医学
置信区间
相对存活率
比例危险模型
危险系数
前列腺癌
人口
内科学
流行病学
预期寿命
肿瘤科
癌症
癌症登记处
环境卫生
作者
Francesco Di Bello,Letizia Maria Ippolita Jannello,Andrea Baudo,Mario de Angelis,Carolin Siech,Zhe Tian,Jordan A. Goyal,Massimiliano Creta,Gianluigi Califano,Giuseppe Celentano,Pietro Acquati,Fred Saad,Shahrokh F. Shariat,Luca Carmignani,Ottavio De Cobelli,Alberto Briganti,Felix K. H. Chun,Nicola Longo,Pierre I. Karakiewicz
摘要
ABSTRACT Objective To quantify the differences in 5‐year overall survival (OS) between high‐grade (Gleason sum 8–10) incidental prostate cancer (IPCa) patients and age‐matched male population‐based controls, according to treatment type: no active versus active treatment. Materials and Methods We relied on the Surveillance, Epidemiology, and End Results (SEER) database (2004–2015) to identify not actively treated and actively treated high‐grade IPCa patients. For each case, we simulated an age‐matched male control (Monte Carlo simulation), relying on Social Security Administration Life Tables (2004–2020) with 5 years of follow‐up. Additionally, we relied on Kaplan–Meier plots to display OS for each treatment type. Multivariable Cox regression models were fitted to predict overall mortality (OM). Results Of 564 high‐grade IPCa patients, 345 (61%) were not actively treated versus 219 (39%) were actively treated, either with radical prostatectomy or radiotherapy. Median OS was 3 years for not actively treated high‐grade IPCa patients, with OS difference at 5 years follow‐up of 27% relative to their age‐matched male population‐based controls (37% vs. 64%). Median OS was 8 years for actively treated high‐grade IPCa patients, with OS difference at 5 years follow‐up of 6% relative to their age‐matched male population‐based controls (68% vs. 74%). In the multivariable Cox regression model, active treatment independently predicted lower OM (hazard ratio = 0.6; 95% confidence interval = 0.4–0.8; p < 0.001). Conclusion Relative to Life Tables' derived age‐matched male controls, not actively treated high‐grade IPCa patients exhibit drastically worse OS than their actively treated counterparts. These observations may encourage clinicians to consider active treatment in newly diagnosed high‐grade IPCa patients.
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