Hachlaf Mariem, Lkhoyaali Sihame, Nadir Wydad, Lemsyeh Hajar, El Ghissassi Brahim, Mrabti Hind, Boutayeb Saber, Errihani Hassan
Department of Medical Oncology, National Institute of Oncology, Rabat, Morocco.
J Med Case Rep. 2024 Aug 8;18(1):374. doi: 10.1186/s13256-024-04706-w.
First- and second-generation anti-epithelial growth factor receptor tyrosine kinase inhibitors have shown great efficacy in the treatment of advanced adenocarcinoma with epithelial growth factor receptor mutations, but this efficacy is limited by certain resistance mechanisms, in particular the T790M mutation, which must be screened before second-line treatment with osimertinib is indicated. The search for this mutation is sometimes difficult, especially in cases of intracranial relapse, through this case report we attempt to discuss the possibility of initiating treatment with osimertinib despite an unknown T790M mutation in such situation.
We present the case of a 70-year-old Moroccan male patient diagnosed with non-small cell lung carcinoma initially metastatic to the pleura with an epithelial growth factor receptor mutation who received gefitinib in first line with a complete response, he subsequently presented with cerebral oligo-progression with extra cranial stability. The patient was started on osimertinib with unknown T790M status, as it was impossible to perform a cerebral biopsy, the evolution was characterized by a partial response followed by stereotactic radiotherapy then a complete response for 2 years.
We can discuss osimertinib as an option for patients with stage IV non-small cell lung cancer with brain oligo-progression on prior tyrosine kinase inhibitors and unknown T790M status, further studies are needed in this area.
第一代和第二代抗表皮生长因子受体酪氨酸激酶抑制剂在治疗具有表皮生长因子受体突变的晚期腺癌方面已显示出巨大疗效,但这种疗效受到某些耐药机制的限制,特别是T790M突变,在使用奥希替尼进行二线治疗之前必须进行筛查。寻找这种突变有时很困难,尤其是在颅内复发的情况下,通过本病例报告,我们试图讨论在这种情况下尽管T790M突变未知但仍开始使用奥希替尼治疗的可能性。
我们介绍了一名70岁摩洛哥男性患者的病例,该患者被诊断为非小细胞肺癌,最初转移至胸膜,具有表皮生长因子受体突变,一线接受吉非替尼治疗并获得完全缓解,随后出现脑寡进展伴颅外稳定。患者在T790M状态未知的情况下开始使用奥希替尼,因为无法进行脑活检,病情演变特点为部分缓解,随后进行立体定向放疗,然后完全缓解持续2年。
对于先前接受酪氨酸激酶抑制剂治疗后出现脑寡进展且T790M状态未知的IV期非小细胞肺癌患者,我们可以讨论将奥希替尼作为一种选择,该领域还需要进一步研究。