First Department of Respiratory Medicine, Nanjing Chest Hospital, Nanjing, China.
J Thorac Dis. 2013 Feb;5(1):40-7. doi: 10.3978/j.issn.2072-1439.2013.01.02.
Cyclooxygenase-2 (COX-2) has been implicated in tumorigenesis and metastasis, and it presumably mediates the proliferation of endothelial cells and promotes vascular permeability. However, the prognostic value of COX-2 overexpression in patients with non-small cell lung cancer (NSCLC) remains controversial.
A systematic review of eligible studies with meta-analysis was performed to quantitatively review the correlation of COX-2 overexpression with survival in patients with NSCLC.
We conducted a final analysis of 1,892 patients from 16 studies. The studies were categorized by histology, disease stage, patient race and laboratory techniques used. Combined hazard ratios (HR) suggested that COX-2 overexpression was not associated with a significant impact on survival, the HR (95% CI) was 0.90 (95% CI: 0.76-1.04) overall, 0.99 (0.71-1.26) in Asian patients, 0.87 (0.71-1.03) in non-Asian patients, 0.63 (0.33-0.93) in adenocarcinoma, 1.42 (1.02-1.81) in stage I NSCLC, 0.83 (0.72-1.08) in NSCLC by IHC, 3.28 (1.48-5.13) in NSCLC by RT-PCR.
COX-2 overexpression seems to have no significant impact on survival of NSCLC patients. However, the statistically significant was found in stage I NSCLC, suggesting that COX-2 expression could be useful at early stages to distinguish those with a worse prognosis.
环氧化酶-2(COX-2)已被牵涉到肿瘤发生和转移中,它可能介导内皮细胞的增殖,并促进血管通透性。然而,COX-2 过表达在非小细胞肺癌(NSCLC)患者中的预后价值仍存在争议。
我们进行了一项系统的文献回顾和荟萃分析,以定量评估 COX-2 过表达与 NSCLC 患者生存的相关性。
我们对来自 16 项研究的 1892 名患者进行了最终分析。这些研究按组织学、疾病分期、患者种族和使用的实验室技术进行分类。合并的危险比(HR)表明,COX-2 过表达与生存无显著相关性,总 HR(95%CI)为 0.90(95%CI:0.76-1.04),亚洲患者为 0.99(0.71-1.26),非亚洲患者为 0.87(0.71-1.03),腺癌为 0.63(0.33-0.93),I 期 NSCLC 为 1.42(1.02-1.81),免疫组化(IHC)为 0.83(0.72-1.08),逆转录聚合酶链反应(RT-PCR)为 3.28(1.48-5.13)。
COX-2 过表达似乎对 NSCLC 患者的生存没有显著影响。然而,在 I 期 NSCLC 中发现了统计学上的显著差异,这表明 COX-2 表达在早期阶段可能有助于区分预后较差的患者。