Lerner S E, Seay T M, Blute M L, Bergstralh E J, Barrett D, Zincke H
Department of Urology, Mayo Clinic, Rochester, Minnesota 55905, USA.
J Urol. 1996 Mar;155(3):821-6.
The majority of impalpable prostate cancers (state T1c) are biologically significant. We report the interim results in 257 patients with stage T1c prostate cancer treated with radical prostatectomy.
Prostate specific antigen progression-free survival was assessed by the Kaplan-Meier method. Multivariate analyses were performed to determine which clinical and pathological variables independently correlated with progression. Comparisons among the various clinical substages (T1a to T2b/c) were calculated.
Of the patients with stage T1c cancers 51% had stage pT2c or less and 91% had clinically significant tumors on the basis of pathological grade, deoxyribonucleic acid ploidy and tumor volume. High preoperative prostate specific antigen, poorly differentiated tumors and nondiploid status were strong independent predictors of progression. The 5-year survival rate free of progression was 84%. Patients with clinical stage T1c cancers had a significant progression-free survival advantage compared to those with clinical stage T2b/c disease (p = 0.0005).
Impalpable tumors should not be regarded as insignificant or innocuous on the basis of pathological analysis. Disease-free survival in the stage T1c group was similar to that in the clinical stages T1a to T2a group but significantly better than that in the T2b/c group.
大多数无法触及的前列腺癌(T1c期)具有生物学意义。我们报告了257例接受根治性前列腺切除术的T1c期前列腺癌患者的中期结果。
采用Kaplan-Meier法评估无前列腺特异性抗原进展生存期。进行多变量分析以确定哪些临床和病理变量与进展独立相关。计算了不同临床亚分期(T1a至T2b/c)之间的比较结果。
在T1c期癌症患者中,51%为pT2c期或更低分期,91%根据病理分级、脱氧核糖核酸倍体和肿瘤体积具有临床意义的肿瘤。术前前列腺特异性抗原水平高、肿瘤分化差和非二倍体状态是进展的强有力独立预测因素。5年无进展生存率为84%。与临床分期为T2b/c期的患者相比,临床分期为T1c期癌症的患者具有显著的无进展生存优势(p = 0.0005)。
基于病理分析,不可触及的肿瘤不应被视为无意义或无害。T1c期组的无病生存期与临床分期T1a至T2a组相似,但明显优于T2b/c组。