Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA; Immuneering Corporation, Cambridge, MA 02142, USA.
Department of Biomedical Data Science, Geisel School of Medicine at Dartmouth, Lebanon, NH 03755, USA; Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH 03755, USA.
Lung Cancer. 2018 Dec;126:89-96. doi: 10.1016/j.lungcan.2018.10.022. Epub 2018 Oct 25.
To measure the association between statin exposure and mortality in lung cancer patients belonging to different categories of histological subtype.
A cohort of 19,974 individuals with incident lung cancer between 2007 and 2011 was identified using the SEER-Medicare linked database. Statin exposure both pre- and post-diagnosis was analyzed to identify a possible association with cancer-specific mortality in patients stratified by histological subtype. Intention-to-treat analyses and time-dependent Cox regression models were used to calculate hazard ratios and 95% confidence intervals (95% CIs) corresponding to statin exposure both pre- and post-diagnosis, respectively.
Overall baseline statin exposure was associated with a decrease in mortality risk for squamous-cell carcinoma patients (HR = 0.89, 95% CI = 0.82-0.96) and adenocarcinoma patients (HR = 0.87, 95% CI = 0.82-0.94), but not among those with small-cell lung cancer. Post-diagnostic statin exposure was associated with prolonged survival in squamous-cell carcinoma patients (HR = 0.68, 95% CI = 0.59-0.79) and adenocarcinoma patients (HR = 0.78, 95% CI = 0.68-0.89) in a dose-dependent manner.
There is consistent evidence indicating that baseline or post-diagnostic exposure to simvastatin and atorvastatin is associated with extended survival in non-small-cell lung cancer subtypes. These results warrant further randomized clinical trials to evaluate subtype-specific effects of certain statins in patient cohorts with characteristics similar to those examined in this study.
测量不同组织亚型肺癌患者中他汀类药物暴露与死亡率之间的关联。
使用 SEER-Medicare 关联数据库,确定了 19974 名在 2007 年至 2011 年间患有肺癌的个体的队列。分析了诊断前后的他汀类药物暴露情况,以确定与组织亚型分层的患者的癌症特异性死亡率之间的可能关联。采用意向治疗分析和时间依赖性 Cox 回归模型,分别计算诊断前后他汀类药物暴露与死亡率之间的风险比和 95%置信区间(95%CI)。
总体基线他汀类药物暴露与鳞状细胞癌患者(HR=0.89,95%CI=0.82-0.96)和腺癌患者(HR=0.87,95%CI=0.82-0.94)的死亡率降低相关,但与小细胞肺癌患者无关。诊断后他汀类药物暴露与鳞状细胞癌患者(HR=0.68,95%CI=0.59-0.79)和腺癌患者(HR=0.78,95%CI=0.68-0.89)的生存时间延长相关,呈剂量依赖性。
有一致的证据表明,辛伐他汀和阿托伐他汀的基线或诊断后暴露与非小细胞肺癌亚型的生存时间延长有关。这些结果需要进一步的随机临床试验来评估某些他汀类药物在与本研究中检查的患者特征相似的患者队列中的亚型特异性作用。