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Explained variation of excess hazard models

机译:过度危害模型的解释性变化

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摘要

The availability of longstanding collection of detailed cancer patient information makes multivariable modelling of cancer‐specific hazard of death appealing. We propose to report variation in survival explained by each variable that constitutes these models. We adapted the ranks explained (RE) measure to the relative survival data setting, ie, when competing risks of death are accounted for through life tables from the general population. RE is calculated at each event time. We introduce weights for each death reflecting its probability to be a cancer death. RE varies between −1 and +1 and can be reported at given times in the follow‐up and as a time‐varying measure from diagnosis onward. We present an application for patients diagnosed with colon or lung cancer in England. The RE measure shows reasonable properties and is comparable in both relative and cause‐specific settings. One year after diagnosis, RE for the most complex excess hazard models reaches 0.56, 95% CI: 0.54 to 0.58 (0.58 95% CI: 0.56–0.60) and 0.69, 95% CI: 0.68 to 0.70 (0.67, 95% CI: 0.66–0.69) for lung and colon cancer men (women), respectively. Stage at diagnosis accounts for 12.4% (10.8%) of the overall variation in survival among lung cancer patients whereas it carries 61.8% (53.5%) of the survival variation in colon cancer patients. Variables other than performance status for lung cancer (10%) contribute very little to the overall explained variation. The proportion of the variation in survival explained by key prognostic factors is a crucial information toward understanding the mechanisms underpinning cancer survival. The time‐varying RE provides insights into patterns of influence for strong predictors.
机译:长期收集的详细癌症患者信息的可用性使对癌症特定的死亡危险的多变量建模具有吸引力。我们建议报告由构成这些模型的每个变量解释的生存变异。我们根据相对生存数据设置调整了解释等级(RE)度量,即当通过一般人群的生命表考虑死亡竞争风险时。 RE是在每个事件时间计算的。我们为每个死亡引入权重,以反映其可能死于癌症的可能性。 RE在-1和+1之间变化,可以在随访中的给定时间报告,并且可以作为诊断以后的随时间变化的措施。我们为英国诊断出患有结肠癌或肺癌的患者提出申请。 RE度量显示出合理的属性,并且在相对设置和特定原因设置中均具有可比性。诊断后一年,对于最复杂的过度危害模型,RE达到0.56、95%CI:0.54至0.58(0.58 95%CI:0.56-0.60)和0.69、95%CI:0.68至0.70(0.67、95%CI:肺癌和结肠癌男性(女性)分别为0.66-0.69)。诊断阶段占肺癌患者总生存变异的12.4%(10.8%),而结肠癌患者占生存总变异的61.8%(53.5%)。除了肺癌的表现状态外,其他变量(10%)对解释的总体变化影响很小。关键预后因素解释的生存率差异是了解癌症生存机制的关键信息。随时间变化的RE提供了对强大预测变量影响模式的见解。

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