Department of Oncology, Cumming School of Medicine, University of Calgary, 3300 Hospital Drive NW, Calgary, AB, T2N 4N1, Canada.
Department of Oncology, Cumming School of Medicine, University of Calgary, 3300 Hospital Drive NW, Calgary, AB, T2N 4N1, Canada; Tom Baker Cancer Centre, Alberta Health Services, 1331 29th Street, NW, Calgary, AB, T2N 4N2, Canada.
Lung Cancer. 2019 Aug;134:141-146. doi: 10.1016/j.lungcan.2019.06.003. Epub 2019 Jun 6.
To investigate how clinical, demographic and treatment-related factors in non-small cell lung cancer (NSCLC) patients impact the risk of mortality in the 30 days following receipt of systemic anti-cancer therapies (SACT), and undertake a comprehensive review of the treatment decisions and experiences of a real-world population.
We reviewed NSCLC patients receiving SACT from 2005 to 2014, and captured in the Glans-Look Lung Cancer Database, which contains demographic, clinical, pathological, treatment and outcome data. The 30-day post-SACT mortality rate was calculated, and regimen changes in the last 14 days of life were identified. Univariate analysis and multivariate logistic regression were used to identify demographic, tumor and treatment-related factors that correlated with mortality risk.
1044 patients receiving ≥ 1 cycle of SACT in 2005-2014 were identified. 233 (22.3%) deaths occurred ≤ 30 days following SACT receipt; 32 (13.7%) of which had new SACT regimens ≤ 14 days prior to death. Risk of 30-day mortality and regimen changes at the end of life increased in association with being male [OR: 1.48 (1.12-1.95), p = 0.005], advanced disease at diagnosis [OR: 1.85 (1.19-2.88), p = 0.006], palliative-intent treatment [OR: 6.75 (3.88-11.77), p < 0.001], and use of EGFR-targeting agents [OR: 4.5 (3.27-6.18) p < 0.001]. Risk of early mortality decreased for never-smokers [OR: 0.62 (0.41-0.95), p = 0.028], and those receiving SACT in more recent years (2010-2014) [OR: 0.65 (0.49-0.86), p = 0.002].
Our findings identified several factors that affected the risk of early mortality in NSCLC patients following SACT. These results from a representative population provide insights regarding the benefits and risks of SACT and can serve to inform clinical and palliative best practices.
研究非小细胞肺癌(NSCLC)患者的临床、人口统计学和治疗相关因素如何影响接受全身抗癌治疗(SACT)后 30 天内的死亡率,并对真实人群的治疗决策和经验进行全面回顾。
我们回顾了 2005 年至 2014 年间接受 SACT 的 NSCLC 患者,并在 Glans-Look 肺癌数据库中捕获了人口统计学、临床、病理、治疗和结局数据。计算了 SACT 后 30 天的死亡率,并确定了生命最后 14 天的方案变化。使用单因素分析和多因素逻辑回归来确定与死亡率风险相关的人口统计学、肿瘤和治疗相关因素。
在 2005-2014 年期间,确定了 1044 名接受至少 1 个周期 SACT 的患者。SACT 后≤30 天内有 233 例(22.3%)死亡;其中 32 例(13.7%)在死亡前≤14 天内接受了新的 SACT 方案。30 天死亡率和生命结束时方案变化的风险随着男性[比值比(OR):1.48(1.12-1.95),p=0.005]、诊断时晚期疾病[OR:1.85(1.19-2.88),p=0.006]、姑息治疗意图[OR:6.75(3.88-11.77),p<0.001]和表皮生长因子受体靶向药物的使用[OR:4.5(3.27-6.18),p<0.001]而增加。从不吸烟者[OR:0.62(0.41-0.95),p=0.028]和最近几年(2010-2014 年)接受 SACT 的患者[OR:0.65(0.49-0.86),p=0.002]的早期死亡率风险降低。
我们的研究结果确定了一些影响 NSCLC 患者接受 SACT 后早期死亡风险的因素。来自代表性人群的这些结果提供了关于 SACT 的获益和风险的见解,并有助于为临床和姑息治疗提供最佳实践。