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多线系统治疗后晚期非小细胞肺癌中获得性ROS1融合及艾乐替尼反应:一例报告

Acquired ROS1 fusion and iruplinalkib response in advanced NSCLC after multiple lines of systematic therapy: a case report.

作者信息

Liu Jiarui, Jiao Zhichao, Zhou Jun, Yuan Yuan, Li Qiguang, Zhou Wei, Zhang Shuai, Yang Shuping

机构信息

Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.

The Clinical Medical College, Shandong First Medical University (Shandong Academy of Medicine), Jinan, Shandong, China.

出版信息

Front Oncol. 2025 Apr 30;15:1571512. doi: 10.3389/fonc.2025.1571512. eCollection 2025.

Abstract

This is the first report of a patient with lung cancer whose primary focus was the upper lobe of the left lung combined with multiple metastases in both lungs, initially diagnosed as a non-driver gene mutation, who subsequently developed SDC4-ROS1 fusion after multiple lines of systemic therapy. When diagnosis, a needle biopsy of the primary focus revealed no driver gene mutation and low PD-L1 expression (TPS < 1%, CPS 3). From November 2022 to December 2023, the patient received sequential chemotherapy-based systemic therapy including anti-angiogenesis treatment, concurrent chemoradiation and combined immunotherapy as determined by the clinician based on the initial evaluation. In December 2023, a needle biopsy of a metastasis in the left lower lobe of the lung showed a positive SDC4-ROS1 fusion. Subsequent treatment with the oral ALK TKI iruplinalkib was initiated based on the patient's preference, which exhibited a promising response over the next 2 months.

摘要

这是首例原发性病灶位于左肺上叶并伴有双肺多发转移的肺癌患者报告,该患者最初被诊断为无驱动基因突变,在接受多线全身治疗后出现SDC4-ROS1融合。诊断时,对原发性病灶进行穿刺活检未发现驱动基因突变且PD-L1表达低(TPS<1%,CPS 3)。2022年11月至2023年12月,根据临床医生的初步评估,患者接受了以化疗为基础的序贯全身治疗,包括抗血管生成治疗、同步放化疗和联合免疫治疗。2023年12月,对左肺下叶转移灶进行穿刺活检显示SDC4-ROS1融合阳性。随后根据患者意愿开始口服ALK TKI药物艾乐替尼治疗,在接下来的2个月里显示出良好疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cd/12074972/b29fd9fbcecd/fonc-15-1571512-g001.jpg

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