Department of Psychological Sciences, University of Liverpool, Liverpool, L69 3GB, UK.
Liverpool Ocular Oncology Centre, Liverpool University Hospitals NHS Foundation Trust, Liverpool, Merseyside, L7 8XP, UK.
J Behav Med. 2022 Feb;45(1):115-123. doi: 10.1007/s10865-021-00252-8. Epub 2021 Aug 27.
A number of patient-reported outcomes (PROs) predict increased mortality after primary cancer treatment. Studies, though, are sometimes affected by methodological limitations. They often use control variables that poorly predict life expectancy, examine only one or two PROs thus not controlling potential confounding by unmeasured PROs, and observe PROs at only a single point in time. To predict all-cause mortality, this study used control variables affording good estimates of life expectancy, conducted multivariate analyses of multiple PROs to identify independent predictors, and monitored PROs two years after diagnosis. We recruited a consecutive sample of 824 patients with uveal melanoma between April 2008 and December 2014. PROs were variables shown to predict mortality in previous studies; anxiety, depression, visual and ocular symptoms, visual function impairment, worry about cancer recurrence, and physical, emotional, social and functional quality of life (QoL), measured 6, 12 and 24 months after diagnosis. We conducted Cox regression analyses with a census date of December 2018. Covariates were age, gender, marital and employment status, self-reported co-morbidities, tumor diameter and thickness, treatment modality and chromosome 3 mutation status, the latter a genetic mutation strongly associated with mortality. Single predictor analyses (with covariates), showed 6-month depression and poorer functional QoL predicting mortality, as did 6-12 month increases in anxiety and 6-12 month decreases in physical and functional QoL. Multivariate analyses using all PROs showed independent prediction by 6-month depression and decreasing QoL over 6-12 months and 12-24 months. Elevated depression scores six months post-diagnosis constituted an increased mortality risk. Early intervention for depressive symptoms may reduce mortality.
一些患者报告的结局(PROs)可预测原发性癌症治疗后的死亡率增加。然而,这些研究有时受到方法学限制的影响。它们经常使用无法很好预测预期寿命的对照变量,只检查一个或两个 PROs,因此无法控制未测量的 PROs 引起的潜在混杂,并且仅在一个时间点观察 PROs。为了预测全因死亡率,本研究使用了能够很好地估计预期寿命的对照变量,对多个 PROs 进行了多变量分析,以确定独立的预测因素,并在诊断后两年监测 PROs。我们招募了 2008 年 4 月至 2014 年 12 月期间连续的 824 例葡萄膜黑色素瘤患者。PROs 是先前研究中显示可预测死亡率的变量;焦虑、抑郁、视觉和眼部症状、视觉功能障碍、担心癌症复发以及身体、情感、社会和功能生活质量(QoL),在诊断后 6、12 和 24 个月进行测量。我们使用 2018 年 12 月的普查日期进行 Cox 回归分析。协变量为年龄、性别、婚姻和就业状况、自我报告的合并症、肿瘤直径和厚度、治疗方式和 3 号染色体突变状态,后者是与死亡率密切相关的基因突变。单因素分析(有协变量)显示,6 个月时的抑郁和较差的功能 QoL 预测死亡率,6-12 个月时的焦虑增加和 6-12 个月时的身体和功能 QoL 下降也是如此。使用所有 PROs 的多因素分析显示,6 个月时的抑郁和 6-12 个月和 12-24 个月期间 QoL 的下降具有独立的预测作用。诊断后 6 个月时抑郁评分升高构成了死亡风险增加。早期干预抑郁症状可能会降低死亡率。