Division of Medical Oncology, Oncology department, Hospital Costa del Sol, Autovía A-7, Km 187, C. P. 29603, Marbella, Malaga, Spain.
Clin Transl Oncol. 2012 Sep;14(9):682-8. doi: 10.1007/s12094-012-0859-2. Epub 2012 Jul 24.
Cyclooxygenase-2 (COX2) is an enzyme that plays a role in different stages of the carcinogenic process and has prognostic and predictive values that have not yet been established. The objective of this study was to evaluate the role of COX2 overexpression in advanced squamous cell carcinoma of the larynx that has been treated with a phonation conservation protocol.
This study included a retrospective analysis of 59 patients with resectable tumours that were treated with chemotherapy (CT) and/or radiation therapy (RT). The expression levels of COX2, epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF), and vascular endothelial growth factor receptor (VEGFR-2) in collected biopsy specimens were determined via immunohistochemistry.
Forty-four percent of the included samples demonstrated overexpression of COX2. In the statistical analysis, COX2 overexpression did not correlate with other clinical or treatment efficacy prognostic factors; however, the median global survival (OS) of patients whose tumours expressed COX2 was 79 months, whereas COX2-negative patients had a median OS of only 38 months, although this finding did not reach statistical significance. The other analysed biological parameters did not demonstrate a significant relationship with COX2.
COX2 overexpression was a common finding in our study. The results obtained did not reveal relationships with established prognostic categories; however, the difference in survival between patients with and without COX2 expression justifies the need for future prospective studies that utilise a larger patient sample size.
环氧化酶-2(COX2)是一种在致癌过程的不同阶段发挥作用的酶,其预后和预测价值尚未确定。本研究的目的是评估 COX2 过表达在接受保声协议治疗的晚期喉鳞状细胞癌中的作用。
本研究回顾性分析了 59 例可切除肿瘤患者,这些患者接受了化疗(CT)和/或放射治疗(RT)。通过免疫组织化学测定收集的活检标本中 COX2、表皮生长因子受体(EGFR)、血管内皮生长因子(VEGF)和血管内皮生长因子受体(VEGFR-2)的表达水平。
44%的纳入样本显示 COX2 过表达。在统计学分析中,COX2 过表达与其他临床或治疗效果预后因素无关;然而,COX2 阳性肿瘤患者的中位总生存期(OS)为 79 个月,而 COX2 阴性患者的中位 OS 仅为 38 个月,尽管这一发现没有达到统计学意义。其他分析的生物学参数与 COX2 之间没有显示出显著的相关性。
COX2 过表达在我们的研究中是一种常见的发现。所获得的结果与既定的预后分类没有关系;然而,COX2 表达阳性和阴性患者的生存差异证明需要进行未来的前瞻性研究,以使用更大的患者样本量。