首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Changes in plasma mass-spectral profile in course of treatment of non-small cell lung cancer patients with epidermal growth factor receptor tyrosine kinase inhibitors.
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Changes in plasma mass-spectral profile in course of treatment of non-small cell lung cancer patients with epidermal growth factor receptor tyrosine kinase inhibitors.

机译:表皮生长因子受体酪氨酸激酶抑制剂的非小细胞肺癌患者治疗非小细胞肺癌患者等离子体质谱谱的变化。

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INTRODUCTION: Our previous study showed that pretreatment serum or plasma Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry may predict clinical outcome of non-small cell lung cancer (NSCLC) patients treated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). In this study, plasma proteomic profiles of NSCLC patients were evaluated in the course of EGFR TKIs therapy. MATERIALS AND METHODS: Plasma samples were collected at baseline, in the course of gefitinib therapy and at treatment withdrawal. Samples were analyzed by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry. Acquired spectra were classified by the VeriStrat test into "good" and "poor" profiles. The association between VeriStrat classification and progression-free survival (PFS) and overall survival (OS), and types of clinical progression, was analyzed. RESULTS: Plasma samples from 111 NSCLC patients treated with gefitinib were processed. VeriStrat "good" classification at baseline correlated with longer PFS (hazard ratio [HR], 0.54; 95% confidence interval, 0.35-0.83; p = 0.005) and OS (HR, 0.40; 95% confidence interval, 0.26-0.61; p < 0.0001), when compared with VeriStrat "poor." Multivariate analysis confirmed longer PFS (HR, 0.52; p = 0.025) and OS (HR, 0.44; p = 0.001) in patients classified as VeriStrat "good", when VeriStrat was considered as a time-dependent variable. About one-third of baseline "good" classifications had changed to "poor" at the time of treatment withdrawal; progression in these patients was associated with the development of new lesions. CONCLUSIONS: Our findings support the role of VeriStrat in the assistance in treatment selection of NSCLC patients for EGFR TKI therapy and its potential utility in treatment monitoring.
机译:介绍:我们以前的研究表明,预处理血清或血浆基质辅助激光解吸/电离飞行时间质谱仪可以预测与表皮生长因子受体(EGFR)酪氨酸处理的非小细胞肺癌(NSCLC)患者的临床结果激酶抑制剂(TKI)。在本研究中,在EGFR TKIS治疗过程中评估了NSCLC患者的血浆蛋白质组学谱。材料和方法:在基线中收集血浆样品,在吉非替尼治疗和治疗戒断过程中。通过基质辅助激光解吸/电离飞行时间质谱法分析样品。获得的光谱被Veristrat测试分类为“好”和“差”配置文件。分析了Veristrat分类和无进展存活(PFS)和整体存活(OS)以及临床进展的关联。结果:加工111例NSCLC患者的血浆样品,处理了吉替尼治疗的患者。 Veristrat在基线上分类与较长的PFS相关(危险比[HR],0.54; 95%置信区间,0.35-0.83; p = 0.005)和OS(HR,0.40; 95%置信区间,0.26-0.61; p <0.0001),与Veristrat相比“穷人”。当Veristrat被认为是时间相关的变量时,多变量分析确认了较长的PFS(HR,0.52; p = 0.025)和OS(HR,0.44; p = 0.001),veristrat“好”时,veristrat“好”。大约三分之一的基线“良好”分类在治疗时已经改为“贫困”退出;这些患者的进展与新病变的发展有关。结论:我们的调查结果支持Veristrat在EGFR TKI治疗的NSCLC患者治疗选择中的援助中的作用及其在治疗监测中的潜在效用。

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