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首页> 外文期刊>Clinical lung cancer >Assessment of folate receptor-α and epidermal growth factor receptor expression in pemetrexed-treated non-small-cell lung cancer patients
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Assessment of folate receptor-α and epidermal growth factor receptor expression in pemetrexed-treated non-small-cell lung cancer patients

机译:培美曲塞治疗的非小细胞肺癌患者叶酸受体-α和表皮生长因子受体表达的评估

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摘要

Introduction Folate receptor-α regulates cellular uptake of folates and antifolates (eg, pemetrexed) and is frequently expressed in pulmonary adenocarcinoma. EGFR is an established therapeutic target in NSCLC. Therapies targeting FRA or EGFR are available. The association between FRA and EGFR expression in advanced NSCLC has not been explored. Combining therapeutic FRA antibodies with an EGFR inhibitor might be beneficial, if both of the targets are significantly coexpressed.Patients and Methods Specimens from 160 advanced NSCLC patients receiving pemetrexed-based chemotherapy were assessed for membranous FRA and EGFR protein expression using immunohistochemistry and the Hybrid (H)-score. EGFR (exons 18-21) and Kirsten RNA-associated rat sarcoma 2 virus (exon 2) mutations were determined.Results were correlated to patients' clinicopathological data, progression-free survival (PFS), and overall survival (OS). Results Forty-seven patients (29%) had tumors with strong FRA and EGFR expression, but no statistically significant correlation was seen between protein levels of FRA and EGFR. High membranous FRA expression (H-score ≥20) was associated with prolonged PFS (5.5 vs. 3.4 months; hazard ratio [HR], 0.6060; P =.0254) and improved OS (12.1 vs. 6.4 months; HR, 0.5726; P =.0076).Conclusion Survival times are improved in NSCLC patients whose tumors show strong membranous FRA expression. No statistical correlation between membranous FRA and EGFR expression was demonstrated in advanced NSCLC, but 47 patients (29%) had higher expression of both of the receptors and could be suitable for combined targeted therapies.
机译:简介叶酸受体α调节细胞摄取叶酸和抗叶酸(例如,培美曲塞),并经常在肺腺癌中表达。 EGFR是NSCLC中已确立的治疗靶标。有针对FRA或EGFR的疗法。尚未探讨晚期非小细胞肺癌中FRA和EGFR表达之间的关联。如果两个靶标均显着共表达,则将治疗性FRA抗体与EGFR抑制剂结合可能是有益的。 H)分。确定EGFR(外显子18-21)和与Kirsten RNA相关的大鼠肉瘤2病毒(外显子2)突变,并将结果与​​患者的临床病理数据,无进展生存期(PFS)和总体生存期(OS)相关。结果47例患者(29%)的肿瘤中FRA和EGFR表达强,但FRA和EGFR蛋白水平之间无统计学意义。膜性FRA高表达(H评分≥20)与PFS延长(5.5 vs. 3.4个月;危险比[HR],0.6060; P = .0254)和OS改善(12.1 vs. 6.4个月; HR,0.5726; P <0.05)相关。 P = .0076)。结论在肿瘤表现出强烈的膜状FRA表达的NSCLC患者中,生存时间得到了改善。在晚期NSCLC中未发现膜性FRA与EGFR表达之间的统计相关性,但47例患者(29%)的两种受体均具有较高的表达,可能适合联合靶向治疗。

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