Prognostic role of the ratio between cyclooxygenase-2 in tumor and stroma compartments in cervical cancer

被引:34
作者
Ferrandina, G
Ranelletti, FO
Legge, F
Gessi, M
Salutari, V
Distefano, MG
Lauriola, L
Zannoni, GF
Martinelli, E
Scambia, G
机构
[1] Univ Cattolica Sacro Cuore, Dept Obstet & Gynecol, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Dept Histol, I-00168 Rome, Italy
[3] Univ Cattolica Sacro Cuore, Dept Pathol, I-00168 Rome, Italy
关键词
D O I
10.1158/1078-0432.CCR-1090-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of this study was to analyze the clinical role of cyclooxygenase (COX)-2 in a large series of 175 cervical cancer patients. Experimental Design: Immunohistochemistry was performed on paraffin-embedded sections by using rabbit an-tiserum against COX-2. The tumor:stroma (T/S) ratio of COX-2 expression was used to define the overall COX-2 content in the tumor. Results: The T/S COX-2 ratio values ranged from 0.03 to 48.2 (mean +/- SE, 3.7 +/- 0.5). A total of 95 of 175 patients (54.3%) were scored as having a high (>1) T/S COX-2 ratio. In locally advanced cervical cancer patients who underwent neoadjuvant treatment, the percentage of cases showing a high T/S COX-2 ratio was greater in patients who did not respond to treatment (26 of 29 patients, 89.7%) than in patients with a partial (32 of 50 patients, 64.0%) or complete (19 of 44 patients, 43.2%) response (P = 0.0003). When logistic regression was applied, International Federation of Gynecologists and Obstetricians (FIGO) stage (X-2 11.3; P = 0.0008) and T/S COX-2 ratio (X-2 = 5.3; P 0.021) retained an independent role in predicting a poor chance of response. Cases with a high T/S COX-2 ratio had a shorter overall survival (OS) [2-year OS, 61%(95% confidence interval 750-83)] than cases with a low T/S COX-2 ratio (2-year OS, 90%; 95% confidence interval, 81-99; P = 0.0001). In multivariate analysis, the status of T/S COX-2 IDV ratio, together with advanced stage, retained an independent negative prognostic role for OS. Conclusions: The assessment of COX-2 status in both tumor and stroma compartment could provide valuable information to identify cervical cancer patients endowed with a very poor chance of response to neoadjuvant treatment and unfavorable prognosis.
引用
收藏
页码:3117 / 3123
页数:7
相关论文
共 36 条
[1]   DANGERS OF USING OPTIMAL CUTPOINTS IN THE EVALUATION OF PROGNOSTIC FACTORS [J].
ALTMAN, DG ;
LAUSEN, B ;
SAUERBREI, W ;
SCHUMACHER, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (11) :829-835
[2]  
[Anonymous], 1989, Analysis of binary data
[3]  
BenedettiPanici P, 1996, CANCER-AM CANCER SOC, V78, P2359, DOI 10.1002/(SICI)1097-0142(19961201)78:11<2359::AID-CNCR14>3.0.CO
[4]  
2-#
[5]   High cyclooxygenase-2 expression in cervical adenocarcinomas [J].
Chen, YJ ;
Wang, LS ;
Wang, PH ;
Lai, CR ;
Yen, MS ;
Ng, HT ;
Yuan, CC .
GYNECOLOGIC ONCOLOGY, 2003, 88 (03) :379-385
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]   Cyclo-oxygenase 2: a pharmacological target for the prevention of cancer [J].
Dannenberg, AJ ;
Altorki, NK ;
Boyle, JO ;
Dang, C ;
Howe, LR ;
Weksler, BB ;
Subbararnaiah, K .
LANCET ONCOLOGY, 2001, 2 (09) :544-551
[8]   Cyclooxygenase-2 expression in endometrial carcinoma - Correlation with clinicopathologic parameters and clinical outcome [J].
Ferrandina, G ;
Legge, F ;
Ranelletti, FO ;
Zannoni, GF ;
Maggiano, N ;
Evangelisti, A ;
Mancuso, S ;
Scambia, G ;
Lauriola, L .
CANCER, 2002, 95 (04) :801-807
[9]   Increased cyclooxygenase-2 expression is associated with chemotherapy resistance and poor survival in cervical cancer patients [J].
Ferrandina, G ;
Lauriola, L ;
Distefano, MG ;
Zannoni, GF ;
Gessi, M ;
Legge, F ;
Maggiano, N ;
Mancuso, S ;
Capelli, A ;
Scambia, G ;
Ranelletti, FO .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (04) :973-981
[10]  
Ferrandina G, 2003, CLIN CANCER RES, V9, P4324