Bao Hejing, Zhang Jiani, Wang Yuhuan, Chen Zhiting, Luo Xi, Li Ting, Su Haoran, Bao Hehong, Cao Xiaolong, Lin Liping
Department of Oncology, The Affiliated Panyu Center Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Cancer Institute of Panyu, Guangzhou, Guangdong, China.
Front Pharmacol. 2024 Nov 28;15:1448291. doi: 10.3389/fphar.2024.1448291. eCollection 2024.
We report a case of an advanced non-small cell lung cancer (NSCLC) patient with brain metastasis, RET fusion, and high expression of programmed death ligand 1 (PD-L1) at initial treatment. After receiving radiotherapy for the brain metastasis, the patient started with anlotinib and added immunotherapy with sintilimab. The patient had a good response to anlotinib and sintilimab treatment, tolerated the adverse reactions, and had a progression-free survival (PFS) of over 17 months. To the best of our knowledge, this is the first clinical case report in the literature describing the benefit of anlotinib and sintilimab treatment for non-small cell lung cancer with RET fusion and high PD-L1 expression. This study explores the biomarker selection for targeted therapy and combined immunotherapy in NSCLC patients.
我们报告了一例晚期非小细胞肺癌(NSCLC)患者,该患者在初始治疗时伴有脑转移、RET融合以及程序性死亡配体1(PD-L1)高表达。在接受脑转移放疗后,患者开始使用安罗替尼,并加用信迪利单抗进行免疫治疗。患者对安罗替尼和信迪利单抗治疗反应良好,耐受不良反应,无进展生存期(PFS)超过17个月。据我们所知,这是文献中首例描述安罗替尼和信迪利单抗治疗RET融合且PD-L1高表达的非小细胞肺癌疗效的临床病例报告。本研究探索了非小细胞肺癌患者靶向治疗和联合免疫治疗的生物标志物选择。