de Jager Vincent D, Stigt Jos A, Niemantsverdriet Maarten, Ter Elst Arja, van der Wekken Anthonie J
Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Department of Respiratory Medicine, Isala Hospital, Zwolle, The Netherlands.
NPJ Precis Oncol. 2024 May 22;8(1):113. doi: 10.1038/s41698-024-00607-9.
Precision cancer medicine has changed the treatment paradigm of patients with non-small cell lung cancer (NSCLC) with specific molecular aberrations. A major challenge is management of the resistance that tumor cells eventually develop against targeted therapies, either through primary or acquired resistance mechanisms. We report a 61 year-old male patient with metastatic NSCLC harboring an EGFR exon 19 deletion, a PIK3CA mutation, and CDK4 amplification. After an initial partial response to osimertinib as mono-therapy (third-generation EGFR tyrosine kinase inhibitor), the patient had progression of disease after 4 months of treatment and was referred for combined osimertinib and palbociclib (CDK4/6 inhibitor) treatment. Though complicated by transient pneumonitis, the patient has an ongoing partial response for > 10 months and has experienced clinical improvement on this treatment regimen. As amplification of CDK4 occurs in ~ 10% of treatment-naïve patients with EGFR-mutated NSCLC, the successful treatment of our patient with osimertinib and palbociclib may be highly relevant for future patients with NSCLC.
精准癌症医学已经改变了具有特定分子异常的非小细胞肺癌(NSCLC)患者的治疗模式。一个主要挑战是肿瘤细胞最终通过原发性或获得性耐药机制对靶向治疗产生的耐药性管理。我们报告了一名61岁的男性转移性NSCLC患者,其携带EGFR外显子19缺失、PIK3CA突变和CDK4扩增。在作为单一疗法使用奥希替尼(第三代EGFR酪氨酸激酶抑制剂)最初出现部分缓解后,患者在治疗4个月后疾病进展,并被转诊接受奥希替尼和哌柏西利(CDK4/6抑制剂)联合治疗。尽管出现了短暂性肺炎的并发症,但该患者持续部分缓解超过10个月,并且在此治疗方案下病情得到了临床改善。由于在约10%未经治疗的EGFR突变NSCLC患者中会出现CDK4扩增,我们的患者使用奥希替尼和哌柏西利成功治疗可能与未来的NSCLC患者高度相关。