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首页> 外文期刊>Asia-Pacific journal of clinical oncology >The value of blood biomarkers of progression and prognosis in ALK‐positive patients with non–small cell lung cancer treated with crizotinib
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The value of blood biomarkers of progression and prognosis in ALK‐positive patients with non–small cell lung cancer treated with crizotinib

机译:用克里齐替尼治疗的非小细胞肺癌的ALK阳性患者血液生物标志物的价值

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Abstract Aim Valuable and convenient prognostic predictors are essential for targeted therapy of non–small cell lung cancer (NSCLC). Patients with early‐stage cancer and EGFR mutations who's neutrophils‐to‐lymphocytes rate (NLR) could be prognostic factor to evaluate efficacy. However, the prognostic role of NLR in patients receiving ALK inhibitors has not been established. Additionally, the relation between the efficacy of ALK inhibitors and derived NLR (dNLR), platelets‐to‐lymphocytes rate (PLR), white blood cells (WBC) and hemoglobin (HGB) are still unknown. Methods This is a retrospective single‐center study and enrolled 113 staged IIIB–IV ALK‐positive NSCLC patients who had received crizotinib treatment. Pretreatment NLR, dNLR, PLR, WBC, HGB were collected and calculated. Cox regression analysis were conducted to study the prognostic roles of NLR, dNLR, PLR, WBC, and HGB on progression‐free survival (PFS) and overall survival (OS). Z ‐test was utilized to identify the difference among all predictive factors’ receiver‐operating characteristics (ROC) curves. Results The median PFS and OS were 10.1 and 23.4 months. Elevated NLR, dNLR, PLR and decreased HGB were associated with worse PFS (95% confidence interval [CI], 1.078–2.304, P ?=?0.018; 95% CI, 1.043–2.222, P ?=?0.028; 95% CI, 1.257–2.757, P ?=?0.002; 95% CI, 0.368–0.843, P ?=?0.005, respectively) and OS (95% CI, 1.698–5.721, P ??0.001; 95% CI, 1.273–3.984, P ?=?0.005; 95% CI, 2.174–6.347, P ??0.001; 95% CI, 0.246–0.710, P ?=?0.001, respectively). Z ‐test revealed there were no significant differences between single factors or combination of them to predict the efficacy. Conclusions Trend of NLR, dNLR, PLR and WBC could be used to identify patients progress status in ALK‐positive NSCLC patients receiving crizotinib. Combination of all biomarkers is no superior to single biomarker.
机译:摘要目标有价值,方便的预测预测因子对于非小细胞肺癌(NSCLC)的靶向治疗至关重要。患有早期癌症和EGFR突变的患者是评估疗效的预后因素。然而,NLR在接受ALK抑制剂的患者中的预后作用尚未建立。另外,ALK抑制剂和衍生NLR(DNLR),血小板到淋巴细胞率(PLR),白细胞(WBC)和血红蛋白(HGB)之间的关系仍然未知。方法这是回顾性单中心研究,并注册了113例患有屈服治疗的IIIB-IV ALK阳性NSCLC患者。收集和计算预处理NLR,DNLR,PLR,WBC,HGB。进行COX回归分析,研究NLR,DNLR,PLR,WBC和HGB对无进展存活(PFS)和总存活(OS)的预后作用。利用Z -Test用于识别所有预测因素的接收器操作特征(ROC)曲线之间的差异。结果中位数和OS为10.1和23.4个月。升高的NLR,DNLR,PLR和HGB减少与更差的PFS相关(95%置信区间[CI],1.078-2.304,P?= 0.018; 95%CI,1.043-2.222,P?= 0.028; 95%CI ,1.257-2.757,p?= 0.002; 95%CI,0.368-0.843,p?= 0.005分别)和OS(95%CI,1.698-5.721,P≤0.001; 0.273 -3.984,p?= 0.005; 95%CI,2.174-6.347,p≤x≤0.001; 95%CI,0.246-0.710,p?= 0.001分别)。 Z -Test透露,单一因素或它们的组合之间没有显着差异来预测疗效。结论NLR,DNLR,PLR和WBC的趋势可用于鉴定接受屈曲in的ALK阳性NSCLC患者的患者进展状态。所有生物标志物的组合不优于单一生物标志物。

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