Rödel C, Grabenbauer G G, Rödel F, Birkenhake S, Kühn R, Martus P, Zörcher T, Fürsich D, Papadopoulos T, Dunst J, Schrott K M, Sauer R
Department of Radiation Oncology, University of Erlangen-Nürnberg, Erlangen, Germany.
Int J Radiat Oncol Biol Phys. 2000 Mar 15;46(5):1213-21. doi: 10.1016/s0360-3016(99)00544-1.
Several groups have reported the value of bladder preservation by a combined treatment protocol, including transurethral resection (TUR-B) and radiochemotherapy (RCT). As more experience is acquired with organ-sparing treatment, patient selection should be optimized. The purpose of this study was to investigate the role of several biologic markers that may predict response to RCT in muscle-invasive bladder carcinoma.
The apoptotic index (AI), Ki-67, p53, and bcl-2 were evaluated by immunohistochemistry on pretreatment biopsies from 70 patients treated for invasive bladder cancer by TUR-B and RCT. Expression of each marker was correlated with initial response, local control, and cancer-specific survival with preserved bladder. An exploratory multivariate analysis was also performed that included clinical and immunohistochemical variables.
A high AI (> median = 1.6%) and a high Ki-67 index (> median = 8.8%), but not the p53- and bcl-2 expression, were significantly related to initial complete response (CR) and local control with preserved bladder after 5 years. When the AI and Ki-67 expression were considered simultaneously, the association with initial CR (p < 0. 001), local control (p = 0.0002), and cancer-specific survival with preserved bladder (p = 0.008) was highly significant. In an exploratory multivariate analysis (final model), only AI, Ki-67, and the combined AI/Ki-67 variable retained significance for local control with preserved bladder at 5 years.
Patients with a high spontaneous AI and a high pretreatment Ki-67 index should be considered preferentially for treatment with RCT, whereas tumors with low proliferation and low levels of apoptosis are less likely to respond to RCT.
多个研究小组报道了通过包括经尿道切除术(TUR - B)和放化疗(RCT)的联合治疗方案来保留膀胱的价值。随着器官保留治疗经验的增加,患者选择应得到优化。本研究的目的是调查几种生物学标志物在预测肌层浸润性膀胱癌对RCT反应中的作用。
通过免疫组织化学对70例接受TUR - B和RCT治疗的浸润性膀胱癌患者的治疗前活检组织进行凋亡指数(AI)、Ki - 67、p53和bcl - 2评估。每种标志物的表达与初始反应、局部控制以及保留膀胱的癌症特异性生存率相关。还进行了一项探索性多变量分析,包括临床和免疫组化变量。
高AI(>中位数 = 1.6%)和高Ki - 67指数(>中位数 = 8.8%),而非p53和bcl - 2表达,与初始完全缓解(CR)以及5年后保留膀胱的局部控制显著相关。当同时考虑AI和Ki - 67表达时,与初始CR(p < 0.001)、局部控制(p = 0.0002)以及保留膀胱的癌症特异性生存率(p = 0.008)的关联非常显著。在探索性多变量分析(最终模型)中,仅AI、Ki - 67以及联合的AI/Ki - 67变量对5年后保留膀胱的局部控制具有显著意义。
自发AI高且治疗前Ki - 67指数高的患者应优先考虑接受RCT治疗,而增殖低且凋亡水平低的肿瘤对RCT反应的可能性较小。