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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Veröffentlicht in:BJU international 2011-08, Vol.108 (4), p.531-537
Hauptverfasser: Aziz, Anis, Lessard, Annie, Moore, Katherine, Hovington, Hélène, Latulippe, Eva, Larue, Hélène, Fradet, Yves, Lacombe, Louis
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container_end_page 537
container_issue 4
container_start_page 531
container_title BJU international
container_volume 108
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
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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 &gt;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 &lt; 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 &gt;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 &gt;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. 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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 &gt;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 &lt; 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 &gt;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 &gt;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 &gt;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 &lt; 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 &gt;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 &gt;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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