Department of Medical Oncology, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Anticancer Drugs. 2022 Jan 1;33(1):e730-e733. doi: 10.1097/CAD.0000000000001159.
EGFR and BRAF V600E mutations are both early driven and usually mutually exclusive. We report the case of a 59-year-old woman diagnosed with advanced lung adenocarcinoma harboring coexisting EGFR exon 18 G719A and BRAF V600E mutations. She experienced a long-term response to oral afatinib, with a progression-free survival rate of 33 months and an overall survival rate of 11 years. Lung adenocarcinoma with synchronous EGFR G719A and BRAF V600E mutations is rare and has not been previously reported. This case highlights the importance of an adequate response to afatinib and provides an optimal therapeutic option for such patients.
EGFR 和 BRAF V600E 突变都是早期驱动因素,通常相互排斥。我们报告了一例 59 岁女性,被诊断为晚期肺腺癌,同时存在 EGFR 外显子 18 G719A 和 BRAF V600E 突变。她对口服阿法替尼有长期反应,无进展生存期为 33 个月,总生存期为 11 年。同时存在 EGFR G719A 和 BRAF V600E 突变的肺腺癌很少见,以前没有报道过。该病例强调了阿法替尼充分应答的重要性,并为此类患者提供了最佳治疗选择。