Helgstrand John Thomas, Røder Martin Andreas, Klemann Nina, Toft Birgitte Grønkær, Brasso Klaus, Vainer Ben, Iversen Peter
Copenhagen Prostate Cancer Center, Department of Urology, Copenhagen University Hospital, Rigshospitalet, University of Copenhagen, Ole maaløes vej 24, Section 7521, DK-2200 Copenhagen, Denmark.
Department of Pathology, Copenhagen University Hospital, Rigshospitalet, University of Copenhagen, Blegdamsvej 9, DK-2100 Copenhagen, Denmark.
Eur J Cancer. 2017 Oct;84:18-26. doi: 10.1016/j.ejca.2017.07.007. Epub 2017 Aug 2.
The diagnostic characteristics of men who eventually die from prostate cancer (PCa) and the extent to which early diagnostic strategies have affected these characteristics are unclear. We aimed to investigate trends in survival and clinical presentation at diagnosis in men who eventually died from PCa.
Based on the national database, the Danish Prostate Cancer Registry, a nationwide population-based study of all 19,487 men who died from PCa in Denmark between 1995 and 2013 was conducted. Trends in median survival and trends in age, prostate-specific antigen (PSA), clinical stage, and Gleason score (GS) at diagnosis were analysed.
A total of 46.9%, 16.8%, and 36.3% had metastatic (M+), locally advanced/lymph node positive (LaN+), and localised disease, respectively, at diagnosis. Only 0.15% had localised disease, GS ≤ 6 and PSA<10. Over time, the proportion of men with M+ disease at diagnosis decreased from 54.0-38.3% (p < 0.0001), whereas the proportion LaN + disease increased from 8.6-27.3% (p < 0.0001). The proportion of localised disease remained stable at 33.2-41.9%. Median survival increased 2.11 years from 1.88 (95% CI: 1.68-2.08) in 1995 to 3.99 (95% CI: 3.71-4.28) years in 2013, p < 0.0001.
In a large population-based study, the results confirmed concurrent literature that the majority of men who eventually died from PCa had LaN+ or M+ disease at diagnosis. The proportion of men with M+ disease at diagnosis decreased significantly over time, parallelled by an increase in median survival. Taken together, this indicates a lead-time effect on survival, which presently, however, is not substantial enough to result in a reduced PCa-specific mortality.
最终死于前列腺癌(PCa)的男性的诊断特征以及早期诊断策略对这些特征的影响程度尚不清楚。我们旨在调查最终死于PCa的男性的生存趋势和诊断时的临床表现。
基于丹麦前列腺癌国家注册数据库这一全国性数据库,对1995年至2013年间在丹麦死于PCa的所有19487名男性进行了一项全国性的基于人群的研究。分析了中位生存期趋势以及诊断时的年龄、前列腺特异性抗原(PSA)、临床分期和 Gleason评分(GS)趋势。
诊断时分别有46.9%、16.8%和36.3%的患者出现转移(M+)、局部晚期/淋巴结阳性(LaN+)和局限性疾病。只有0.15%的患者为局限性疾病,GS≤6且PSA<10。随着时间的推移,诊断时患有M+疾病的男性比例从54.0%降至38.3%(p<0.0001),而LaN+疾病的比例从8.6%增至27.3%(p<0.0001)。局限性疾病的比例保持在33.2%至41.9%之间稳定。中位生存期从1995年的1.88年(95%CI:1.68 - 2.08)增加到2013年的3.99年(95%CI:3.71 - 4.28),增加了2.11年,p<0.0001。
在一项大型的基于人群的研究中,结果证实了现有文献,即大多数最终死于PCa的男性在诊断时患有LaN+或M+疾病。诊断时患有M+疾病的男性比例随时间显著下降,同时中位生存期增加。总体而言,这表明对生存有提前期效应,然而目前这种效应还不足以导致PCa特异性死亡率降低。