Institute of Pathology, HELIOS Clinic Bad Saarow, Bad Saarow, Germany.
J Urol. 2012 Mar;187(3):899-907. doi: 10.1016/j.juro.2011.10.149. Epub 2012 Jan 15.
We assessed the prognostic role of p16(INK4a) expression in penile cancer with respect to cancer specific survival.
Based on a multi-institutional collaboration wax embedded tissues from 92 surgically treated patients, including 27 with total and 65 with partial penectomy, were retrospectively evaluated. After a central histopathological review by 1 pathologist a tissue microarray was constructed for p16(INK4a) immunostaining. Two independent pathologists evaluated p16(INK4a) expression, which was correlated with cancer specific survival. The κ statistic was used to assess interobserver variability. Univariate and multivariate Cox proportional hazards analysis was applied to assess the independent effects of prognostic factors on cancer specific survival during a median postoperative followup of 32 months (IQR 6-66).
The κ statistic revealed excellent interobserver agreement (κ 0.934, p <0.001). Two and 5-year cancer specific survival rates for the entire study cohort were 86% and 74%, respectively. The 2 and 5-year rates for patients without and with p16(INK4a) expression differed significantly (73% and 57% vs 95% and 85%, respectively, p = 0.011). Univariate analysis revealed p16(INK4a) expression as a significant prognostic factor with respect to cancer specific survival (p = 0.018). Multivariate analysis identified koilocytosis (HR 0.24, 95% CI 0.07-0.83, p = 0.024), p16(INK4a) expression (HR 0.44, 95% CI 0.23-0.84, p = 0.013), and histological stage (HR 3.54, 95% CI 1.88-6.67, p <0.001) and grade (HR 2.47, 95% CI 1.00-6.09, p = 0.049) as independent prognostic factors for cancer specific survival.
Results show that p16(INK4a) seems to be a prognostic parameter for primary invasive penile cancer with excellent interobserver reproducibility. At pathology laboratories without antibodies against p16(INK4a) conventional histological determination of koilocytosis by the pathologist also appears to provide important prognostic information for cancer specific survival.
我们评估了 p16(INK4a)在阴茎癌中的表达与癌症特异性生存的关系。
基于多机构合作,对 92 例接受手术治疗的患者的蜡包埋组织进行了回顾性评估,其中 27 例接受了全切除术,65 例接受了部分切除术。在 1 名病理学家进行中央病理复查后,构建了 p16(INK4a)免疫组化组织微阵列。2 名独立的病理学家评估了 p16(INK4a)的表达情况,并与癌症特异性生存相关。使用 κ 统计量评估观察者间的变异性。应用单变量和多变量 Cox 比例风险分析评估预后因素对癌症特异性生存的独立影响,术后中位随访时间为 32 个月(IQR 6-66)。
κ 统计量显示观察者间的一致性极好(κ=0.934,p<0.001)。整个研究队列的 2 年和 5 年癌症特异性生存率分别为 86%和 74%。无 p16(INK4a)表达和有 p16(INK4a)表达的患者 2 年和 5 年的生存率差异有统计学意义(分别为 73%和 57%比 95%和 85%,p=0.011)。单变量分析显示 p16(INK4a)表达是癌症特异性生存的一个显著预后因素(p=0.018)。多变量分析显示挖空细胞(HR 0.24,95%CI 0.07-0.83,p=0.024)、p16(INK4a)表达(HR 0.44,95%CI 0.23-0.84,p=0.013)、组织学分期(HR 3.54,95%CI 1.88-6.67,p<0.001)和分级(HR 2.47,95%CI 1.00-6.09,p=0.049)是癌症特异性生存的独立预后因素。
结果表明,p16(INK4a)似乎是原发性浸润性阴茎癌的一个预后参数,具有极好的观察者间可重复性。在没有针对 p16(INK4a)的抗体的病理实验室中,病理学家对挖空细胞的常规组织学确定似乎也为癌症特异性生存提供了重要的预后信息。