Martiniclinic, Prostate Cancer Center Hamburg-Eppendorf, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
Int J Urol. 2010 Oct;17(10):862-8. doi: 10.1111/j.1442-2042.2010.02615.x. Epub 2010 Aug 31.
To examine the rate of Gleason sum upgrading (GSU) from a sum of 6 to a Gleason sum of ≥7 in patients undergoing radical prostatectomy (RP), who fulfilled the recommendations for low dose rate brachytherapy (Gleason sum 6, prostate-specific antigen ≤10 ng/mL, clinical stage ≤T2a and prostate volume ≤50 mL), and to test the performance of an existing nomogram for prediction of GSU in this specific cohort of patients.
The analysis focused on 414 patients, who fulfilled the European Society for Therapeutic Radiation and Oncology and American Brachytherapy Society criteria for low dose rate brachytherapy (LD-BT) and underwent a 10-core prostate biopsy followed by RP. The rate of GSU was tabulated and the ability of available clinical and pathological parameters for predicting GSU was tested. Finally, the performance of an existing GSU nomogram was explored.
The overall rate of GSU was 35.5%. When applied to LD-BT candidates, the existing nomogram was 65.8% accurate versus 70.8% for the new nomogram. In decision curve analysis tests, the new nomogram fared substantially better than the assumption that no patient is upgraded and better than the existing nomogram.
GSU represents an important issue in LD-BT candidates. The new nomogram might improve patient selection for LD-BT and cancer control outcome by excluding patients with an elevated probability of GSU.
检查接受根治性前列腺切除术(RP)的患者中,符合低剂量率近距离放射治疗(Gleason 评分 6,前列腺特异性抗原≤10ng/mL,临床分期≤T2a 和前列腺体积≤50mL)建议的患者中,Gleason 评分从 6 增加到≥7 的升级率,并测试现有列线图预测该特定患者队列中升级的性能。
该分析集中在 414 名符合欧洲治疗放射肿瘤学会和美国近距离放射治疗学会低剂量率近距离放射治疗(LD-BT)标准的患者,这些患者接受了 10 芯前列腺活检,随后进行了 RP。列出了 Gleason 升级率,并测试了预测 Gleason 升级的现有临床和病理参数的能力。最后,探讨了现有的 Gleason 升级列线图的性能。
总体升级率为 35.5%。当应用于 LD-BT 候选者时,现有的列线图的准确性为 65.8%,而新的列线图为 70.8%。在决策曲线分析测试中,新的列线图表现明显优于不升级任何患者的假设,也优于现有的列线图。
GSU 是 LD-BT 候选者的一个重要问题。新的列线图可能通过排除升级概率较高的患者来改善 LD-BT 和癌症控制结果的患者选择。