Published data on the prognostic value of cyclooxygenase-2 (COX-2) overexpression in cervical cancer are conflicting and heterogeneous. We performed a meta-analysis to more precisely estimate its prognostic significance. The pooled hazard ratios (HRs) or odds ratios (ORs) with 95% confidence intervals (CIs) were used to estimate the effects. Twenty-three studies with 1,477 cervical cancer patients were selected to evaluate the association between COX-2 and overall survival (OS), disease-free survival (DFS), response to chemoradiation (RC) and clinicopathological parameters. High COX-2 expression predicted poor OS (HR: 2.53, 95% CI: 1.54-4.18), DFS (HR: 2.41, 95% CI: 1.58-3.69) and RC (OR: 3.03, 95% CI: 1.97-4.64). Subgroup analyses showed that COX-2 overexpression was related significantly with poor OS in patients treated by chemoradiation or surgery, and in patients with squamous cell carcinoma, respectively. Besides, COX-2 overexpression was related significantly with poor DFS in chemoradiation subgroup. Furthermore, COX-2 overexpression was associated with poor RC in patients who received ''FP'' regimen or ''P'' regimen. Additionally, there were significant associations between COX-2 expression and all clinicopathological parameters except tumor grade. The pooled ORs (95% CI) were as follows: 1.49 (1.09-2.04) for age, 1.77 (1.22-2.56) for lymph node metastasis, 1.04 (0.74-1.47) for tumor grade, 1.71 (1.12-2.64) for tumor size, 2.38 (1.28-4.45) for FIGO stage, 3.96 (2.32-6.77) for histological type, 2.45(1.10-5.42) for parametrical involvement. This meta-analysis indicated that COX-2 overexpression might be an unfavorable prognostic and a chemoradiation resistance predictive factor for cervical cancer; it could potentially help to stratify patients further in clinical treatment.Cervical cancer is the second most common cancer in women worldwide and is a leading cause of cancer-related death in women in developing countries. Despite the public health importance of cervical cancer, factors which influence the outcome of these patients are not completely understood. It is valuable to identify molecular predictive markers for the prognosis, which would be helpful in the selection of therapeutic strategies and further improve patient survival for cervical cancer. Multiple biomarkers with potential prognostic value have been evaluated in cervical cancer, such as epidermal growth factor receptor (EGFR), 1,2 Carbonic anhydrase IX (CAIX), 3,4 vascular endothelial growth factor (VEGF) 5,6 and Cyclooxygenase-2 (COX-2), 7,8 however, there remains some controversy. Additionally, coexpression of multiple biomarkers (such as COX-2, VEGF, EGFR) to be a potent poor survival predictor for cervical cancer have also been evaluated. [9][10][11] As one of the two isoforms of the key enzyme in the biosynthesis of prostaglandins, 12 COX-2 plays an important role in tumor progression, such as cell proliferation, apoptosis inhibition, angiogenesis, invasiveness and immunosuppression. [13][14][15] Multiple studies 5,8,[16][17][18][19][2...