ee3f2890fc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1464-410X.2010.09909.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1464-410X.2010.09909.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24411296$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21166751$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aziz, Anis</creatorcontrib><creatorcontrib>Lessard, Annie</creatorcontrib><creatorcontrib>Moore, Katherine</creatorcontrib><creatorcontrib>Hovington, Hélène</creatorcontrib><creatorcontrib>Latulippe, Eva</creatorcontrib><creatorcontrib>Larue, Hélène</creatorcontrib><creatorcontrib>Fradet, Yves</creatorcontrib><creatorcontrib>Lacombe, Louis</creatorcontrib><title>Improved cancer specific‐survival in patients with carcinoma invading bladder muscle expressing cyclo‐oxygenase‐2</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Study Type – Prognosis (case series)
Level of Evidence 4
OBJECTIVE
To determine whether the expression of cyclo‐oxygenase (COX)‐2 has an influence on survival and on the response to chemotherapy in invasive bladder cancer.
PATIENTS AND METHODS
A population of 266 patients from a tertiary university centre with carcinoma invading bladder muscle without evidence of metastasis at time of cystectomy was analyzed retrospectively. COX‐2 expression was evaluated immunohistochemically with a monoclonal anti‐COX‐2 antibody. All pertinent clinical and pathological parameters were reviewed and correlated with risk factors influencing outcome, including disease‐specific and overall survival, as well as COX‐2 expression. Immunoreactivity was categorized as positive if COX‐2 staining was present in >5% tumour cells.
RESULTS
The expression of COX‐2 was not influenced by tumour stage, grade or nodal status, nor any other parameters. The risk factors that influenced disease‐specific survival in carcinoma invading bladder muscle on multivariate analysis were lymph node status (hazards ratio, HR = 2.46 for N1, P= 0.001, HR = 2.90 for N2, P < 0.001, HR = 5.19 for N3, P= 0.012), use of neoadjuvant chemotherapy (HR = 3.54; P= 0.004) or adjuvant chemotherapy (HR = 0.57, P= 0.014) and COX‐2 expression (HR = 0.64 if >5% cells had positive expression; P= 0.025). Kaplan–Meier analysis showed an increased disease‐specific survival (P= 0.0063), as well as longer recurrence‐free survival (P= 0.003), in patients with muscle‐invasive bladder tumours expressing COX‐2 in >5% of the cells. A tendency was also observed in a subgroup with positive nodes treated with adjuvant chemotherapy (P= 0.093).
CONCLUSIONS
The overexpression of COX‐2 is associated with a better recurrence‐free and disease‐specific survival in a large cohort of 266 patients with carcinoma invading bladder muscle treated by cystectomy. A trend for increased disease‐specific survival was also observed for patients with COX‐2 overexpression and positive nodes who received adjuvant chemotherapy. Potential of COX‐2 as a prognostic marker in bladder cancer should be considered.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>bladder cancer</subject><subject>carcinoma invading bladder muscle</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - enzymology</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Transitional Cell - drug therapy</subject><subject>Carcinoma, Transitional Cell - enzymology</subject><subject>Carcinoma, Transitional Cell - mortality</subject><subject>Carcinoma, Transitional Cell - pathology</subject><subject>COX‐2 expression</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>disease outcome</subject><subject>Female</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Tumors of the urinary system</subject><subject>Urinary Bladder Neoplasms - drug therapy</subject><subject>Urinary Bladder Neoplasms - enzymology</subject><subject>Urinary Bladder Neoplasms - mortality</subject><subject>Urinary Bladder Neoplasms - pathology</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Urinary tract. Prostate gland</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkL1uFDEQgC1ERELgFdA2iOqO8a7PZxcUEAVIFClNItFZXu84-OT9wXN7Px2PwDPyJHi5S2hx49HMNzP2x1jBYc7zeb-acyHFTHD4Ni8hZ0Fr0PPdM3b2VHj-GIOWp-wl0QogJ-TiBTstOZdyueBnbHvVDqnfYFM42zlMBQ3ogg_u989fNKZN2NhYhK4Y7Dpgt6ZiG9bfM5tc6PrW5tLGNqF7KOpomyb3tyO5iAXuhoREU8XtXezzuH63f8DOEua4fMVOvI2Er4_3Obv_fHl38XV2c_vl6uLjzcxVWukZCicqV0kA8KrmalmCFAiqRC8WddVI7n0tta9AqaWSi8ZrLRErXyoN3kF1zt4d5uZf_hiR1qYN5DBG22E_klEK-DR-mUl1IF3qiRJ6M6TQ2rQ3HMxk3azMJNRMcs1k3fy1bna59c1xyVi32Dw1PmrOwNsjYMnZ6FN2HegfJwTnpZaZ-3DgtiHi_r8fYD5d309R9QdoSqLG</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Aziz, Anis</creator><creator>Lessard, Annie</creator><creator>Moore, Katherine</creator><creator>Hovington, Hélène</creator><creator>Latulippe, Eva</creator><creator>Larue, Hélène</creator><creator>Fradet, Yves</creator><creator>Lacombe, Louis</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</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>201108</creationdate><title>Improved cancer specific‐survival in patients with carcinoma invading bladder muscle expressing cyclo‐oxygenase‐2</title><author>Aziz, Anis ; Lessard, Annie ; Moore, Katherine ; Hovington, Hélène ; Latulippe, Eva ; Larue, Hélène ; Fradet, Yves ; Lacombe, Louis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3989-e4c43c36000f8b1872064e082ef45b3d61ffb69f30887865df996ee3f2890fc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>bladder cancer</topic><topic>carcinoma invading bladder muscle</topic><topic>Carcinoma, Squamous Cell - drug therapy</topic><topic>Carcinoma, Squamous Cell - enzymology</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Transitional Cell - drug therapy</topic><topic>Carcinoma, Transitional Cell - enzymology</topic><topic>Carcinoma, Transitional Cell - mortality</topic><topic>Carcinoma, Transitional Cell - pathology</topic><topic>COX‐2 expression</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>disease outcome</topic><topic>Female</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Tumors of the urinary system</topic><topic>Urinary Bladder Neoplasms - drug therapy</topic><topic>Urinary Bladder Neoplasms - enzymology</topic><topic>Urinary Bladder Neoplasms - mortality</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aziz, Anis</creatorcontrib><creatorcontrib>Lessard, Annie</creatorcontrib><creatorcontrib>Moore, Katherine</creatorcontrib><creatorcontrib>Hovington, Hélène</creatorcontrib><creatorcontrib>Latulippe, Eva</creatorcontrib><creatorcontrib>Larue, Hélène</creatorcontrib><creatorcontrib>Fradet, Yves</creatorcontrib><creatorcontrib>Lacombe, Louis</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>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aziz, Anis</au><au>Lessard, Annie</au><au>Moore, Katherine</au><au>Hovington, Hélène</au><au>Latulippe, Eva</au><au>Larue, Hélène</au><au>Fradet, Yves</au><au>Lacombe, Louis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved cancer specific‐survival in patients with carcinoma invading bladder muscle expressing cyclo‐oxygenase‐2</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2011-08</date><risdate>2011</risdate><volume>108</volume><issue>4</issue><spage>531</spage><epage>537</epage><pages>531-537</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>Study Type – Prognosis (case series)
Level of Evidence 4
OBJECTIVE
To determine whether the expression of cyclo‐oxygenase (COX)‐2 has an influence on survival and on the response to chemotherapy in invasive bladder cancer.
PATIENTS AND METHODS
A population of 266 patients from a tertiary university centre with carcinoma invading bladder muscle without evidence of metastasis at time of cystectomy was analyzed retrospectively. COX‐2 expression was evaluated immunohistochemically with a monoclonal anti‐COX‐2 antibody. All pertinent clinical and pathological parameters were reviewed and correlated with risk factors influencing outcome, including disease‐specific and overall survival, as well as COX‐2 expression. Immunoreactivity was categorized as positive if COX‐2 staining was present in >5% tumour cells.
RESULTS
The expression of COX‐2 was not influenced by tumour stage, grade or nodal status, nor any other parameters. The risk factors that influenced disease‐specific survival in carcinoma invading bladder muscle on multivariate analysis were lymph node status (hazards ratio, HR = 2.46 for N1, P= 0.001, HR = 2.90 for N2, P < 0.001, HR = 5.19 for N3, P= 0.012), use of neoadjuvant chemotherapy (HR = 3.54; P= 0.004) or adjuvant chemotherapy (HR = 0.57, P= 0.014) and COX‐2 expression (HR = 0.64 if >5% cells had positive expression; P= 0.025). Kaplan–Meier analysis showed an increased disease‐specific survival (P= 0.0063), as well as longer recurrence‐free survival (P= 0.003), in patients with muscle‐invasive bladder tumours expressing COX‐2 in >5% of the cells. A tendency was also observed in a subgroup with positive nodes treated with adjuvant chemotherapy (P= 0.093).
CONCLUSIONS
The overexpression of COX‐2 is associated with a better recurrence‐free and disease‐specific survival in a large cohort of 266 patients with carcinoma invading bladder muscle treated by cystectomy. A trend for increased disease‐specific survival was also observed for patients with COX‐2 overexpression and positive nodes who received adjuvant chemotherapy. Potential of COX‐2 as a prognostic marker in bladder cancer should be considered.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21166751</pmid><doi>10.1111/j.1464-410X.2010.09909.x</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic Agents - therapeutic use Biological and medical sciences Biomarkers, Tumor - metabolism bladder cancer carcinoma invading bladder muscle Carcinoma, Squamous Cell - drug therapy Carcinoma, Squamous Cell - enzymology Carcinoma, Squamous Cell - mortality Carcinoma, Squamous Cell - pathology Carcinoma, Transitional Cell - drug therapy Carcinoma, Transitional Cell - enzymology Carcinoma, Transitional Cell - mortality Carcinoma, Transitional Cell - pathology COX‐2 expression Cyclooxygenase 2 - metabolism disease outcome Female Humans Kaplan-Meier Estimate Male Medical sciences Middle Aged Neoplasm Invasiveness Nephrology. Urinary tract diseases Retrospective Studies Risk Factors Tumors of the urinary system Urinary Bladder Neoplasms - drug therapy Urinary Bladder Neoplasms - enzymology Urinary Bladder Neoplasms - mortality Urinary Bladder Neoplasms - pathology Urinary system involvement in other diseases. Miscellaneous Urinary tract. Prostate gland |
title | Improved cancer specific‐survival in patients with carcinoma invading bladder muscle expressing cyclo‐oxygenase‐2 |
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