Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Department of Epidemiology, CancerCare Manitoba, Winnipeg, Manitoba, Canada.
J Geriatr Oncol. 2022 Jun;13(5):654-661. doi: 10.1016/j.jgo.2022.02.015. Epub 2022 Mar 4.
Frailty impacts outcomes for patients with lung cancer, but no brief tools have been assessed in patients with metastatic disease. We evaluated the impact of the Modified Frailty Index (mFI) on clinical outcomes for patients with metastatic non-small cell lung cancer (NSCLC).
We conducted a retrospective cohort study of all patients with Stage IV NSCLC diagnosed in Manitoba between 2011 and 2016 who then received first-line cytotoxic chemotherapy. We assigned mFI scores based on documented comorbidities and collected data on toxicity, progression, and survival. Descriptive statistics characterized the cohort and toxicity experienced. Kaplan-Meier methods were used to evaluate progression-free survival (PFS) and overall survival (OS), followed by multivariable Cox proportional hazards models.
Our cohort of 426 (mFI 0/1-2/3+ = 175/196/55) patients, showed no significant association between higher mFI score and incidence of overall chemotherapy toxicity. Patients with mFI 0 experienced more frequent thromboses (p=0.022) and a trend towards less nausea or vomiting (p = 0.059). There was no significant difference in PFS or OS among frailty groups. Poorer performance status, number of metastatic sites, and the absence of a driver mutation were independently associated with poorer PFS and OS. Male sex and not completing chemotherapy were also associated with worse OS.
This study is the first to investigate the use of the mFI as a frailty tool in patients with metastatic NSCLC receiving cytotoxic chemotherapy. The mFI does not appear to be strongly associated with treatment-related toxicities, PFS, or OS in patients with metastatic NSCLC receiving first-line cytotoxic chemotherapy.
虚弱对肺癌患者的预后有影响,但尚未评估转移疾病患者的简短工具。我们评估了改良虚弱指数(mFI)对转移性非小细胞肺癌(NSCLC)患者临床结局的影响。
我们对 2011 年至 2016 年间在马尼托巴省诊断为 IV 期 NSCLC 并随后接受一线细胞毒性化疗的所有患者进行了回顾性队列研究。我们根据记录的合并症分配 mFI 评分,并收集毒性、进展和生存数据。描述性统计数据描述了队列和所经历的毒性。使用 Kaplan-Meier 方法评估无进展生存期(PFS)和总生存期(OS),然后进行多变量 Cox 比例风险模型分析。
我们的 426 例患者队列(mFI 0/1-2/3+ = 175/196/55),mFI 评分较高与总体化疗毒性发生率之间无显著关联。mFI 0 组患者更频繁地发生血栓形成(p=0.022),且恶心或呕吐的发生率较低(p = 0.059)。虚弱组之间的 PFS 或 OS 无显著差异。较差的表现状态、转移性部位的数量以及缺乏驱动突变与较差的 PFS 和 OS 独立相关。男性和未完成化疗也与较差的 OS 相关。
这项研究是首次调查 mFI 在接受细胞毒性化疗的转移性 NSCLC 患者中作为虚弱工具的使用。在接受一线细胞毒性化疗的转移性 NSCLC 患者中,mFI 似乎与治疗相关毒性、PFS 或 OS 无明显关联。