Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Cancer Epidemiology Unit, Department of Medical Sciences, University of Turin, Turin, Italy.
Am J Epidemiol. 2019 Jun 1;188(6):1165-1173. doi: 10.1093/aje/kwz026.
In this paper, we describe the Prognostic Factors for Mortality in Prostate Cancer (ProMort) study and use it to demonstrate how the weighted likelihood method can be used in nested case-control studies to estimate both relative and absolute risks in the competing-risks setting. ProMort is a case-control study nested within the National Prostate Cancer Register (NPCR) of Sweden, comprising 1,710 men diagnosed with low- or intermediate-risk prostate cancer between 1998 and 2011 who died from prostate cancer (cases) and 1,710 matched controls. Cause-specific hazard ratios and cumulative incidence functions (CIFs) for prostate cancer death were estimated in ProMort using weighted flexible parametric models and compared with the corresponding estimates from the NPCR cohort. We further drew 1,500 random nested case-control subsamples of the NPCR cohort and quantified the bias in the hazard ratio and CIF estimates. Finally, we compared the ProMort estimates with those obtained by augmenting competing-risks cases and by augmenting both competing-risks cases and controls. The hazard ratios for prostate cancer death estimated in ProMort were comparable to those in the NPCR. The hazard ratios for dying from other causes were biased, which introduced bias in the CIFs estimated in the competing-risks setting. When augmenting both competing-risks cases and controls, the bias was reduced.
在本文中,我们描述了前列腺癌死亡率预后因素(ProMort)研究,并利用它展示如何在嵌套病例对照研究中使用加权似然法来估计竞争风险环境下的相对风险和绝对风险。ProMort 是一项嵌套在瑞典国家前列腺癌登记处(NPCR)中的病例对照研究,包含 1710 名 1998 年至 2011 年间被诊断为低危或中危前列腺癌且死于前列腺癌的男性(病例)和 1710 名匹配对照。使用加权灵活参数模型在 ProMort 中估计了前列腺癌死亡的特异性危险比和累积发病率函数(CIF),并与 NPCR 队列中的相应估计值进行了比较。我们进一步从 NPCR 队列中随机抽取了 1500 个嵌套病例对照子样本,并量化了危险比和 CIF 估计值的偏倚。最后,我们将 ProMort 的估计值与通过增加竞争风险病例和同时增加竞争风险病例和对照获得的估计值进行了比较。ProMort 估计的前列腺癌死亡率的危险比与 NPCR 中的相似。死于其他原因的危险比存在偏差,这导致竞争风险环境下估计的 CIF 存在偏差。当同时增加竞争风险病例和对照时,偏差会减少。