Journal article

Case Report: Durable therapy response to Osimertinib in rare EGFR Exon 18 mutated NSCLC


Authors listCekay, 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

Publication year2023

JournalFrontiers in Oncology

Volume number13

ISSN2234-943X

Open access statusGold

DOI Linkhttps://doi.org/10.3389/fonc.2023.1182391

PublisherFrontiers Media


Abstract
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.



Citation Styles

Harvard Citation styleCekay, M., Arndt, P., Dumitrascu, R., Savai, R., Braeuninger, A., Gattenloehner, S., et al. (2023) Case Report: Durable therapy response to Osimertinib in rare EGFR Exon 18 mutated NSCLC, Frontiers in Oncology, 13, Article 1182391. https://doi.org/10.3389/fonc.2023.1182391

APA Citation styleCekay, M., Arndt, P., Dumitrascu, R., Savai, R., Braeuninger, A., Gattenloehner, S., Steiner, D., Roller, F., Tello, K., Hattar, K., Seeger, W., Sibelius, U., Grimminger, F., & Eul, B. (2023). Case Report: Durable therapy response to Osimertinib in rare EGFR Exon 18 mutated NSCLC. Frontiers in Oncology. 13, Article 1182391. https://doi.org/10.3389/fonc.2023.1182391


Last updated on 2025-10-06 at 11:57