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EGFR-TKI一线治疗不同EGFR突变状态晚期非小细胞肺癌疗效分析
引用本文:姜海英,李艳芳,朱梅,李倩,吕姣. EGFR-TKI一线治疗不同EGFR突变状态晚期非小细胞肺癌疗效分析[J]. 国际肿瘤学杂志, 2017, 44(1). DOI: 10.3760/cma.j.issn.1673-422X.2017.01.005
作者姓名:姜海英  李艳芳  朱梅  李倩  吕姣
作者单位:221005,徐州市肿瘤医院肿瘤内科
基金项目:国家十二五科技支撑计划
摘    要:目的:分析表皮生长因子受体酪氨酸酶抑制剂(EGFR-TKI)一线治疗不同EGFR突变状态(外显子19缺失、21突变)晚期非小细胞肺癌(NSCLC)的疗效。方法收集徐州市肿瘤医院经组织病理学证实的EGFR突变阳性晚期NSCLC患者72例,分析两种不同EGFR突变状态与一线EGFR-TKI治疗的客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)以及总生存期(OS)之间的关系。结果72例患者均进行EGFR基因检测,其中37例为EGFR19外显子缺失,35例为EGFR21外显子突变。72例患者均可评价疗效,其中EGFR19外显子缺失的患者ORR 75.7%,DCR 89.2%;EGFR21外显子突变的患者ORR 51.4%,DCR 68.6%,差异均有统计学意义(χ2=4.583,P=0.032;χ2=4.636,P=0.031)。EGFR19外显子缺失和21外显子突变的患者校正后的中位PFS分别为13.2个月、10.8个月,差异有统计学意义(χ2=4.700,P=0.030);中位OS分别为30.2个月、25.6个月,差异有统计学意义(χ2=4.686,P=0.030)。两组间不良反应无明显差别,皮疹最为常见,两组差异无统计学意义(48.7%∶48.6%,χ2=0.000,P=0.995)。结论 EGFR突变状态是晚期NSCLC患者一线EGFR-TKI治疗疗效和OS的预测因素,EGFR19外显子缺失患者的疗效优于EGFR21外显子突变患者。

关 键 词:受体,表皮生长因子  癌,非小细胞肺  表皮生长因子受体酪氨酸酶抑制剂

Association between EGFR mutation status and efficacy of first-line EGFR-TKI in patients with ;advanced non-small cell lung cancer
Jiang Haiying,Li Yanfang,Zhu Mei,Li Qian,Lyu Jiao. Association between EGFR mutation status and efficacy of first-line EGFR-TKI in patients with ;advanced non-small cell lung cancer[J]. Journal of International Oncology, 2017, 44(1). DOI: 10.3760/cma.j.issn.1673-422X.2017.01.005
Authors:Jiang Haiying  Li Yanfang  Zhu Mei  Li Qian  Lyu Jiao
Abstract:Objective To evaluated the effect of first-line epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI)on advanced non-small cell lung cancer (NSCLC)patients with different EGFR mutation status (exon 1 9 deletion and exon 21 mutation).Methods Seventy-two advanced NSCLC patients with EGFR mutation confirmed by histopathology were enrolled.All of the patients received first-line EGFR-TKI.The relationships between EGFR mutation status and objective response rate (ORR),disease control rate (DCR),progression free survival (PFS ) and overall survival (OS ) were analyzed.Results Of the 72 patients,37 patients expressed exon 1 9 deletion,35 patients expressed exon 21 mutation,and all of them could be evaluated.The ORR and DCR of patients with exon 1 9 deletion were higher than those of patients with exon 21 mutation (75.7%vs.51 .4%,χ2 =4.583,P=0.032;89.2%vs.68.6%,χ2 =4.636,P=0.031 ).The modified median PFS of patients with exon 1 9 deletion was significantly higher than that of patients with exon 21 mutation (1 3.2 month vs.1 0.8 month,χ2 =4.700,P=0.030).The median OS of patients with exon 1 9 deletion was significantly higher than that of patients with exon 21 mutation (30.2 month vs.25.6 month,χ2 =4.686,P=0.030).The side effects were similar between the two groups.The most common adverse reaction was rash,and the incidence had no significant difference between the two groups (48.7% vs.48.6%,χ2 =0.000,P=0.995 ).Conclusion EGFR mutation status is a predictor for PFS,OS and ORR of first-line EGFR-TKI in patients with advanced NSCLC.NSCLC patients with EGFR exon 1 9 deletion are associated with longer survival time and better response rate compared with those with exon 21 mutation.
Keywords:Receptor,epidermal growth factor  Carcinoma,non-small-cell lung  EGFR-TKI
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