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首页> 外文期刊>Indian journal of cancer. >Clinicopathologic features of non-small cell lung cancer in India and correlation with epidermal growth factor receptor mutational status
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Clinicopathologic features of non-small cell lung cancer in India and correlation with epidermal growth factor receptor mutational status

机译:印度非小细胞肺癌的临床病理特征及其与表皮生长因子受体突变状态的关系

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Introduction: We performed retrospective analysis of 106 patients with lung cancer for which formalin-fixed paraffin-embedded tissues was available. Their epidermal growth factor receptor (EGFR) mutation status and treatment outcomes are described. Materials and Methods: All patients with confirmed non - small cell lung cancer (NSCLC) during Jan 2008 to Dec 2010 were included. EGFR sequencing was performed with ABI PRISM 310 genetic analyzer. Results: Forty-two (39.6%) patients had mutation in one of the four exons characterized. Patients whose EGFR mutational status was not available at presentation before the start of treatment were started on chemotherapy, n = 46 (43.39%). If EGFR mutational analysis was available and mutations were present, the patients were started on either upfront tyrosine kinase inhibitor (TKI), n = 15 (14.15%) or if on chemotherapy arm were allowed to finish six cycles and then start with maintenance TKIs, n = 26 (24.52%). The median progression free survival for patients with and without mutations was 11 months (95% CI,7-14) and 9 months (95% CI,7-10) respectively. A median PFS of 14 months (95%CI, 12-16) was seen in the mutation-positive group that received both chemotherapy followed by switch maintenance with TKIs versus 8 months (95%CI, 7-8 months) in the group that received only TKI. Conclusion: The prevalence of EGFR mutations in this population of NSCLC patients was 39.6% with exon 19 mutation being the most common. The observed benefit of addition of chemotherapy over TKI in EGFR mutation-positive group raises the question, can we offer the therapy of chemotherapy-TKI combination to EGFR mutation-positive lung cancer patients as shown in the present study.
机译:简介:我们对106例可用福尔马林固定石蜡包埋的肺癌患者进行了回顾性分析。描述了它们的表皮生长因子受体(EGFR)突变状态和治疗结果。材料和方法:纳入2008年1月至2010年12月期间所有确诊的非小细胞肺癌(NSCLC)患者。用ABI PRISM 310遗传分析仪进行EGFR测序。结果:四十二例(39.6%)患者的特征是四个外显子之一发生突变。在治疗开始前就诊时尚无EGFR突变状态的患者开始接受化疗,n = 46(43.39%)。如果可以进行EGFR突变分析并且存在突变,则患者可以使用n = 15(14.15%)的预先酪氨酸激酶抑制剂(TKI)开始,或者如果允许在化疗组完成6个周期然后开始维持TKI, n = 26(24.52%)。有突变和无突变的患者的无进展中位生存期分别为11个月(95%CI,7-14)和9个月(95%CI,7-10)。突变阳性组中,接受两种化学疗法后再行TKI维持治疗的患者中位PFS为14个月(95%CI,12-16),而接受TKI的患者则为8个月(95%CI,7-8个月)。仅收到TKI。结论:该NSCLC患者人群中EGFR突变的患病率为39.6%,其中外显子19突变最为常见。 EGFR突变阳性组在化疗中比TKI加化疗有更好的益处,这提出了一个问题,如本研究所示,我们能否为EGFR突变阳性的肺癌患者提供化疗-TKI联合治疗。

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