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阿来替尼在同时存在新型ALK-MTUS2和STRN3-ALK双重融合的晚期肺腺癌中的疗效:一例报告及文献综述

Alectinib efficacy in advanced lung adenocarcinoma with coexistence of a novel ALK-MTUS2 and STRN3-ALK double fusion: A case report and literature review.

作者信息

Qiu Xirui, Wei Yu, Wang Xiaoxiao, Xu Siyan, Zhang Yaru, He Hailang, Zhou Xianmei

机构信息

Department of Respiratory and Critical Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, Jiangsu 210029, P.R. China.

Clinical Research Institute, Affiliated Hospital of Nanjing University of Chinese Medicine, Jiangsu Province Hospital of Chinese Medicine, Nanjing, Jiangsu 210029, P.R. China.

出版信息

Oncol Lett. 2025 Jul 7;30(3):432. doi: 10.3892/ol.2025.15178. eCollection 2025 Sep.

Abstract

In total, >90 unique anaplastic lymphoma kinase (ALK) rearrangement fusion partners have been identified, each with a unique sensitivity to ALK tyrosine kinase inhibitors, rendering targeted therapy challenging. In the present study, the efficacy of alectinib in a patient with advanced lung adenocarcinoma harbouring a novel ALK-microtubule-associated tumour suppressor candidate 2 (MTUS2) fusion and a rare Striatin 3 (STRN3)-ALK fusion was assessed. A 20-year-old non-smoker was hospitalised with a persistent cough. Subsequent positron emission tomography/computed tomography revealed a tumour in the right lower lobe, with mediastinal, hilar, lymph node and bone metastases. Cranial magnetic resonance imaging also revealed a cerebral metastasis. Bronchoscopic biopsy revealed an adenocarcinoma in the right lower lobe nodule, resulting in a clinical stage IVB diagnosis (cT2bN3bM1c). Targeted next-generation sequencing of tissue and blood samples revealed ALK-MTUS2 and STRN3-ALK fusions. The patient was treated with alectinib as the first-line therapy and a durable partial response was achieved after 3 months, with disappearance of the brain metastases. To the best of our knowledge, the present study represents the first discovery of simultaneous ALK-MTUS2 and STRN3-ALK fusions. The clinical outcome offers potential therapeutic options for patients with rare ALK rearrangements and underscores the necessity for further research on the functions of these fusions.

摘要

总共已鉴定出超过90种独特的间变性淋巴瘤激酶(ALK)重排融合伴侣,每种对ALK酪氨酸激酶抑制剂都有独特的敏感性,这使得靶向治疗具有挑战性。在本研究中,评估了阿来替尼对一名患有新型ALK-微管相关肿瘤抑制候选物2(MTUS2)融合和罕见的striatin 3(STRN3)-ALK融合的晚期肺腺癌患者的疗效。一名20岁的不吸烟者因持续咳嗽入院。随后的正电子发射断层扫描/计算机断层扫描显示右下叶有肿瘤,伴有纵隔、肺门、淋巴结和骨转移。头颅磁共振成像还显示有脑转移。支气管镜活检显示右下叶结节为腺癌,临床诊断为IVB期(cT2bN3bM1c)。对组织和血液样本进行靶向二代测序发现了ALK-MTUS2和STRN3-ALK融合。该患者接受阿来替尼作为一线治疗,3个月后取得了持久的部分缓解,脑转移消失。据我们所知,本研究首次发现了同时存在的ALK-MTUS2和STRN3-ALK融合。临床结果为罕见ALK重排患者提供了潜在的治疗选择,并强调了对这些融合功能进行进一步研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a35/12278715/0af733c5f229/ol-30-03-15178-g00.jpg

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