Cancer Survival Group, London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK.
Department of Biostatistics and Medical Informatics, University of Llubljana, Vrazov trg 2, SI-1000, Ljubljana, Slovenia.
Stat Med. 2018 Jun 30;37(14):2284-2300. doi: 10.1002/sim.7645. Epub 2018 Apr 6.
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.
长期收集详细的癌症患者信息使得对癌症特异性死亡风险的多变量建模变得很有吸引力。我们建议报告构成这些模型的每个变量对生存的解释变异。我们将解释的秩(RE)度量方法应用于相对生存数据设置,即在考虑一般人群生命表中死亡的竞争风险时。RE 是在每个事件时间计算的。我们为每个死亡引入了权重,以反映其为癌症死亡的概率。RE 的范围在-1 到+1 之间,可以在随访的特定时间报告,也可以作为从诊断开始的时变度量报告。我们展示了在英格兰诊断为结肠癌或肺癌的患者的应用。RE 度量具有合理的特性,在相对和病因特异性设置中都具有可比性。诊断后 1 年,最复杂的超额危险模型的 RE 达到 0.56,95%CI:0.54-0.58(0.58 95%CI:0.56-0.60)和 0.69,95%CI:0.68-0.70(0.67,95%CI:0.66-0.69),分别为男性(女性)肺癌和结肠癌患者。诊断时的分期占肺癌患者总生存变异的 12.4%(10.8%),而结肠癌患者的生存变异占 61.8%(53.5%)。除了肺癌的表现状态外,其他变量(10%)对整体解释变异的贡献很小。生存的关键预后因素所解释的变异比例是了解癌症生存机制的重要信息。时变的 RE 提供了对强预测因子影响模式的深入了解。