Zhang Yu, Zhang Hui, Zhong Wei, Chen Minjiang, Wang Mengzhao
Department of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Zhongguo Fei Ai Za Zhi. 2025 May 20;28(5):400-404. doi: 10.3779/j.issn.1009-3419.2025.102.14.
Immune checkpoint inhibitors (ICIs) have become the cornerstone of treatment for driver gene-negative advanced non-small cell lung cancer (NSCLC). However, resistance is inevitable, and the underlying mechanisms remain incompletely understood. Histological transformation is a rare but emerging cause of acquired resistance to immunotherapy, with only sporadic case reports documented to date. Here, we report the first case of lung adenocarcinoma that underwent histological transformation to atypical carcinoid following first-line therapy with ICIs combined with chemotherapy, highlighting the critical role of histological lineage switching in mediating NSCLC resistance to ICIs. Notably, the patient harbored a rearranged during transfection (RET) fusion mutation. Subsequent targeted therapy with Selpercatinib after histological transformation demonstrated favorable efficacy, suggesting a potential therapeutic strategy for atypical carcinoid patients with co-occurring rare driver mutations. This case provides a potential therapeutic option for atypical carcinoid patients with rare mutations. .
免疫检查点抑制剂(ICIs)已成为驱动基因阴性的晚期非小细胞肺癌(NSCLC)治疗的基石。然而,耐药是不可避免的,其潜在机制仍未完全明确。组织学转化是免疫治疗获得性耐药的一种罕见但新出现的原因,迄今为止仅有零星病例报告。在此,我们报告首例肺腺癌患者,其在接受ICIs联合化疗一线治疗后发生组织学转化为非典型类癌,突出了组织学谱系转换在介导NSCLC对ICIs耐药中的关键作用。值得注意的是,该患者存在转染重排(RET)融合突变。组织学转化后使用塞尔帕替尼进行后续靶向治疗显示出良好疗效,提示对于同时存在罕见驱动突变的非典型类癌患者有潜在治疗策略。该病例为具有罕见突变的非典型类癌患者提供了一种潜在治疗选择。