Weiss Christian, von Römer Felix, Capalbo Gianni, Ott Oliver J, Wittlinger Michael, Krause Steffen F, Sauer Rolf, Rödel Claus, Rödel Franz
Department of Radiation Oncology, Johann Wolfgang Goethe-University, Frankfurt/Main, Germany.
Int J Radiat Oncol Biol Phys. 2009 Aug 1;74(5):1455-60. doi: 10.1016/j.ijrobp.2008.10.063. Epub 2009 Feb 21.
The objectives of this study were to investigate the expression of survivin in tumor samples from patients with high-risk T1 bladder cancer and to correlate its expression with clinicopathologic features as well as clinical outcomes after initial transurethral resection (TURBT) followed by radiotherapy (RT) or radiochemotherapy (RCT).
Survivin protein expression was evaluated by immunohistochemistry on tumor specimen (n = 48) from the initial TURBT, and was correlated with clinical and histopathologic characteristics as well as with 5-year rates of local failure, tumor progression, and death from urothelial cancer after primary bladder sparring treatment with RT/RCT.
Survivin was not expressed in normal bladder urothelium but was overexpressed in 67% of T1 tumors. No association between survivin expression and clinicopathologic factors (age, gender, grading, multifocality, associated carcinoma in situ) could be shown. With a median follow-up of 27 months (range, 3-140 months), elevated survivin expression was significantly associated with an increased probability of local failure after TURBT and RCT/RT (p = 0.003). There was also a clear trend toward a higher risk of tumor progression (p = 0.07) and lower disease-specific survival (p = 0.10).
High survivin expression is a marker of tumor aggressiveness and may help to identify a subgroup of patients with T1 bladder cancer at a high risk for recurrence when treated with primary organ-sparing approaches such as TURBT and RCT.
本研究的目的是调查高危T1期膀胱癌患者肿瘤样本中生存素的表达情况,并将其表达与临床病理特征以及初次经尿道膀胱肿瘤切除术(TURBT)后放疗(RT)或放化疗(RCT)后的临床结局相关联。
通过免疫组织化学对初次TURBT获取的肿瘤标本(n = 48)评估生存素蛋白表达,并将其与临床和组织病理学特征以及RT/RCT初次膀胱保留治疗后5年的局部失败、肿瘤进展和尿路上皮癌死亡发生率相关联。
生存素在正常膀胱尿路上皮中不表达,但在67%的T1期肿瘤中过度表达。生存素表达与临床病理因素(年龄、性别、分级、多灶性、伴发原位癌)之间未显示出相关性。中位随访27个月(范围3 - 140个月),生存素表达升高与TURBT及RCT/RT后局部失败概率增加显著相关(p = 0.003)。肿瘤进展风险更高(p = 0.07)和疾病特异性生存率更低(p = 0.10)也有明显趋势。
生存素高表达是肿瘤侵袭性的标志物,可能有助于识别T1期膀胱癌患者中采用TURBT和RCT等原发性器官保留方法治疗时复发风险高的亚组。