Denzinger Stefan, Fritsche Hans-Martin, Otto Wolfgang, Blana Andreas, Wieland Wolf-Ferdinand, Burger Maximilian
Department of Urology, University of Regensburg, Regensburg, Germany.
Eur Urol. 2008 Jan;53(1):146-52. doi: 10.1016/j.eururo.2007.06.030. Epub 2007 Jun 27.
We compared long-term outcome in patients with initial pT1G3 bladder cancer (BC) treated with early versus deferred cystectomy (CX) for recurrent pT1G3 or muscle-invasive BC after an initial bladder-sparing approach. The aim of this study was to compare survival rates and to analyse the influence of the recognised risk factors multifocality, tumour size, and carcinoma in situ (CIS) in initial transurethral resection of the bladder.
Between 1995 and 2005, a total of 105 patients were diagnosed with initial pT1G3 BC featuring>or=2 risk factors. Forty-five percent had multiple tumours, 73% tumours>3 cm in size, and 46% CIS. All patients were offered early CX. Fifty-one percent of patients opted for early and 49% underwent deferred CX for recurring BC. Risk factors were distributed evenly between the groups.
Upstaging in the CX specimen was found in 30% of cases. No risk factor was related to upstaging. The 10-yr cancer-specific survival rate was 78% in early CX and 51% in deferred CX (p<0.01). No risk factor predicted cancer-related death in early CX. In survival analysis, CIS was related to a lower cancer-specific survival rate in deferred CX (p<0.001).
Early as opposed to deferred CX seems to prolong the cancer-specific survival rate in high-risk pT1G3 BC. Patients with CIS should be considered for early CX owing to reduced cancer-specific survival in case of deferred CX.
我们比较了初始采用保留膀胱方法治疗的pT1G3期膀胱癌(BC)患者,在出现复发性pT1G3或肌层浸润性BC后,早期与延期行膀胱切除术(CX)的长期预后。本研究的目的是比较生存率,并分析在初次经尿道膀胱肿瘤切除术中,多灶性、肿瘤大小和原位癌(CIS)这些公认的风险因素的影响。
1995年至2005年期间,共有105例被诊断为初始pT1G3期BC且具有≥2个风险因素的患者。45%有多发肿瘤,73%肿瘤大小>3 cm,46%有CIS。所有患者均被建议早期行CX。51%的患者选择早期CX,49%因复发性BC接受延期CX。风险因素在两组间分布均匀。
CX标本中发现30%的病例有分期上升。没有风险因素与分期上升相关。早期CX组的10年癌症特异性生存率为78%,延期CX组为51%(p<0.01)。在早期CX组中,没有风险因素可预测癌症相关死亡。在生存分析中,CIS与延期CX组较低的癌症特异性生存率相关(p<0.001)。
与延期CX相比,早期CX似乎能提高高危pT1G3期BC患者的癌症特异性生存率。由于延期CX会降低癌症特异性生存率,对于有CIS的患者应考虑早期CX。