Zhu Ying, Fu Lei, Jing Wang, Kong Li, Yu Jinming
Department of Clinical Medicine, Weifang Medical University, Weifang, Shandong Province, People's Republic of China.
Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Jinan, People's Republic of China.
Cancer Manag Res. 2019 Dec 31;11:10901-10908. doi: 10.2147/CMAR.S197245. eCollection 2019.
Adjuvant radiotherapy in non-small-cell lung cancer (NSCLC) remains controversial,Whether the mutation status of epidermal growth factor receptor (EGFR) will affect the recurrence and survival of patients with resected NSCLC is rarely reported. Our purpose is to study the effect of postoperative radiotherapy on patients with stage IIIA(N2) NSCLC with EGFR mutation.
Total of of 115 patients diagnosed with stage IIIA(N2) resected NSCLC were analyzed retrospectively. Their EGFR mutations were detected by real-time quantitative PCR and DNA sequencing technology together.
At a median follow-up of 34.2 months for the postoperative adjuvant radiotherapy (PORT) group and 31.0 months for the non-PORT group, PORT group significantly improved progression free survival (PFS) and overall survival (OS). The median PFS and OS in the EGFR mutant group were not significantly longer than those in the EGFR wild-type group. The number of chemotherapy cycles, postoperative radiotherapy and the number of metastatic lymph nodes were independent factors influencing long-term survival.
Our retrospective analysis showed that PORT can improve survival of patients with stage IIIA(N2) NSCLC. EGFR-mutant group with stage IIIA(N2) NSCLC has a tendency of a higher survival than the wild-type EGFR group, but there was no significant difference for both groups. The EGFR mutation status was not associated with PFS or OS of stage IIIA(N2) NSCLC.
非小细胞肺癌(NSCLC)的辅助放疗仍存在争议,表皮生长因子受体(EGFR)的突变状态是否会影响接受手术切除的NSCLC患者的复发和生存情况鲜有报道。我们的目的是研究术后放疗对伴有EGFR突变的IIIA期(N2)NSCLC患者的影响。
回顾性分析115例确诊为IIIA期(N2)且接受手术切除的NSCLC患者。同时采用实时定量PCR和DNA测序技术检测他们的EGFR突变情况。
术后辅助放疗(PORT)组的中位随访时间为34.2个月,非PORT组为31.0个月,PORT组显著改善了无进展生存期(PFS)和总生存期(OS)。EGFR突变组的中位PFS和OS并不显著长于EGFR野生型组。化疗周期数、术后放疗以及转移淋巴结数量是影响长期生存的独立因素。
我们的回顾性分析表明,PORT可提高IIIA期(N2)NSCLC患者的生存率。伴有EGFR突变的IIIA期(N2)NSCLC组比EGFR野生型组有更高的生存倾向,但两组之间无显著差异。EGFR突变状态与IIIA期(N2)NSCLC的PFS或OS无关。