Nasu Shingo, Shiroyama Takayuki, Morita Satomu, Takata So, Takada Hiromune, Masuhiro Kentaro, Tanaka Ayako, Morishita Naoko, Suzuki Hidekazu, Okamoto Norio, Hirashima Tomonori
Department of Thoracic Oncology, Osaka Habikino Medical Center, Japan.
Intern Med. 2018 Dec 15;57(24):3643-3645. doi: 10.2169/internalmedicine.0923-18. Epub 2018 Aug 24.
Epidermal growth factor receptor (EGFR) T790M mutations are the most frequent mechanism of resistance to first- and second-generation tyrosine kinase inhibitors, and osimertinib is an effective treatment for patients with both EGFR-activating mutations and T790M resistance mutations. We describe the case of a 68-year-old woman with lung adenocarcinoma with G719S, S768I, and T790M mutations in which osimertinib treatment was unsuccessful. The patient died of disease progression one month after discontinuing osimertinib treatment. This case suggests that osimertinib may be ineffective for treating patients with uncommon mutations such as G719S when the patient has also acquired a T790M resistance mutation.
表皮生长因子受体(EGFR)T790M突变是对第一代和第二代酪氨酸激酶抑制剂耐药的最常见机制,奥希替尼对具有EGFR激活突变和T790M耐药突变的患者是一种有效的治疗方法。我们描述了一名68岁患有肺腺癌且具有G719S、S768I和T790M突变的女性病例,其中奥希替尼治疗未成功。该患者在停止奥希替尼治疗1个月后死于疾病进展。该病例表明,当患者同时获得T790M耐药突变时,奥希替尼可能对治疗具有如G719S等罕见突变的患者无效。