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Survival and prognostic factors in non-small cell lung cancer patients with mutation of the EGFR gene treated with tyrosine kinase inhibitors in a peruvian hospital

机译:在秘鲁医院用酪氨酸激酶抑制剂治疗的EGFR基因突变的非小细胞肺癌患者的生存和预后因素

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The identification of the epidermal growth factor mutation (EGFR) is a positive prognostic factor for survival and therapeutic response to tyrosine kinase inhibitors (TKIs) in patients with non-small cell lung cancer (NSCLC). TKIs are considered first line treatment in Patients with stages IIIB and IV NSCLC. We investigated the survival and prognostic factors in NSCLC patients with the mutation of the EGFR in routine clinical practice. We conducted a retrospective cohort observational study of 72 patients with non-small cell lung cancer (NSCLC) with EGFR gene mutations that received treatment with erlotinib from January 2009 to December 2015. Kaplan-Meier curves were presented. The association between independent variables and survival was analyzed using the Long-Rank test in bivariate analysis and for multivariate analysis, Cox proportional hazards method was used to calculate hazard ratios (HRs) and corresponding 95% confidence intervals (CIs). We included data from 72 patients, which were followed for a total of 1144 patient-months. The majority of patients were female (61.11%), non-smokers (62.50%), and with histological type corresponding to adenocarcinoma (76.38%). The most frequent EGFR gene mutation was the deletion of exon 19 (65.27%). The majority of patients presented with comorbidities (77.78%), most commonly hypertension. Almost all patients had stage IV NSCLC. Out of the 72 cases, 65 (90.28%) died. The median survival was 9.3 months (95% CI, 7.01-16.93). When comparing the survival curves when using the Log Rank Test, histological type (P = 0.01), place of mutation (P = 0.06), hemoglobin (P = 0.01) and age (P = 0.01) were significant associated to overall survival (OS). In multivariate analysis, only age (HR, 1.02; 95% CI, 1-1.04, P = 0.009) and hemoglobin (HR, 0.70; 95% CI, 0.55-0.89, P = 0.003) remained significant. In conclusion, the median OS of NSCLC patients with positive EGFR gene mutation treated with TKI was 9.3 months. Bivariate and multivariate analysis showed that younger age and a higher hemoglobin level were the most important factors associated with survival.
机译:表皮生长因子突变(EGFR)的鉴定是非小细胞肺癌(NSCLC)患者生存和对酪氨酸激酶抑制剂(TKIs)的治疗反应的阳性预后因素。对于患有IIIB和IV期NSCLC的患者,TKI被视为一线治疗。在常规临床实践中,我们调查了EGFR突变的NSCLC患者的生存和预后因素。我们对2009年1月至2015年12月接受erlotinib治疗的72例具有EGFR基因突变的非小细胞肺癌(NSCLC)患者进行了一项回顾性队列研究。显示了Kaplan-Meier曲线。在双变量分析中使用Long-Rank检验分析了独立变量与生存之间的关联,对于多变量分析,使用Cox比例风险法计算风险比(HRs)和相应的95%置信区间(CIs)。我们纳入了来自72位患者的数据,总共随访了1144个患者-月。大多数患者为女性(61.11%),不吸烟者(62.50%),并且组织学类型与腺癌相对应(76.38%)。最常见的EGFR基因突变是第19外显子的缺失(65.27%)。大多数患者出现合并症(77.78%),最常见的是高血压。几乎所有患者均患有IV期NSCLC。在72例中,有65例(90.28%)死亡。中位生存期为9.3个月(95%CI,7.01-16.93)。使用Log Rank检验比较生存曲线时,组织学类型(P = 0.01),突变位点(P = 0.06),血红蛋白(P = 0.01)和年龄(P = 0.01)与总体生存率(OS)显着相关)。在多变量分析中,只有年龄(HR,1.02; 95%CI,1-1.04,P = 0.009)和血红蛋白(HR,0.70; 95%CI,0.55-0.89,P = 0.003)仍然显着。总之,用TKI治疗的EGFR基因突变阳性的NSCLC患者的中位OS为9.3个月。双因素和多因素分析表明,年龄较小和血红蛋白水平较高是与生存有关的最重要因素。

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