Cooperberg Matthew R, Cowan Janet, Broering Jeannette M, Carroll Peter R
Department of Urology, Program in Urologic Oncology, Urologic Outcomes Research Group, UCSF Comprehensive Cancer Center, University of California, San Francisco, CA 94115-1711, USA.
World J Urol. 2008 Jun;26(3):211-8. doi: 10.1007/s00345-008-0250-7. Epub 2008 Mar 28.
This study aimed to describe national trends in presentation, management, and outcomes for men with high risk prostate cancer.
Data were abstracted from CaPSURE; 10,808 men were diagnosed between 1990 and 2007 and had complete clinical data. High-risk was defined according to the D'Amico criteria; a more restrictive definition assigned clinical stage T2c to intermediate rather than high risk. Temporal trends were assessed for patient distribution among risk groups, and within the high-risk group for individual risk factors, Kattan nomogram score, Cancer of the Prostate Risk Assessment (CAPRA) score, and primary treatment. Survival analysis stratified by CAPRA score was performed.
Under the standard definition, 31.2% of the men were diagnosed with high-risk disease, and 16.9% were high-risk under the restrictive definition. This proportion has fallen over time but has been stable since 2000. Patients who would be stratified to high risk under the standard definition and to intermediate risk under the restrictive definition have better outcomes than those stratified to either intermediate or high risk under both definitions. There has been no consistent risk migration within the high-risk group over time. Treatment varies substantially with CAPRA score within the high-risk group, with higher risk men less likely to receive local therapy. Use of androgen deprivation therapy has increased over time, both as primary therapy and in conjunction with both external beam radiation and brachytherapy. Biochemical outcomes vary according to CAPRA score within the high-risk group.
Clinical stage T2c should not define high risk, and the high-risk group should be substratified using a multivariable instrument. There is no evidence for meaningful downward risk migration among high-risk patients over the past 15 years. At least some men in the high-risk group may be undertreated.
本研究旨在描述高危前列腺癌男性患者在就诊、治疗及预后方面的全国性趋势。
数据取自CaPSURE;1990年至2007年间确诊的10808名男性患者拥有完整的临床数据。高危根据达米科标准定义;更严格的定义将临床分期T2c归为中危而非高危。评估了风险组间患者分布的时间趋势,以及高危组内个体风险因素、卡坦列线图评分、前列腺癌风险评估(CAPRA)评分和初始治疗的时间趋势。进行了按CAPRA评分分层的生存分析。
按照标准定义,31.2%的男性被诊断为高危疾病,按照严格定义则为16.9%。这一比例随时间下降,但自2000年以来保持稳定。在标准定义下被分层为高危而在严格定义下为中危的患者,其预后优于在两种定义下均被分层为中危或高危的患者。高危组内随时间并无一致的风险转移。高危组内治疗因CAPRA评分差异很大,风险较高的男性接受局部治疗的可能性较小。雄激素剥夺治疗的使用随时间增加,既作为初始治疗,也与外照射放疗和近距离放疗联合使用。高危组内生化预后因CAPRA评分而异。
临床分期T2c不应定义为高危,高危组应使用多变量工具进行亚分层。过去15年中,没有证据表明高危患者中有有意义的向下风险转移。高危组中至少有部分男性可能治疗不足。