Hirao Y, Ozono S, Momose H, Okajima E, Hiramatsu T, Yoshida K, Fukushima S, Ohashi Y
Department of Urology, Nara Medical University, Japan.
Cancer Chemother Pharmacol. 1994;35 Suppl:S36-40. doi: 10.1007/BF00686917.
The preliminary results of a multi-institutional prospective randomized study of the prophylaxis of superficial bladder cancer using epirubicin (protocol NUORG SBT-003) are reported. The subjects were 129 patients with untreated superficial bladder cancer (< or = T1b, < or = G2) who were randomized into 2 groups: a transurethral resection (TUR)-alone group (63 patients) and a TUR + intravesical epirubicin (20 mg/40 ml, 30 times/2 years) group (66 patients). The nonrecurrence rate observed in the epirubicin group was significantly higher than that seen in the control group. To unify the pathological diagnosis, a central pathology laboratory (CPL) was set up for extramural review. The correspondence of the pathological diagnosis of TUR-Bt specimens between the CPL and the local pathology laboratory (LPL) was 70.5% in grading and 51.9% in staging. There was a tendency for overdiagnosis by the LPL for both the grade and the stage of tumors. However, differing interpretations by pathologists seem to exert little influence on the nonrecurrence rate at interim analysis. Further observation will be necessary to clarify the prophylactic efficacy of low-dose, long-term periodic intravesical epirubicin instillation and the influence of the disagreement in pathological findings between the CPL and the LPL on the analysis of the results.
本文报告了一项关于使用表柔比星预防浅表性膀胱癌的多机构前瞻性随机研究(方案编号NUORG SBT - 003)的初步结果。研究对象为129例未经治疗的浅表性膀胱癌患者(≤T1b,≤G2),这些患者被随机分为两组:单纯经尿道切除术(TUR)组(63例患者)和TUR + 膀胱内灌注表柔比星(20 mg/40 ml,每2年30次)组(66例患者)。表柔比星组观察到的无复发率显著高于对照组。为统一病理诊断,设立了一个中心病理实验室(CPL)进行外部审核。CPL与当地病理实验室(LPL)对TUR - Bt标本的病理诊断在分级上的符合率为70.5%,在分期上的符合率为51.9%。LPL在肿瘤分级和分期方面均存在过度诊断的倾向。然而,在中期分析中,病理学家的不同解读似乎对无复发率影响不大。需要进一步观察以明确低剂量、长期定期膀胱内灌注表柔比星的预防效果以及CPL与LPL之间病理结果差异对结果分析的影响。