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对艾乐替尼治疗有良好应答的 STRN-ALK  融合突变肺腺癌: 病例报告和文献综述

 

Authors Su C, Jiang Y, Jiang W, Wang H, Liu S, Shao Y, Zhao W, Ning R, Yu Q

Received 19 September 2020

Accepted for publication 6 November 2020

Published 4 December 2020 Volume 2020:13 Pages 12515—12519

DOI https://doi.org/10.2147/OTT.S282933

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Prof. Dr. Takuya Aoki


Abstract: Non-small cell lung cancer (NSCLC) patients with anaplastic lymphoma kinase (ALK ) rearrangement benefit from treatment with ALK inhibitors. Therefore, the identification of druggable ALK  fusions is necessary for NSCLC treatment. More than 90 fusion partners of ALK  have been reported in NSCLC patients, but the striatin gene (STRN )-ALK  fusion has rarely been reported. Moreover, the response of STRN -ALK  fusion patients treated with ALK inhibitors remains to be explored. A 64-year-old Chinese male with no history of smoking or alcohol consumption was diagnosed as stage IVB lung adenocarcinoma (LADC) (cT4N3M1c) in October 2018. Next-generation sequencing (NGS) targeting 425 cancer-related genes was performed on the plasma and supernatant of pleural effusion samples and revealed an STRN -ALK  fusion. The patient received alectinib (600 mg, twice daily) as the first-line treatment with an excellent response exceeding 19 months. This is the first report of a NSCLC patient harboring an STRN -ALK  fusion and exhibiting an excellent response to alectinib treatment. This case provides valuable information for therapeutic decision-making of patients with STRN -ALK  fusions. Furthermore, this case also highlighted the advantage of performing targeted NGS on circulating tumor DNA for the identification and analysis of rare, druggable genomic alterations.
Keywords: lung adenocarcinoma, STRN -ALK  fusion, ctDNA, alectinib, targeted NGS