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阿来替尼治疗携带有 HIP1-ALK(H28:A20)和 CTNNB1 p.S45del 突变的非小细胞肺癌患者获得成功。

Successful treatment of a non-small-cell lung cancer patient harboring HIP1-ALK (H28:A20) and CTNNB1 p.S45del with alectinib.

机构信息

Thoracic Oncology Unit, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Molecular Diagnostics and Pharmacogenetics Unit, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

出版信息

Thorac Cancer. 2024 Nov;15(31):2283-2287. doi: 10.1111/1759-7714.15397. Epub 2024 Sep 24.

Abstract

This is the first case report of a non-small-cell lung cancer (NSCLC) patient harboring HIP1-ALK (H28:A20) and CTNNB1 p.S45del treated with first-line alectinib. Approximately 5% of NSCLC patients are reported to have anaplastic lymphoma kinase (ALK) rearrangements, and among these EML4-ALK is the most frequent fusion variant. However, in recent years the use of next-generation sequencing (NGS) in clinical laboratories has become increasingly widespread, identifying a lot of new ALK fusion partners as well as a large quantity of co-occurring genomic alterations. Unfortunately, the growing number of genomic alterations detected by NGS does not always correspond to adequate knowledge of their clinical significance, often resulting in an empiric treatment of patients harboring uncommon mutations.

摘要

这是首例报道的接受一线阿来替尼治疗的携带有 HIP1-ALK(H28:A20)和 CTNNB1 p.S45del 的非小细胞肺癌(NSCLC)患者。约 5%的 NSCLC 患者报告存在间变性淋巴瘤激酶(ALK)重排,其中 EML4-ALK 是最常见的融合变异体。然而,近年来,下一代测序(NGS)在临床实验室中的应用越来越广泛,不仅鉴定了许多新的 ALK 融合伙伴,还发现了大量同时存在的基因组改变。不幸的是,NGS 检测到的越来越多的基因组改变并不总是与其临床意义相匹配,这通常导致对携带罕见突变的患者进行经验性治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11543270/b9345ac6667b/TCA-15-2283-g002.jpg

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