Genentech, South San Francisco, CA, United States.
Genentech, South San Francisco, CA, United States.
Lung Cancer. 2020 May;143:86-92. doi: 10.1016/j.lungcan.2020.03.005. Epub 2020 Mar 7.
Several obstacles may delay receipt of targeted treatment in patients with anaplastic lymphoma kinase positive (ALK+) non-small-cell lung cancer (NSCLC). This study examined the factors associated with delayed initiation of ALK inhibitor (ALKi) treatment and its impact on overall survival (OS) as well as the impact of initiating chemotherapy before biomarker test results.
Advanced NSCLC (aNSCLC) patients selected from the deidentified Flatiron Health electronic health record-derived database were stratified into early- and delayed-use cohorts based on initiation of ALKi treatment relative to time since receiving ALK+ biomarker test results; cohorts were further stratified by timing of chemotherapy initiation relative to availability of ALK+ test results. Prescription-time matching (PTM) was used to examine the effect of delayed ALKi treatment and chemotherapy on survival; Cox proportional hazards models adjusting for baseline characteristics before and after PTM were used to examine factors associated with delayed ALKi treatment and the effects of delayed ALKi treatment and chemotherapy on OS, respectively.
Comparison of OS between early- and delayed-use cohorts (N = 442 ALK + aNSCLC patients) demonstrated that a >3-week delay in the initiation of ALKi treatment was associated with a >2-fold higher risk of death (adjusted hazard ratio [HR] [95 % CI] 2.05 [1.13, 3.71]. The number of office visits, age factors, and use of chemotherapy were associated with an increased risk of being untreated >3 weeks after ALK+ test results. There were no significant differences in survival outcomes regardless of whether patients received chemotherapy before the ALK+ test result or ALKi treatment (adjusted HR [95 % CI] 1.02 [0.64, 1.63]). Completing the chemotherapy regimen after receiving ALK+ test results did not appear to improve survival (adjusted HR [95 % CI] 0.84 [0.38, 1.9]).
Initiating ALKi treatment for aNSCLC patients in a timely manner may have a positive impact on survival outcomes.
在间变性淋巴瘤激酶阳性(ALK+)非小细胞肺癌(NSCLC)患者中,可能存在多种因素导致靶向治疗延迟。本研究旨在探讨与 ALK 抑制剂(ALKi)治疗延迟相关的因素,以及这些因素对总生存期(OS)的影响,同时还评估了在获得生物标志物检测结果之前开始化疗的影响。
本研究从匿名的 Flatiron Health 电子病历数据库中筛选出晚期 NSCLC(aNSCLC)患者,根据接受 ALK+生物标志物检测结果后开始 ALKi 治疗的时间,将患者分为早期和延迟使用两组;同时根据化疗开始时间与 ALK+检测结果的可获得性进一步分层。采用处方时间匹配(PTM)方法,观察延迟 ALKi 治疗和化疗对生存的影响;采用 Cox 比例风险模型,在 PTM 前后分别调整基线特征,观察与延迟 ALKi 治疗相关的因素,以及延迟 ALKi 治疗和化疗对 OS 的影响。
对 442 例 ALK + aNSCLC 患者的 OS 进行比较,结果显示 ALKi 治疗开始后延迟超过 3 周与死亡风险增加 2 倍以上相关(调整后的风险比[HR] [95%CI]为 2.05 [1.13,3.71])。就诊次数、年龄因素和化疗的使用与 ALK+检测结果后未经治疗的风险增加相关。无论患者是否在 ALK+检测结果之前接受化疗,接受化疗后生存结局均无显著差异(调整后的 HR [95%CI]为 1.02 [0.64,1.63])。在获得 ALK+检测结果后完成化疗方案似乎并未改善生存(调整后的 HR [95%CI]为 0.84 [0.38,1.9])。
及时启动 aNSCLC 患者的 ALKi 治疗可能对生存结局产生积极影响。