Urology and Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
BJU Int. 2011 Jul;108(1):31-7. doi: 10.1111/j.1464-410X.2010.09854.x. Epub 2010 Nov 24.
• To assess the expression pattern of cyclooxygenase-2 (COX-2) in bilharzial and non-bilharzial related bladder cancer (BBC and NBBC) and its association with clinical outcome after radical cystectomy (RC). We also determined the clinico-pathological differences between BBC and NBBC.
• Immunohistochemical (IHC) staining for COX-2 was performed on archival bladder specimens from 315 patients treated with RC between 1997 and 2003. • Patients were divided into 2 groups: Group 1 comprised 205 patients (65%) with BBC and group 2 comprised 110 patients (35%) with NBBC. • Clinico-pathological differences were compared and altered IHC expression of COX-2 was correlated with clinical outcome in both groups.
• The study included 315 patients (239 males and 76 females) with median age 54 y (range 31-79) and median follow up of 63.2 months after RC. • There was significant difference in histological types, tumor stage, grade, and architecture and COX-2 alterations between both groups (P < 0.05). • BBC presented with lower grade, higher stage, and non-papillary non-urothelial carcinoma. COX-2 overexpression was associated with pathological T stage (P= 0.01), grade (P < 0.001) and lymphovascular invasion (LVI) (P= 0.041). • COX-2 expression was an independent predictor of disease recurrence (HR 1.9, CI 0.99-3.626 and P= 0.05) and cancer specific mortality (HR 2.8, CI 1.155-6.73 and P= 0.023) only in BBC but not in NBBC (HR 1.6, CI 0.598-4.364, P= 0.344 and HR 0.349, CI 0.076-1.595, P= 0.175, respectively).
• BBC differs pathologically and biologically from NBBC. BBCs present more frequently as low-grade, high stage non-papillary and non-urothelial cancers. BBCs with COX-2 alterations are associated with worse outcome after RC. • Our findings support the need for further evaluation of COX-2 and inflammatory signaling pathways as well as COX-2-targeted prevention and therapies in BC.
评估环氧化酶-2(COX-2)在埃及血吸虫和非埃及血吸虫相关膀胱癌(BBC 和 NBBC)中的表达模式及其与根治性膀胱切除术(RC)后临床结果的关系。我们还确定了 BBC 和 NBBC 之间的临床病理差异。
对 1997 年至 2003 年间接受 RC 治疗的 315 名患者的存档膀胱标本进行免疫组织化学(IHC)染色。患者分为 2 组:第 1 组包括 205 名(65%)BBC 患者,第 2 组包括 110 名(35%)NBBC 患者。比较临床病理差异,并比较 COX-2 的改变 IHC 表达与两组的临床结果。
该研究包括 315 名患者(239 名男性和 76 名女性),中位年龄 54 岁(范围 31-79 岁),RC 后中位随访时间为 63.2 个月。两组间组织学类型、肿瘤分期、分级和结构以及 COX-2 改变存在显著差异(P<0.05)。BBC 表现为低级别、高级别和非乳头非尿路上皮癌。COX-2 过表达与病理 T 分期(P=0.01)、分级(P<0.001)和血管淋巴管侵犯(LVI)(P=0.041)相关。COX-2 表达仅在 BBC 中是疾病复发(HR 1.9,CI 0.99-3.626,P=0.05)和癌症特异性死亡率(HR 2.8,CI 1.155-6.73,P=0.023)的独立预测因素,但在 NBBC 中则不是(HR 1.6,CI 0.598-4.364,P=0.344 和 HR 0.349,CI 0.076-1.595,P=0.175)。
BBC 在病理和生物学上与 NBBC 不同。BBC 更常表现为低级别、高级别、非乳头和非尿路上皮癌。COX-2 改变的 BBC 与 RC 后不良结局相关。我们的研究结果支持进一步评估 COX-2 和炎症信号通路,以及 COX-2 靶向预防和治疗膀胱癌。