Improved cancer specific-survival in patients with carcinoma invading bladder muscle expressing cyclo-oxygenase-2

被引:9
作者
Aziz, Anis [1 ]
Lessard, Annie [2 ]
Moore, Katherine [2 ]
Hovington, Helene [2 ]
Latulippe, Eva [3 ]
Larue, Helene [2 ]
Fradet, Yves [1 ,2 ]
Lacombe, Louis [1 ,2 ]
机构
[1] Hop Hotel Dieu, CHUQ, Dept Surg, Serv Urol, Quebec City, PQ G1R 2J6, Canada
[2] Hop Hotel Dieu, CHUQ, Lab Urooncol Expt, Quebec City, PQ G1R 2J6, Canada
[3] Hop Hotel Dieu, CHUQ, Dept Pathol, Quebec City, PQ G1R 2J6, Canada
关键词
bladder cancer; COX-2; expression; disease outcome; carcinoma invading bladder muscle; TRANSITIONAL-CELL CARCINOMA; URINARY-BLADDER; PHASE-II; CYCLOOXYGENASE-2; EXPRESSION; MOLECULAR PATHOLOGY; TUMOR RESPONSE; CANINE MODEL; LUNG-CANCER; IN-VITRO; CELECOXIB;
D O I
10.1111/j.1464-410X.2010.09909.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:531 / 537
页数:7
相关论文
共 32 条
[1]   Gefitinib plus celecoxilb in chernotherapy-naive patients with stage IIIB/IV non-small cell lung cancer - A phase II study from the Hoosier Oncology Group [J].
Agarwala, Anuj ;
Fisher, William ;
Bruetman, Daniel ;
McClean, John ;
Taber, David ;
Titzer, Michael ;
Juliar, Beth ;
Yu, Menggang ;
Breen, Tim ;
Einhorn, Lawrence H. ;
Hanna, Nasser .
JOURNAL OF THORACIC ONCOLOGY, 2008, 3 (04) :374-379
[2]   COX-2 and NF-KB overexpression is common in pancreatic cancer but does not predict for COX-2 inhibitors activity in combination with gemcitabine and oxaliplatin [J].
Cascinu, Stefano ;
Scartozzi, Mario ;
Carbonari, Giovanna ;
Pierantoni, Chiara ;
Verdecchia, Lorena ;
Mariani, Cinzia ;
Squadroni, Michela ;
Antognoli, Stefania ;
Silva, Rosa Rita ;
Giampieri, Riccardo ;
Berardi, Rossana .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2007, 30 (05) :526-530
[3]  
Castelao JE, 2000, BRIT J CANCER, V82, P1364
[4]   Cyclooxygenase-2 dependent and independent antitumor effects induced by celecoxib in urinary bladder cancer cells [J].
Dhawan, Deepika ;
Jeffreys, Antonella Borgatti ;
Zheng, Rong ;
Stewart, Jane C. ;
Knapp, Deborah W. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (04) :897-904
[5]   Gemcitabine plus celecoxib in patients with advanced or metastatic pancreatic adenocarcinoma - Results of a phase II trial [J].
Dragovich, Tomislav ;
Burris, Howard, III ;
Loehrer, Patrick ;
Von Hoff, Daniel D. ;
Chow, Sherry ;
Stratton, Steven ;
Green, Sylvan ;
Obregon, Yrma ;
Alvarez, Irene ;
Gordon, Michael .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2008, 31 (02) :157-162
[6]   Impact of celecoxib on capecitabine tolerability and activity in pretreated metastatic breast cancer: results of a phase II study with biomarker evaluation [J].
Fabi, Alessandra ;
Metro, Giulio ;
Papaldo, Paola ;
Mottolese, Marcella ;
Melucci, Elisa ;
Carlini, Paolo ;
Sperduti, Isabella ;
Russillo, Michelangelo ;
Gelibter, Alain ;
Ferretti, Gianluigi ;
Tomao, Silverio ;
Milella, Michele ;
Cognetti, Francesco .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2008, 62 (04) :717-725
[7]  
Fosslien E, 2000, ANN CLIN LAB SCI, V30, P3
[8]  
Fosslien E, 2001, ANN CLIN LAB SCI, V31, P325
[9]   A phase II study of acute toxicity for celebrex™ (celecoxib) and chemoradiation in patients with locally advanced cervical cancer:: Primary endpoint analysis of RTOG 0128 [J].
Gaffney, David K. ;
Winter, Kathryn ;
Dicker, Adam P. ;
Miller, Brigitte ;
Eifel, Patricia J. ;
Ryu, Janice ;
Avizonis, Vilija ;
Fromm, Mitch ;
Greven, Kathryn .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 67 (01) :104-109
[10]   Chemopreventive effects of cyclooxygenase-2 inhibitor and epidermal growth factor-receptor kinase inhibitor on rat urinary bladder carcinogenesis [J].
Hattori, K ;
Iida, K ;
Joraku, A ;
Tsukamoto, S ;
Akaza, H ;
Oyasu, R .
BJU INTERNATIONAL, 2006, 97 (03) :640-643