Berg Kasper Drimer, Thomsen Frederik Birkebæk, Mikkelsen Marta K, Ingimarsdóttir Inga J, Hansen Rikke B, Kejs Anne Mette T, Brasso Klaus
Copenhagen Prostate Cancer Center, Department of Urology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark; Department of Urology, Zealand University Hospital, Roskilde, Denmark.
Copenhagen Prostate Cancer Center, Department of Urology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark; Department of Urology, Bispebjerg and Frederiksberg Hospital, Frederiksberg, Denmark.
Eur J Cancer. 2017 Feb;72:20-27. doi: 10.1016/j.ejca.2016.11.025. Epub 2016 Dec 23.
During recent years, several new life-prolonging therapeutic options have been introduced for patients with metastatic prostate cancer (mPCa). The aim of the present study was to evaluate the changes in the survival of patients diagnosed with mPCa prior to and in the early period of the implementation of these new agents.
The study population consisted of 207 men diagnosed in 1997 and 316 men diagnosed in the period 2007-2013 with de novo mPCa and managed with initial endocrine therapy. Men were followed for overall survival and PCa-specific survival.
At the time of diagnosis, men diagnosed in the period 2007-2013 had less co-morbidity, lower prostrate-specific antigen levels and lower clinical tumour categories than men diagnosed in 1997. A significantly higher proportion of men diagnosed in 1997 were managed with surgical castration (57% versus 9%). Only one patient diagnosed in 1997 received second-line therapy compared with 81 men (26%) diagnosed in the period 2007-2013. The median overall survival was significantly longer for men diagnosed between 2007 and 2013 compared with men diagnosed in 1997 (39.4 months versus 24.2 months, p < 0.0001). Likewise, the cumulative incidence of PCa-specific death was higher among men diagnosed in 1997 compared with men diagnosed between 2007 and 2013, with 5-year cumulative incidences of 72% and 47%, respectively (p < 0.0001).
Survival in men diagnosed with metastatic PCa has improved significantly over time. The improved survival can in part be explained by lead-time bias, but also by the introduction of new life-prolonging treatments.
近年来,针对转移性前列腺癌(mPCa)患者引入了几种新的延长生命的治疗选择。本研究的目的是评估在这些新药物实施之前及实施早期被诊断为mPCa的患者的生存变化。
研究人群包括1997年诊断的207名男性和2007 - 2013年期间诊断为新发mPCa并接受初始内分泌治疗的316名男性。对男性进行总生存和前列腺癌特异性生存随访。
在诊断时,2007 - 2013年期间诊断的男性比1997年诊断的男性合并症更少、前列腺特异性抗原水平更低且临床肿瘤类别更低。1997年诊断的男性接受手术去势治疗的比例显著更高(57%对9%)。1997年诊断的患者中只有1例接受二线治疗,而2007 - 2013年期间诊断的有81名男性(26%)接受二线治疗。2007年至2013年诊断的男性的中位总生存时间显著长于1997年诊断的男性(39.4个月对24.2个月,p < 0.0001)。同样,1997年诊断的男性中前列腺癌特异性死亡的累积发生率高于2007年至2013年诊断的男性,5年累积发生率分别为72%和47%(p < 0.0001)。
随着时间的推移,被诊断为转移性前列腺癌的男性的生存情况有了显著改善。生存改善部分可归因于领先时间偏倚,但也归因于新的延长生命治疗方法的引入。