Inagaki Yuji, Tamiya Akihiro, Matsuda Yoshinobu, Azuma Kouji, Adachi Yuichi, Enomoto Takatoshi, Kouno Shunichi, Taniguchi Yoshihiko, Saijo Nobuhiko, Okishio Kyoichi, Atagi Shinji
Department of Internal Medicine.
Department of Psychosomatic Internal Medicine.
Medicine (Baltimore). 2020 Oct 16;99(42):e22628. doi: 10.1097/MD.0000000000022628.
The clinical efficacy of osimertinib for patients with lung adenocarcinoma harboring epidermal growth factor receptor (EGFR) exon 20 insertion mutations is unclear. Few case reports exist on the successful treatment of such tumors with osimertinib. We report a case wherein osimertinib administration had no effect in a patient with EGFR exon 20 insertion-positive lung adenocarcinoma.
A 48-year-old never-smoking woman was referred to our hospital for chronic cough. Computed tomography (CT) and positron emission tomography-CT revealed a nodule in the right middle lobe, consolidation in the right upper lobe, multiple lymph node metastases, liver metastasis, and multiple bone metastases.
On the basis of further examination using transbronchial lung biopsy, the patient was diagnosed with cT1N3M1 stage IVB lung adenocarcinoma. An EGFR exon 20 insertion, without any additional mutations, was identified.
Daily oral administration of 80 mg osimertinib was initiated to treat the EGFR exon 20 insertion-positive lung adenocarcinoma.
Although the disease appeared to be stable 2.5 months after the administration of osimertinib, the tumor started to grow 3 months after administration, and carcinoembryonic antigen levels became higher than those before treatment. Thus, osimertinib was discontinued, and treatment with carboplatin as well as pemetrexed and bevacizumab was started, which the patient responded to.
EGFR exon 20 insertion mutations must be classified in more detail to assess the efficacy of EGFR tyrosine kinase inhibitors. Osimertinib doses that provide favorable therapeutic windows should be considered. Further clinical research is required to clarify the efficacy of osimertinib and other drugs for exon 20 insertion mutations.
奥希替尼对携带表皮生长因子受体(EGFR)外显子20插入突变的肺腺癌患者的临床疗效尚不清楚。关于使用奥希替尼成功治疗此类肿瘤的病例报告很少。我们报告一例奥希替尼治疗EGFR外显子20插入阳性肺腺癌患者无效的病例。
一名48岁从不吸烟的女性因慢性咳嗽转诊至我院。计算机断层扫描(CT)和正电子发射断层扫描-CT显示右中叶有一个结节,右上叶实变,多发淋巴结转移、肝转移和多发骨转移。
通过经支气管肺活检进一步检查,患者被诊断为cT1N3M1 ⅣB期肺腺癌。检测到EGFR外显子20插入,无其他突变。
开始每日口服80毫克奥希替尼治疗EGFR外显子20插入阳性肺腺癌。
虽然在服用奥希替尼2.5个月后疾病似乎稳定,但服药3个月后肿瘤开始生长,癌胚抗原水平高于治疗前。因此,停用奥希替尼,开始使用卡铂以及培美曲塞和贝伐单抗治疗,患者对此有反应。
必须更详细地对EGFR外显子20插入突变进行分类,以评估EGFR酪氨酸激酶抑制剂的疗效。应考虑能提供良好治疗窗的奥希替尼剂量。需要进一步的临床研究来阐明奥希替尼和其他药物对外显子20插入突变的疗效。