Effects of EGFR Mutations on NSCLC Patients Treated by Ramucirumab plus Docetaxel

IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY
Hua Gong
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Abstract

The present paper attempted to define the effects of epidermal growth factor receptor (EGFR) mutations on patients with non-small cell lung cancer (NSCLC) treated by ramucirumab plus docetaxel. Of the 82 enrolled patients, 48 underwent EGFR mutations, showing relevance to sex and smoking history (P<0.05). The analysis yielded that EGFR-mutant (EGFR-Mut) group had a higher objective response rate versus EGFR-wild-type (EGFR-Wt) group (P<0.05). Subsequent to treatment, serum VEGF, bFGF, HDGF, CEA, CA153, CYFRA21-1 and CA199 levels dropped more significantly in EGFR-Mut group (P<0.05). Beyond that, EGFR-Mut exhibited a lower ZPS score and a higher KPS score versus EGFR-Wt group (P<0.05). Further, EGFR-Mut patients displayed strikingly longer median survival time versus EGFR-Wt patients (P<0.05). Ramucirumab plus docetaxel can safely inhibit tumour angiogenesis and regulate the levels of serum tumour markers. EGFR-Mut NSCLC patients with brain metastasis have better treatment outcomes and longer survival.
EGFR突变对Ramucirumab联合多西他赛治疗NSCLC患者的影响
本文试图确定表皮生长因子受体(EGFR)突变对ramucirumab联合多西他赛治疗的非小细胞肺癌(NSCLC)患者的影响。在82例入组患者中,48例发生EGFR突变,与性别和吸烟史相关(P<0.05)。分析结果显示,egfr突变型(EGFR-Mut)组的客观有效率高于egfr野生型(EGFR-Wt)组(P<0.05)。治疗后,EGFR-Mut组患者血清VEGF、bFGF、HDGF、CEA、CA153、CYFRA21-1、CA199水平下降更为显著(P<0.05)。除此之外,EGFR-Mut组ZPS评分较EGFR-Wt组低,KPS评分较高(P<0.05)。此外,EGFR-Mut患者的中位生存时间明显长于EGFR-Wt患者(P<0.05)。Ramucirumab联合多西他赛可以安全地抑制肿瘤血管生成并调节血清肿瘤标志物的水平。EGFR-Mut NSCLC脑转移患者治疗效果更好,生存期更长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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