Fang Yu-Hung, Yang Yao-Hsu, Hsieh Meng-Jer, Hung Ming-Szu, Lin Yu-Ching
Division of Thoracic Oncology, Department of Pulmonary and Critical Care Medicine, Chang Gung Memorial Hospital, Chiayi Branch, Puzi City, Chiayi County, Taiwan, R.O.C.
Department of Traditional Chinese Medicine, Chang Gung Memorial Hospital, Chiayi Branch, Puzi City, Chiayi County, Taiwan, R.O.C.
Cancer Manag Res. 2019 Sep 19;11:8539-8546. doi: 10.2147/CMAR.S222278. eCollection 2019.
Concurrent proton pump inhibitor (PPI) use might reduce the plasma concentration of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs). Clinically, the adverse effect of PPIs on patients with non-small cell lung cancer (NSCLC) treated with first-line EGFR TKIs remains controversial. This study was conducted to evaluate whether the combined use of gefitinib with PPIs affected NSCLC outcomes.
We performed a nationwide cohort study of patients newly diagnosed with NSCLC between 1997 and 2013 using the Taiwan Cancer Registry and Taiwan National Health Insurance databases. We identified patients who were treated with first-line EGFR TKIs and analyzed the association between use of PPIs and TKI treatment outcome. We defined the coverage ratio of PPIs as duration of PPI treatment in days divided by duration of TKIs in days. Patients who exhibited an overlap of >20% between PPI and TKI usage days were defined as having a high coverage ratio.
A total of 1278 patients were treated with first-line gefitinib, 309 of which took PPIs at the same time and 145 had a high PPI coverage ratio. Patients had similar time to failure regardless of their PPI coverage ratio during gefitinib treatment. However, higher PPI coverage ratio significantly decreased overall survival (OS) compared with that of patients with a lower PPI coverage ratio or no PPI treatment in univariate analysis (median OS, 13.5, 16.7, and 21.8 months, respectively, <0.01) and multivariate analyses (high coverage ratio HR: 1.67; low coverage ratio HR: 1.29). Exposure to PPIs during first line gefitinib treatment significantly decreased overall survival of patients with NSCLC.
Concurrent use of PPIs was associated with lower overall survival in patients with EGFR-mutant NSCLC under first-line gefitinib treatment.
同时使用质子泵抑制剂(PPI)可能会降低表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)的血浆浓度。临床上,PPI对一线EGFR-TKIs治疗的非小细胞肺癌(NSCLC)患者的不良影响仍存在争议。本研究旨在评估吉非替尼与PPI联合使用是否会影响NSCLC的治疗结果。
我们利用台湾癌症登记处和台湾全民健康保险数据库,对1997年至2013年间新诊断为NSCLC的患者进行了一项全国性队列研究。我们确定了接受一线EGFR-TKIs治疗的患者,并分析了PPI使用与TKI治疗结果之间的关联。我们将PPI的覆盖比例定义为PPI治疗天数除以TKI治疗天数。PPI和TKI使用天数重叠>20%的患者被定义为高覆盖比例。
共有1278例患者接受一线吉非替尼治疗,其中309例同时服用PPI,145例PPI覆盖比例高。在吉非替尼治疗期间,无论PPI覆盖比例如何,患者的无进展生存期相似。然而,在单因素分析中,与低PPI覆盖比例或未接受PPI治疗的患者相比,高PPI覆盖比例显著降低了总生存期(OS)(中位OS分别为13.5、16.7和21.8个月,P<0.01),在多因素分析中也是如此(高覆盖比例HR:1.67;低覆盖比例HR:1.29)。一线吉非替尼治疗期间使用PPI显著降低了NSCLC患者的总生存期。
在一线吉非替尼治疗下,EGFR突变的NSCLC患者同时使用PPI与较低的总生存期相关。