Anhui Provincial Hospital, The First Affiliated Hospital of University of Science and Technology of China, Hefei, Anhui, China (mainland).
Med Sci Monit. 2018 Dec 23;24:9364-9369. doi: 10.12659/MSM.911333.
BACKGROUND Lung cancer has become a leading disease for the tumor-induced mortality. Non-small cell lung cancer (NSCLC) accounts for approximately 80% of all lung cancers. The present research aimed to evaluate the correlation between the anaplastic lymphoma kinase/oncogene or c-ros oncogene 1 (ALK/ROS1) fusions or mutations of epidermal growth factor receptor (EGFR) and ages or gender of patients. MATERIAL AND METHODS Among 1449 NSCLC patients, 457 patients who were diagnosed as consecutive EGFR mutations or ALK/ROS1 fusions between November 2016 and February 2018 were involved in the present study. EGFR genes or ALK/ROS1 mutations were detected by using DNA sequencing technique and amplification-refractory mutation system (ARMS). The mRNAs of ROS1 and ALK fusion were examined by using polymerase chain reaction technique and fusion gene detection kit. RESULTS Females were more often inflicted by the EGFR mutations, especially for the exon 19 deletion and L858R mutation. There were significantly more ALK/ROS1 fusions in females compared to males (P<0.05) and significantly more ALK/ROS1 fusions in <60 years of age patients compared to patients older than 60 years of age (P<0.05). Exon 21 L858R and L861Q dominantly occurred in patients ≥60 years of age and exon 19 deletion in patients <60 years of age. EML-ALK-1 mainly existed in the female NSCLC patients. CONCLUSIONS EGFR mutations and ALK/ROS1 fusions mainly occurred in the NSCLC female patients who were older than 60 years of age.
肺癌已成为肿瘤导致死亡的主要疾病。非小细胞肺癌(NSCLC)约占所有肺癌的 80%。本研究旨在评估间变性淋巴瘤激酶/致癌基因或 c-ros 原癌基因 1(ALK/ROS1)融合或表皮生长因子受体(EGFR)突变与患者年龄或性别之间的相关性。
在 1449 例 NSCLC 患者中,纳入了 457 例于 2016 年 11 月至 2018 年 2 月期间连续诊断为 EGFR 突变或 ALK/ROS1 融合的患者。通过 DNA 测序技术和扩增受阻突变系统(ARMS)检测 EGFR 基因或 ALK/ROS1 突变。通过聚合酶链反应技术和融合基因检测试剂盒检测 ROS1 和 ALK 融合的 mRNAs。
女性更常发生 EGFR 突变,尤其是外显子 19 缺失和 L858R 突变。与男性相比,女性中 ALK/ROS1 融合的发生率显著更高(P<0.05),且<60 岁患者中 ALK/ROS1 融合的发生率显著高于>60 岁患者(P<0.05)。外显子 21 的 L858R 和 L861Q 突变主要发生在年龄≥60 岁的患者中,外显子 19 缺失主要发生在年龄<60 岁的患者中。EML-ALK-1 主要存在于女性 NSCLC 患者中。
EGFR 突变和 ALK/ROS1 融合主要发生在年龄>60 岁的老年 NSCLC 女性患者中。