Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard Unit 97, Houston, TX 77030-4009, USA.
Eur J Cancer. 2012 Jul;48(11):1664-71. doi: 10.1016/j.ejca.2012.01.026. Epub 2012 Feb 13.
A competing risks analysis was undertaken to identify subgroups at greatest risk of dying from prostate cancer (PC) after definitive external beam radiation therapy (RT)±androgen deprivation therapy (ADT) in the prostate specific antigen (PSA) era.
Outcomes of 2675 men with localised PC treated with RT±ADT from 1987-2007 were analysed. Prostate cancer-specific mortality (PCSM) and non-PCSM rates were calculated after stratifying patients according to National Comprehensive Cancer Network (NCCN) risk-group, RT dose, use of ADT and age at treatment.
Only 0.2% of low-risk men died of PC 10 years after treatment. All of these deaths occurred in patients treated with < 72 Gy, and only one patient ≥ 70 years old who received ≥ 72 Gy died of PC at last follow-up. Likewise, none of the patients with intermediate-risk disease treated with ≥ 72 Gy and ADT died of PC at 10 years, and the highest 10-year rate of PCSM was seen in men ≥ 70 years old treated with < 72 Gy without ADT (5.1%). Among high-risk men < 70 years old, treatment with RT dose < 72 Gy without ADT yielded similar 10-year rates of PCSM (15.2%) and non-PCSM (18.5%), whereas men treated with ≥ 72 Gy and ADT were twice as likely to die from other causes (16.2%) than PC (9.4%). In high-risk men ≥ 70 years old, dose-escalation with ADT reduced 10-year PCSM from 14% to 4%, and most deaths were due to other causes.
Low- and intermediate-risk patients treated with definitive RT are unlikely to die of PC. PCSM is higher in men with high-risk disease but may be reduced with dose-escalation and ADT, although patients are still twice as likely to die of other causes.
在 PSA 时代,采用外照射放疗(RT)±雄激素剥夺疗法(ADT)治疗局限性前列腺癌(PC)后,为确定死于 PC 的风险最高的亚组人群,我们进行了一项竞争风险分析。
分析了 1987 年至 2007 年间接受 RT±ADT 治疗的 2675 例局限性 PC 患者的结局。按照国家综合癌症网络(NCCN)风险组、RT 剂量、ADT 使用情况和治疗时的年龄对患者进行分层,计算 PC 特异性死亡率(PCSM)和非 PC 死亡率。
只有 0.2%的低危男性在治疗 10 年后死于 PC。所有这些死亡均发生于接受<72Gy 治疗的患者中,且在最后一次随访中,仅有一名≥70 岁、接受≥72Gy 治疗的患者死于 PC。同样,接受≥72Gy 和 ADT 治疗的中危患者在 10 年内均无死于 PC,在未接受 ADT 治疗、接受<72Gy 放疗且年龄≥70 岁的男性中,PCSM 的最高 10 年发生率为 5.1%。对于年龄<70 岁的高危男性,若不接受 ADT,接受<72Gy 的 RT 剂量治疗,10 年 PCSM 发生率(15.2%)和非 PC 死亡率(18.5%)相似,而接受≥72Gy 和 ADT 治疗的男性死于其他原因的可能性是死于 PC 的两倍(16.2%对 9.4%)。对于年龄≥70 岁的高危男性,采用 ADT 剂量递增可将 10 年 PCSM 从 14%降至 4%,且大多数死亡归因于其他原因。
采用确定性 RT 治疗的低危和中危患者不太可能死于 PC。高危患者的 PCSM 较高,但通过剂量递增和 ADT 可能降低,尽管患者死于其他原因的可能性仍是死于 PC 的两倍。