Department of Respiratory Medicine, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Oncology Center, Gunma University Hospital, Maebashi, Gunma, Japan.
Thorac Cancer. 2022 Nov;13(22):3225-3228. doi: 10.1111/1759-7714.14678. Epub 2022 Oct 4.
Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors are standard therapeutic agents for non-small cell lung cancer (NSCLC) patients with major EGFR mutations such as exon 19 deletions and a L858R mutation, whereas treatment strategies for cases with uncommon EGFR mutations remain to be fully established. Here, we report a long-term (≥20 years from initial diagnosis) NSCLC survivor carrying EGFR L858R and L747V mutations. The patient received gefitinib monotherapy, systemic chemotherapy/chemoimmunotherapy, and local consolidative therapies for oligometastatic lesions, and responded to afatinib rechallenge with a progression-free survival of 12 months. The current case suggests that afatinib is effective in NSCLC patients with EGFR L858R and L747V mutations and that a therapeutic approach combining appropriately timed systemic therapies with local consolidative therapies for oligometastatic lesions improves long-term survival.
表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂是具有主要 EGFR 突变(如外显子 19 缺失和 L858R 突变)的非小细胞肺癌(NSCLC)患者的标准治疗药物,而对于罕见 EGFR 突变的治疗策略仍有待充分确立。在这里,我们报告了一名长期(从初始诊断开始≥20 年)携带 EGFR L858R 和 L747V 突变的 NSCLC 幸存者。该患者接受了吉非替尼单药治疗、系统化疗/化疗免疫治疗以及寡转移病灶的局部巩固治疗,并对阿法替尼进行了重新挑战,无进展生存期为 12 个月。目前的病例表明,阿法替尼对携带 EGFR L858R 和 L747V 突变的 NSCLC 患者有效,并且将适时的系统治疗与寡转移病灶的局部巩固治疗相结合的治疗方法可改善长期生存。