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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Early neutrophil-to-lymphocyte ratio reduction as a surrogate marker of prognosis in never smokers with advanced lung adenocarcinoma receiving gefitinib or standard chemotherapy as first-line therapy.
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Early neutrophil-to-lymphocyte ratio reduction as a surrogate marker of prognosis in never smokers with advanced lung adenocarcinoma receiving gefitinib or standard chemotherapy as first-line therapy.

机译:在接受吉非替尼或标准化疗作为一线治疗的晚期肺腺癌从未吸烟者中,早期中性粒细胞与淋巴细胞比率的降低是预后的替代指标。

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An inflammatory-immunological marker, neutrophil-to-lymphocyte ratio (NLR), was evaluated as a surrogate indicator for prognosis of advanced lung adenocarcinoma patients.The subjects of this study were 199 never smokers with advanced lung adenocarcinoma, who were enrolled in a prospective randomized phase III study (First-SIGNAL) comparing gefitinib with gemcitabine plus cisplatin as first-line therapy. The values of NLR were assessed at two time points: at baseline (pretreatment) and on day 1 of the second cycle (posttreatment).A higher posttreatment NLR was associated with a worse tumor response (median posttreatment NLR, 1.56 for partial response, 1.64 for stable disease, and 2.70 for progressive disease; P?
机译:炎性免疫标记物中性粒细胞与淋巴细胞的比率(NLR)被评估为晚期肺腺癌患者预后的替代指标。本研究的受试者为199名从不吸烟的晚期肺腺癌患者,他们纳入了前瞻性研究。比较吉非替尼与吉西他滨加顺铂作为一线治疗的随机III期研究(First-SIGNAL)。在两个时间点评估NLR值:基线时(治疗前)和第二个周期的第1天(治疗后)。较高的治疗后NLR与较差的肿瘤反应相关(治疗后中位NLR为1.56,部分反应为1.64稳定疾病为2.70,进行性疾病为2.70; P 0.001)。当治疗后的NLR较高时,进展风险较高[危险比(HR)≥1.23,95%置信区间(CI)1.15-1.31; P≤<0.001]。较高的治疗后NLR会增加死亡风险(HR≥1.13,95%CI 1.06-1.21; P <0.001)。这些关联根据治疗方式没有差异。当根据治疗前和治疗后NLR的临界点将患者分为四组时,与治疗前NLR较高但仍在治疗后仍高的患者相比,治疗前NLR较高而在治疗后明显下降的患者的生存期得到了改善。总体生存率分别为22.0和15.8个月,P 0.001)。治疗后NLR高与预后差有关。有效治疗后NLR的早期降低可能表明预后不良的患者生存率得到了改善。

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