...
首页> 外文期刊>Thoracic cancer. >Epidermal growth factor receptor‐tyrosine kinase inhibitor therapy is especially beneficial to patients with exon 19 deletion compared with exon 21 L858R mutation in non‐small‐cell lung cancer: Systematic review and meta analysis
【24h】

Epidermal growth factor receptor‐tyrosine kinase inhibitor therapy is especially beneficial to patients with exon 19 deletion compared with exon 21 L858R mutation in non‐small‐cell lung cancer: Systematic review and meta analysis

机译:与非小细胞肺癌中外显子21 L858R突变相比,表皮生长因子受体酪氨酸激酶抑制剂治疗特别有利于外显子19缺失的患者:系统评价和荟萃分析

获取原文

摘要

Background The correlation between epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) and EGFR sensitive mutation subtypes in advanced or metastatic non-small cell lung cancer (NSCLC) remains uncertain. We performed this meta-analysis to determine different clinical outcomes between patients with exon 19 deletion accepting EGFR-TKI therapy compared with those with exon 21 L858R mutation. Methods PubMed and Web of Science were analyzed for eligible trials. Raw data were extracted to give pooled estimates of the effect of EGFR-TKI therapy on objective response rate (ORR), one-year progression-free survival (PFS), and two-year overall survival (OS). Results We identified 13 eligible trials involving 912 patients. Prospective meta-analysis demonstrated that the ORR of the 19 deletion group was significantly higher than the 21 L858R mutation group (odds ratio [OR] 1.98, 95% confidence interval [CI] 1.18–3.33; P = 0.01), but no statistical significance between the one-year PFS rate of the 19 deletion and 21 L858R groups (OR 1.44, 95% CI 0.96–2.18; P = 0.08) was found. However, retrospective meta-analysis demonstrated that a significantly higher one-year PFS rate was associated with the 19 deletion group (OR 1.73, 95% CI 1.17–2.56; P = 0.006). The two-year survival rate of the 19 deletion group was significantly higher than the 21 L858R group (OR 5.27, 95 % CI 1.76–15.71; P = 0.003). Conclusions In advanced NSCLC patients, an exon 19 deleton may provide superior ORR, PFS, and OS after EGFR-TKI treatment compared with an exon 21 L858R mutation.
机译:背景技术在晚期或转移性非小细胞肺癌(NSCLC)中,表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)与EGFR敏感突变亚型之间的相关性仍不确定。我们进行了这项荟萃分析,以确定在接受EGFR-TKI治疗的外显子19缺失患者与外显子21 L858R突变患者之间不同的临床结果。方法对PubMed和Web of Science进行分析以进行合格试验。提取原始数据以汇总评估EGFR-TKI治疗对客观缓解率(ORR),一年无进展生存期(PFS)和两年总体生存期(OS)的影响。结果我们确定了13项合格试验,涉及912名患者。前瞻性荟萃分析表明,19个缺失组的ORR显着高于21个L858R突变组(几率[OR] 1.98,95%置信区间[CI] 1.18–3.33; P = 0.01),但无统计学意义。在19个缺失组和21个L858R组的一年PFS率之间(OR 1.44,95%CI 0.96-2.18; P = 0.08)被发现。但是,回顾性荟萃分析表明,与19个缺失组相关的一年PFS率明显更高(OR 1.73,95%CI 1.17-2.56; P = 0.006)。 19个缺失组的两年生存率显着高于21个L858R组(OR 5.27,95%CI 1.76-15.71; P = 0.003)。结论在晚期NSCLC患者中,与外显子21 L858R突变相比,外显子19 deleton在EGFR-TKI治疗后可提供更好的ORR,PFS和OS。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号