Ma Chunhua, Liu Mei, Mu Ning, Li Jinduo, Li Lin, Jiang Rong
Department of Intervention, Tianjin HuanHu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Diseases, Tianjin, China.
Medicine (Baltimore). 2020 Oct 23;99(43):e22851. doi: 10.1097/MD.0000000000022851.
Liquid biopsy of cerebrospinal fluid (CSF) and sequencing of cell-free DNA has rarely been used to identify epidermal growth factor receptor (EGFR) mutations, which can guide the design of precise, personalized treatment for patients with leptomeningeal metastasis from lung adenocarcinoma.
A 42-year-old woman with lung adenocarcinoma and leptomeningeal metastasis was admitted to our hospital on March 31, 2019. She exhibited no response to treatment with gefitinib, osimertinib, or chemoradiotherapy and was in critical condition, with an expected survival of <4 weeks.
Next-generation sequencing of CSF and peripheral blood samples identified an EGFR complex mutation (exon19del+K754E).
On April 10, 2019, the patient started oral afatinib (40 mg po qd), but she developed a grade III oral mucosal reaction 1 week later. The afatinib dose was reduced to 30 mg po qd.
At the follow-up examination on May 15, 2019, the patient reported relief from headaches. Enhanced magnetic resonance imaging revealed a reduction in abnormal leptomeningeal enhancement, and the CSF pressure and carcinoembryonic antigen levels were also reduced. The patient continued to respond to afatinib treatment (30 mg once daily) with minimal adverse effects.
This is the first case report of clinical improvement after afatinib treatment in a patient with lung adenocarcinoma and leptomeningeal metastasis harboring an EGFR complex mutation (exon19del+K754E), and thus provides a clinical reference for treatment with afatinib of cancers harboring EGFR compound mutations.
脑脊液(CSF)的液体活检和游离DNA测序很少用于鉴定表皮生长因子受体(EGFR)突变,而该突变可为肺腺癌软脑膜转移患者精确、个性化治疗方案的设计提供指导。
一名42岁肺腺癌伴软脑膜转移的女性于2019年3月31日入院。她对吉非替尼、奥希替尼或放化疗均无反应,病情危急,预期生存期<4周。
脑脊液和外周血样本的二代测序鉴定出一种EGFR复合突变(外显子19缺失+K754E)。
2019年4月10日,患者开始口服阿法替尼(40毫克,口服,每日一次),但1周后出现Ⅲ级口腔黏膜反应。阿法替尼剂量减至30毫克,口服,每日一次。
在2019年5月15日的随访检查中,患者报告头痛缓解。增强磁共振成像显示软脑膜异常强化减轻,脑脊液压力和癌胚抗原水平也降低。患者继续接受阿法替尼治疗(30毫克,每日一次),不良反应轻微。
这是首例关于肺腺癌伴软脑膜转移且携带EGFR复合突变(外显子19缺失+K754E)的患者经阿法替尼治疗后临床症状改善的病例报告,从而为携带EGFR复合突变的癌症患者使用阿法替尼治疗提供了临床参考。