Cekay Michael, Arndt Philipp F, Dumitrascu Rio, Savai Rajkumar, Braeuninger Andreas, Gattenloehner Stefan, Steiner Dagmar, Roller Fritz, Tello Khodr, Hattar Katja, Seeger Werner, Sibelius Ulf, Grimminger Friedrich, Eul Bastian
Department of Internal Medicine, Justus-Liebig-University Giessen, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Giessen, Germany.
Max Planck Institute for Heart and Lung Research, Member of the DZL, Member of CPI, Giessen, Germany.
Front Oncol. 2023 Aug 16;13:1182391. doi: 10.3389/fonc.2023.1182391. eCollection 2023.
Up to 20% of all non-small cell lung cancer patients harbor tumor specific driver mutations that are effectively treated with tyrosine kinase inhibitors. However, for the rare EGFR deletion-insertion mutation of exon 18, there is very little evidence regarding the effectiveness of tyrosine kinase inhibitors. A particular challenge for clinicians in applying tyrosine kinase inhibitors is not only diagnosing a mutation but also interpreting rare mutations with unclear therapeutic significance. Thus, we present the case of a 65-year-old Caucasian male lung adenocarcinoma patient with an EGFR Exon 18 p.Glu709_Thr710delinsAsp mutation of uncertain therapeutic relevance. This patient initially received two cycles of standard platinum-based chemotherapy without any therapeutic response. After administration of Osimertinib as second line therapy, the patient showed a lasting partial remission for 12 months. Therapy related toxicities were limited to mild thrombocytopenia, which ceased after dose reduction of Osimertinib. To our knowledge, this is the first report of effective treatment of this particular mutation with Osimertinib. Hence, we would like to discuss Osimertinib as a viable treatment option in EGFR Exon 18 p.Glu709_Thr710delinsAsp mutated lung adenocarcinoma.
高达20%的非小细胞肺癌患者携带肿瘤特异性驱动突变,可通过酪氨酸激酶抑制剂进行有效治疗。然而,对于罕见的18号外显子EGFR缺失插入突变,关于酪氨酸激酶抑制剂有效性的证据非常少。临床医生在应用酪氨酸激酶抑制剂时面临的一个特殊挑战不仅是诊断突变,还包括解读治疗意义不明确的罕见突变。因此,我们报告一例65岁白种人男性肺腺癌患者,其携带EGFR 18号外显子p.Glu709_Thr710delinsAsp突变,治疗相关性不确定。该患者最初接受了两个周期的标准铂类化疗,无任何治疗反应。在给予奥希替尼作为二线治疗后,患者出现了持续12个月的部分缓解。治疗相关毒性仅限于轻度血小板减少,在奥希替尼剂量减少后停止。据我们所知,这是首例用奥希替尼有效治疗该特定突变的报告。因此,我们想讨论奥希替尼作为EGFR 18号外显子p.Glu709_Thr710delinsAsp突变的肺腺癌的一种可行治疗选择。