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一例携带 CD74-NRG1 融合蛋白和 HER2 突变的多原发肺腺癌患者从联合靶向治疗中获益。

A case of multiple primary lung adenocarcinoma with a CD74-NRG1 fusion protein and HER2 mutation benefit from combined target therapy.

机构信息

Department of Oncology, Beijing Chaoyang San Huan Cancer Hospital, Beijing, China.

State Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Thorac Cancer. 2022 Nov;13(21):3063-3067. doi: 10.1111/1759-7714.14636. Epub 2022 Sep 12.

DOI:10.1111/1759-7714.14636
PMID:36096509
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9626339/
Abstract

Neuregulin 1 (NRG1) gene fusion is a rare oncogenic driver gene in multiple tumor types, leading to the activation of the epidermal growth factor receptor (ErbB)-mediated pathway. Therefore, afatinib, a pan-ErbB family inhibitor, may be a therapeutic candidate for NRG1 fusion-driven tumors. In this case, we report a multiple primary lung adenocarcinoma patient harboring the CD74-NRG1 fusion, epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 2 (ERBB2) mutation simultaneously. The patient received afatinib and pyrotinib combination therapy and showed a significant treatment response with a progression-free survival of 5 months. Our case further supports the use of targeted therapy for NRG1 fusion-positive non-small-cell lung cancer.

摘要

神经调节蛋白 1(NRG1)基因融合是多种肿瘤类型中罕见的致癌驱动基因,导致表皮生长因子受体(ErbB)介导的途径激活。因此,泛 ErbB 家族抑制剂阿法替尼可能是 NRG1 融合驱动肿瘤的治疗候选药物。在本例中,我们报告了一例同时携带 CD74-NRG1 融合、表皮生长因子受体(EGFR)和人表皮生长因子受体 2(ERBB2)突变的多原发肺腺癌患者。该患者接受了阿法替尼和吡咯替尼联合治疗,无进展生存期为 5 个月,显示出显著的治疗反应。我们的病例进一步支持针对 NRG1 融合阳性非小细胞肺癌的靶向治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61c0/9626339/d5e850f81217/TCA-13-3063-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61c0/9626339/d5e850f81217/TCA-13-3063-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61c0/9626339/d5e850f81217/TCA-13-3063-g002.jpg

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