Zincke H
Department of Urology, Mayo Clinic, Rochester, MN 55905.
NCI Monogr. 1988(7):109-15.
Limited clinical stage C (T3 NX M0) disease can be treated surgically, and morbidity can be acceptable. When appropriate adjuvant therapy (orchiectomy and/or radiation) is administered, residual cancer can be controlled locally for at least a limited period. The incidence of local progression in pathologic stage C or D1 disease may be negligible after early adjuvant orchiectomy and/or radiation treatment. The combination of immediate orchiectomy and radical prostatectomy has been shown to limit progression significantly (P = .0009) in many patients with D1 (T0-3 N1,2 M0) disease. However, some patients do not respond to this combination treatment, which suggests that systemic dissemination of heterogeneous tumor cells is unresponsive to adjuvant androgen ablation therapy. The DNA ploidy pattern may be a valuable predictor of disease outcome after treatment in stage D1 disease. Other pathologic variables (including acid phosphatase levels) have not been useful in predicting disease outcome or treatment response. Finally, patients with limited clinical stage C disease and those with pathologic C or D1 disease should be enrolled in a prospective randomized protocol so that the possible beneficial effects of adjuvant treatment programs can be evaluated. Apart from the usual pathologic variables and prostate-specific antigen testing, the DNA pattern should be included as a stratification factor.
临床分期局限的C期(T3 NX M0)疾病可通过手术治疗,且发病率可接受。当给予适当的辅助治疗(睾丸切除术和/或放疗)时,残留癌可在局部得到至少有限时间的控制。在早期进行辅助睾丸切除术和/或放疗后,病理分期为C期或D1期疾病的局部进展发生率可能微不足道。对于许多D1期(T0 - 3 N1,2 M0)疾病患者,立即进行睾丸切除术和根治性前列腺切除术的联合已显示能显著限制疾病进展(P = .0009)。然而,一些患者对这种联合治疗无反应,这表明异质性肿瘤细胞的全身播散对辅助性雄激素剥夺治疗无反应。DNA倍体模式可能是D1期疾病治疗后疾病结局的一个有价值的预测指标。其他病理变量(包括酸性磷酸酶水平)在预测疾病结局或治疗反应方面并无用处。最后,临床分期局限的C期疾病患者以及病理分期为C期或D1期疾病的患者应纳入前瞻性随机试验方案,以便评估辅助治疗方案可能的有益效果。除了常规的病理变量和前列腺特异性抗原检测外,DNA模式应作为一个分层因素纳入。