College of Medicine & Health, University of Exeter, Exeter, Devon, UK
Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
BMJ Open. 2021 Feb 12;11(2):e044420. doi: 10.1136/bmjopen-2020-044420.
To confirm the association of previously reported prognostic factors with future progression of localised prostate cancer using primary care data and identify new potential prognostic factors for further assessment in prognostic model development and validation.
Retrospective cohort study, employing Cox proportional hazards regression controlling for age, prostate specific antigen (PSA), and Gleason score, was stratified by diagnostic stage.
Primary care in England.
Males with localised prostate cancer diagnosedbetween 01/01/1987 and 31/12/2016 within the Clinical Practice ResearchDatalink database, with linked data from the National Cancer Registration andAnalysis Service and Office for National Statistics.
Primary outcome measure was prostate cancer mortality. Secondary outcome measures were all-cause mortality and commencing systemic therapy. Up-staging after diagnosis was not used as a secondary outcome owing to significant missing data.
10 901 men (mean age 74.38±9.03 years) with localised prostate cancer were followed up for a mean of 14.12 (±6.36) years. 2331 (21.38%) men underwent systemic therapy and 3450 (31.65%) died, including 1250 (11.47%) from prostate cancer. Factors associated with an increased risk of prostate cancer mortality included age; high PSA; current or ex-smoker; ischaemic heart disease; high C reactive protein; high ferritin; low haemoglobin; high blood glucose and low albumin.
This study identified several new potential prognostic factors for prostate cancer progression, as well as confirming some known prognostic factors, in an independent primary care data set. Further research is needed to develop and validate a prognostic model for prostate cancer progression.
利用初级保健数据证实先前报道的预后因素与局限性前列腺癌的未来进展之间的关联,并确定新的潜在预后因素,以进一步评估在预后模型的开发和验证中。
回顾性队列研究,采用 Cox 比例风险回归控制年龄、前列腺特异性抗原(PSA)和 Gleason 评分,按诊断阶段分层。
英格兰的初级保健。
1987 年 1 月 1 日至 2016 年 12 月 31 日期间在临床实践研究数据链接数据库中诊断为局限性前列腺癌的男性,与国家癌症登记和分析服务以及国家统计局的相关数据链接。
主要结局指标是前列腺癌死亡率。次要结局指标是全因死亡率和开始系统治疗。由于数据缺失严重,诊断后升级未用作次要结局。
10901 名(平均年龄 74.38±9.03 岁)局限性前列腺癌患者平均随访 14.12(±6.36)年。2331 名(21.38%)男性接受了系统治疗,3450 名(31.65%)死亡,包括 1250 名(11.47%)死于前列腺癌。与前列腺癌死亡率增加相关的因素包括年龄;高 PSA;当前或曾吸烟者;缺血性心脏病;高 C 反应蛋白;高铁蛋白;低血红蛋白;高血糖和低白蛋白。
本研究在独立的初级保健数据集内确定了几个新的潜在前列腺癌进展预后因素,同时也证实了一些已知的预后因素。需要进一步研究来开发和验证前列腺癌进展的预后模型。