Ali-El-Dein B, Sarhan O, Hinev A, Ibrahiem El-H I, Nabeeh A, Ghoneim M A
Urology and Nephrology Center, Mansoura University, Egypt.
BJU Int. 2003 Sep;92(4):393-9. doi: 10.1046/j.1464-410x.2003.04360.x.
To assess the prognostic factors that could be used to predict tumour recurrence and progression, and to construct and validate a predictive index.
Between June 1991 and December 2000, 533 patients (418 men and 115 women; mean age 55.4 years) underwent complete transurethral resection of histologically confirmed pTa and pT1 transitional cell carcinoma of the bladder, after which 377 (test series) were randomized into two subsequent studies, of six groups, to receive adjuvant intravesical sequential bacillus Calmette-Guérin (BCG) and epirubicin, BCG alone, epirubicin (50 or 80 mg), adriamycin 50 mg or no adjuvant therapy. Factors potentially affecting tumour recurrence or progression were assessed using univariate and multivariate analysis, i.e. tumour stage, histological grade, DNA ploidy, history of recurrence, multiplicity, size, tumour configuration, associated carcinoma in situ, recurrence at the first 3-month check cystoscopy and the use of adjuvant therapy. The regression coefficients determined by Cox regression analysis were used to construct a predictive index (PI). The algebraic sum of the regression coefficients of the factors with independent and significant association with disease-free survival for each case represented a proportional hazard score (PHS). The PI was validated in another series of 156 patients (validation series) in whom the same regression coefficients for the same significant factors as the test series were used to categorize it into three risk groups. Kaplan-Meier survival curves were plotted to compare the different risk categories in both test and validation series.
The mean (sd, range) follow-up in the test and validation series were 58 (19, 5-96) and 28.3 (14.9, 2-94) months, respectively. In the test series, tumour stage, DNA ploidy, multiplicity, history of recurrence, tumour configuration, cystoscopy result and the type of adjuvant therapy had independent significance for recurrence on multivariate analysis. For progression, the cystoscopy result, DNA ploidy and grade were the only independent and significant predictors. The ranges of PHS for the factors affecting recurrence-free and progression-free survival were 0.0-7.14 and 0.0-5.84, respectively, which were divided equally into three risk categories with significant differences on Kaplan-Meier curves and a log-rank test (P < 0.001). The three categories in the validation series were significantly different from each other and each was comparable with that in the test series.
Tumour stage, DNA ploidy, multiplicity, history of recurrence, tumour configuration and type of adjuvant therapy affected independently the rate of recurrence after resecting superficial bladder tumour. Recurrence at the 3-month cystoscopy, histological grade and DNA ploidy were the only predictors of progression to muscle-invasion. The PI dividing the patients into three risk groups with different treatment and follow-up strategies for recurrence and progression was reproducible in a validation series.
评估可用于预测肿瘤复发和进展的预后因素,并构建和验证一个预测指数。
1991年6月至2000年12月期间,533例患者(418例男性和115例女性;平均年龄55.4岁)接受了经组织学证实的膀胱pTa和pT1期移行细胞癌的完全经尿道切除术,之后377例(试验组)被随机分为后续两项研究中的六个组,分别接受辅助膀胱内序贯卡介苗(BCG)和表柔比星、单纯BCG、表柔比星(50或80mg)、阿霉素50mg或不进行辅助治疗。使用单因素和多因素分析评估可能影响肿瘤复发或进展的因素,即肿瘤分期、组织学分级、DNA倍体、复发史、肿瘤数量、大小、肿瘤形态、伴发原位癌、首次3个月膀胱镜检查时的复发情况以及辅助治疗的使用。通过Cox回归分析确定的回归系数用于构建预测指数(PI)。每个病例中与无病生存有独立且显著关联的因素的回归系数的代数和代表一个比例风险评分(PHS)。在另一组156例患者(验证组)中验证该PI,使用与试验组相同的显著因素的相同回归系数将其分为三个风险组。绘制Kaplan-Meier生存曲线以比较试验组和验证组中不同的风险类别。
试验组和验证组的平均(标准差,范围)随访时间分别为58(19,5 - 96)个月和28.3(14.9,2 - 94)个月。在试验组中,多因素分析显示肿瘤分期、DNA倍体、肿瘤数量、复发史、肿瘤形态、膀胱镜检查结果和辅助治疗类型对复发具有独立意义。对于进展而言,膀胱镜检查结果、DNA倍体和分级是仅有的独立且显著的预测因素。影响无复发生存和无进展生存的因素的PHS范围分别为0.0 - 7.14和0.0 - 5.84,将其等分为三个风险类别,在Kaplan-Meier曲线和对数秩检验中有显著差异(P < 0.001)。验证组中的三个类别彼此之间有显著差异,且每个类别与试验组中的类别具有可比性。
肿瘤分期、DNA倍体、肿瘤数量、复发史、肿瘤形态和辅助治疗类型独立影响浅表膀胱肿瘤切除术后的复发率。3个月膀胱镜检查时的复发、组织学分级和DNA倍体是进展至肌层浸润的唯一预测因素。将患者分为具有不同复发和进展治疗及随访策略的三个风险组的PI在验证组中具有可重复性。