Matthes Katarina Luise, Limam Manuela, Pestoni Giulia, Held Leonhard, Korol Dimitri, Rohrmann Sabine
Division of Chronic Disease Epidemiology, Institute for Epidemiology, Biostatistics and Prevention, University of Zurich, Zurich, Switzerland.
Cancer Registry Zurich and Zug, University Hospital Zurich, Vogelsangstrasse 10, 8091, Zurich, Switzerland.
J Cancer Res Clin Oncol. 2018 Apr;144(4):707-715. doi: 10.1007/s00432-018-2596-6. Epub 2018 Feb 7.
The aim of this study was to assess the associations of comorbidities with primary treatment of prostate cancer (PCa) patients and of comorbidities with PCa-specific mortality (PCSM) compared to other-cause mortality (OCM) in Switzerland.
We included 1527 men diagnosed with PCa in 2000 and 2001 in the canton of Zurich. Multiple imputation methods were applied to missing data for stage, grade and comorbidities. Multinomial logistic regression analyses were used to explore the associations of comorbidities with treatment. Cox regression models were used to estimate all-cause mortality, and Fine and Gray competing risk regression models to estimate sub-distribution hazard ratios for the outcomes PCSM and OCM.
Increasing age was associated with a decreasing probability of receiving curative treatment, whereas an increasing Charlson Comorbidity Index (CCI) did not influence the treatment decision as strongly as age. The probability of OCM was higher for patients with comorbidities compared to those without comorbidities [CCI 1: hazard ratio 2.07 (95% confidence interval 1.51-2.85), CCI 2+: 2.34 (1.59-3.44)]; this was not observed for PCSM [CCI 1: 0.79 (0.50-1.23), CCI 2+: 0.97 (0.59-1.59)]. In addition, comorbidities had a greater impact on the patients' mortality than age.
The results of the current study suggest that chronological age is a stronger predictor of treatment choices than comorbidities, although comorbidities have a larger influence on patients' mortality. Hence, inclusion of comorbidities in treatment choices may provide more appropriate treatment for PCa patients to counteract over- or undertreatment.
本研究旨在评估瑞士前列腺癌(PCa)患者的合并症与初始治疗之间的关联,以及合并症与前列腺癌特异性死亡率(PCSM)和其他原因死亡率(OCM)之间的关联。
我们纳入了2000年和2001年在苏黎世州被诊断为PCa的1527名男性。对分期、分级和合并症的缺失数据采用多重填补方法。采用多项逻辑回归分析来探讨合并症与治疗之间的关联。采用Cox回归模型估计全因死亡率,采用Fine和Gray竞争风险回归模型估计PCSM和OCM结局的亚分布风险比。
年龄增加与接受根治性治疗的概率降低相关,而Charlson合并症指数(CCI)增加对治疗决策的影响不如年龄大。与无合并症的患者相比,合并症患者的OCM概率更高[CCI 1:风险比2.07(95%置信区间1.51 - 2.85),CCI 2+:2.34(1.59 - 3.44)];PCSM未观察到这种情况[CCI 1:0.79(0.50 - 1.23),CCI 2+:0.97(0.59 - 1.59)]。此外,合并症对患者死亡率的影响大于年龄。
本研究结果表明,尽管合并症对患者死亡率的影响更大,但实际年龄比合并症更能预测治疗选择。因此,在治疗选择中纳入合并症可能为PCa患者提供更合适的治疗,以避免过度治疗或治疗不足。