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[塞瑞替尼作为伴有COX7A2L-ALK融合的晚期肺腺癌一线治疗:一例报告及文献综述]

[Ceritinib as First-line Treatment for Advanced Lung Adenocarcinoma 
with COX7A2L-ALK Fusion: A Case Report and Literature Review].

作者信息

Yuan Jiao, Pan Ruili, Zhong Wei, Wang Mengzhao

机构信息

Department of Respiratory Disease, Chengdu Seventh People's Hospital, Chengdu 610213, China.

Department of Pulmonary and Critic Care Medicine, Peking Union Medical College Hospital, Peking Union Medical College and Chinses Academy of Medical Science, Beijing 100730, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2023 Apr 20;26(4):319-324. doi: 10.3779/j.issn.1009-3419.2023.102.15.

Abstract

Lung cancer is the most common in incidence and mortality worldwide. With the development of next generation sequencing (NGS) detection technology, more and more patients with rare anaplastic lymphoma kinase (ALK) fusion mutations were detected. A case of advanced lung adenocarcinoma with rare COX7A2L-ALK (C2:A20) fusion detected by NGS was reported in Peking Union Medical College Hospital, and all cases with rare ALK fusion mutations were searched from medical datebase from January 1, 2014 to March 31, 2021, to investigate the treatment of rare ALK fusion mutations with ALK inhibitors. The best response of the patient was assessed as partial response (PR) with Ceritinib treatment. By literature review, 22 cases of rare ALK fusion were reported in 19 articles. Combined with this case, 23 cases were analyzed. The objective response rate (ORR) was 82.6% (19/23) and disease control rate (DCR) was 95.7% (22/23) for rare ALK fusions patients treated with ALK inhibitors. Lung adenocarcinoma patients with rare ALK fusion could benefit from ALK inhibitors.
.

摘要

肺癌是全球发病率和死亡率最高的癌症。随着下一代测序(NGS)检测技术的发展,越来越多罕见的间变性淋巴瘤激酶(ALK)融合突变患者被检测出来。北京协和医院报告了1例通过NGS检测到罕见的COX7A2L-ALK(C2:A20)融合的晚期肺腺癌病例,并从2014年1月1日至2021年3月31日的医学数据库中搜索了所有罕见ALK融合突变病例,以研究使用ALK抑制剂治疗罕见ALK融合突变的情况。该患者使用色瑞替尼治疗的最佳反应评估为部分缓解(PR)。通过文献回顾,19篇文章报道了22例罕见ALK融合病例。结合本病例,共分析了23例。接受ALK抑制剂治疗的罕见ALK融合患者的客观缓解率(ORR)为82.6%(19/23),疾病控制率(DCR)为95.7%(22/23)。具有罕见ALK融合的肺腺癌患者可从ALK抑制剂中获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb44/10186266/654b52dcc400/img_1.jpg

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本文引用的文献

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Lung adenocarcinoma with a novel SRBD1-ALK Fusion responding to crizotinib.
Lung Cancer. 2020 Aug;146:370-372. doi: 10.1016/j.lungcan.2020.04.031. Epub 2020 May 4.
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A novel EML4-ALK BIRC6-ALK double fusion variant in lung adenocarcinoma confers sensitivity to alectinib.
Lung Cancer. 2020 Jul;145:211-212. doi: 10.1016/j.lungcan.2020.04.030. Epub 2020 May 4.
6
A novel SOS1-ALK fusion variant in a patient with metastatic lung adenocarcinoma and a remarkable response to crizotinib.
Lung Cancer. 2020 Apr;142:59-62. doi: 10.1016/j.lungcan.2020.02.012. Epub 2020 Feb 21.
7
The clinical responses of TNIP2-ALK fusion variants to crizotinib in ALK-rearranged lung adenocarcinoma.
Lung Cancer. 2019 Nov;137:19-22. doi: 10.1016/j.lungcan.2019.08.032. Epub 2019 Aug 31.

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