医学
靶向治疗
肺癌
肿瘤科
癌
肺
化疗
癌症研究
融合基因
内科学
克里唑蒂尼
间变性淋巴瘤激酶
大细胞
放射治疗
病理
癌症
腺癌
基因
生物
生物化学
恶性胸腔积液
作者
Ying Luo,Delong Li,Yang Qi,Youyou Dong,Weijun Chen
标识
DOI:10.1097/cad.0000000000001715
摘要
The prognosis of advanced lung large-cell neuroendocrine carcinoma is poor, and the efficacy of targeted therapy is still being explored. A case of RET fusion mutation combined with ALK rearrangement positive advanced lung complex large cell neuroendocrine carcinoma was reported. The patient developed intrapulmonary and bone metastases 8 months after chemotherapy after lung cancer surgery, RET fusion mutations were detected by genetic testing, and intracranial progression occurred 1 year after pilatinib was applied. The comutation of RET and ALK was detected by genetic testing, and the pulmonary progression occurred 2 months after the application of aletinib, after being treated with pilatinib and aletinib, he progressed again in 9 months. We point out that large cell neuroendocrine carcinoma complex patients with RET gene mutation can benefit from targeted therapy, and when drug resistance is accompanied by ALK comutation, the patient can benefit from the treatment of the aletinib combined with pilatinib targeted therapy and the side effect is slight. At the same time, we further explore the resistance mechanism of targeted therapy in lung cancer.
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