Hitchings A W, Kumar M, Jordan S, Nargund V, Martin J, Berney D M
Department of Histopathology and Morbid Anatomy, Bart's & The London School of Medicine & Dentistry, St Bartholomew's Hospital, West Smithfield, London EC1A 7BE, UK.
Br J Cancer. 2004 Aug 2;91(3):552-7. doi: 10.1038/sj.bjc.6601954.
Currently available prognostic tools appear unable to adequately predict recurrence and progression in non muscle-invasive bladder carcinomas. We aimed to assess the prognostic value of immunohistochemical evaluation of the cell cycle markers p53, p16 and pRb. Paraffin blocks were obtained from 78 cases of pTa and pT1 transitional cell carcinomas, for which long-term follow-up was available. Representative sections were stained using antibodies against p53, p16 and pRb. Altered marker expression was found in 45, 17 and 30% of cases, respectively. Concurrent alteration of two or three markers occurred in 19% of cases, and was significantly associated with grade and stage. In univariate survival analysis, the concurrent alteration of any two markers was significantly associated with progression. The greatest risk was produced by alteration of both p53 and p16, which increased the risk of progression by 14.45 times (95% confidence interval (CI) 3.10-67.35). After adjusting for grade and stage, this risk was 7.73 (CI 1.13-52.70). The markers did not generally predict tumour recurrence, except in the 25 pT1 tumours. In these, p16 alteration was associated with a univariate risk of 2.83 (CI 1.01-7.91), and concurrent p53 and p16 alteration with a risk of 9.29 (CI 1.24-69.50). Overall, we conclude that the immunohistochemical evaluation of p53 and p16 may have independent prognostic value for disease progression, and may help guide management decisions in these tumours.
目前可用的预后工具似乎无法充分预测非肌层浸润性膀胱癌的复发和进展。我们旨在评估细胞周期标志物p53、p16和pRb免疫组化评估的预后价值。从78例有长期随访资料的pTa和pT1移行细胞癌中获取石蜡块。使用抗p53、p16和pRb的抗体对代表性切片进行染色。分别在45%、17%和30%的病例中发现标志物表达改变。19%的病例出现两种或三种标志物同时改变,且与分级和分期显著相关。在单因素生存分析中,任何两种标志物同时改变与进展显著相关。p53和p16同时改变产生的风险最大,进展风险增加了14.45倍(95%置信区间(CI)3.10 - 67.35)。在对分级和分期进行校正后,该风险为7.73(CI 1.13 - 52.70)。这些标志物一般不能预测肿瘤复发,但在25例pT1肿瘤中除外。在这些肿瘤中,p16改变的单因素风险为2.83(CI 1.01 - 7.91),p53和p16同时改变的风险为9.29(CI 1.24 - 69.50)。总体而言,我们得出结论,p53和p16的免疫组化评估可能对疾病进展具有独立的预后价值,并可能有助于指导这些肿瘤的管理决策。