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EGFR mutations in patients with non-small cell lung cancer from mainland China and their relationships with clinicopathological features: a meta-analysis

机译:中国大陆非小细胞肺癌患者EGFR基因突变及其与临床病理特征的关系:荟萃分析

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Many studies have reported the EGFR mutations in Chinese non small cell lung cancer (NSCLC) patients and their relationship with clinicopathological characteristics. But the frequency and type of EGFR mutations are varied. The relationship between EGFR mutations and clinicopathological characteristics remains unclear. We systematically reviewed studies of EGFR mutations in mainland Chinese NSCLC patients. Standard statistical methods for meta-analysis were applied. A total of 5,442 patients from 21 studies were included in the meta-analysis. The overall EGFR mutation rate was 37.5% (2,039/5,442). Among those 1,935 patients with detailed data about EGFR mutation types, the most prevalent mutation type was L858R, which accounted for 38.3% of all EGFR mutations. EGFR-TKIs sensitive mutations occupied 88.5% of all EGFR mutations. While the acquired EGFR-TKIs resistant mutations (T790 M) could occur naturally at the frequency of 1.5% without exposure of EGFR-TKIs. Male patients had a lower mutation rate than female patients (32.6% versus 53.0%, OR=0.40, 95% CI: 0.34-0.48, emP/em < 0.001). The EGFR mutation rate for smokers was 19.2%, lower than that for non-smokers (47.9%) (OR = 0.40, 95% CI: 0.34-0.48, emP/em < 0.001). Patients with adenocarcinoma had a higher mutation rate than those with non-adenocarcinoma (50.2% versus 17.0%, OR = 4.84, 95% CI: 4.07-5.75, emP/em < 0.001). EGFR mutation rate did not differ significantly between stage I and stage II/III/IV patients (35.8% versus 32.2%, OR = 1.08, 95% CI: 0.84-1.43, emP/em = 0.580). Our results show that EGFR mutation rate is high in mainland Chinese NSCLC patients. EGFR-TKIs sensitive mutations are main types of mutations. EGFR mutations are significantly associated with gender, smoking history, histology type, but not stage.
机译:许多研究报告了中国非小细胞肺癌(NSCLC)患者的EGFR突变及其与临床病理特征的关系。但是EGFR突变的频率和类型各不相同。 EGFR突变与临床病理特征之间的关系尚不清楚。我们系统地回顾了中国大陆非小细胞肺癌患者中EGFR突变的研究。应用荟萃分析的标准统计方法。荟萃分析包括来自21项研究的5,442例患者。总体EGFR突变率为37.5%(2,039 / 5,442)。在这1935名具有EGFR突变类型详细数据的患者中,最普遍的突变类型是L858R,占所有EGFR突变的38.3%。 EGFR-TKIs敏感突变占所有EGFR突变的88.5%。尽管获得的EGFR-TKIs抗性突变(T790 M)可以以1.5%的频率自然发生而无需暴露EGFR-TKIs。男性患者的突变率低于女性患者(32.6%对53.0%,OR = 0.40,95%CI:0.34-0.48, P < 0.001)。吸烟者的EGFR突变率为19.2%,低于非吸烟者的EGFR突变率为47.9%(OR = 0.40,95%CI:0.34-0.48, P < 0.001)。腺癌患者的突变率高于非腺癌患者(50.2%比17.0%,OR = 4.84,95%CI:4.07-5.75, P < 0.001)。 I期和II / III / IV期患者的EGFR突变率无显着差异(35.8%比32.2%,OR = 1.08,95%CI:0.84-1.43, P = 0.580)。我们的结果表明,中国大陆非小细胞肺癌患者的EGFR突变率很高。 EGFR-TKIs敏感突变是突变的主要类型。 EGFR突变与性别,吸烟史,组织学类型显着相关,但与阶段无关。

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