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两例肺腺癌患者分别存在新型 ALK-SSH2、EML4-ALK 和 ARID2-ALK、EML4-ALK 双重融合变异,对克唑替尼敏感。

Concomitant novel ALK-SSH2, EML4-ALK and ARID2-ALK, EML4-ALK double-fusion variants and confer sensitivity to crizotinib in two lung adenocarcinoma patients, respectively.

机构信息

Department of Oncology, Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing, China.

Department of Pathology, Beijing Key Laboratory for Drug Resistant Tuberculosis Research, Beijing Chest Hospital, Capital Medical University, Thoracic Tumor Research Institute, Beijing Tuberculosis, Beijing, China.

出版信息

Diagn Pathol. 2022 Feb 10;17(1):27. doi: 10.1186/s13000-022-01212-9.

Abstract

INTRODUCTION

Anaplastic lymphoma kinase (ALK) gene rearrangements, have been identified in approximately 2-7% of patients with lung adenocarcinoma (LUAD). However, co-occurrence of double ALK fusions in one patient was rare. Herein, we reported two Chinese female LUAD patients with confirmed double ALK fusion variants by next generation sequencing.

CASE PRESENTATION

Case 1, a 38-year-old female was diagnosed as peripheral LUAD in left upper lobe with synchronous multiple intrapulmonary metastases (pT2N0M1b, stage IVa). And case 2, a 58-year-old female had left lower lobe primary LUAD and synchronous multiple lung metastases (pT4N2M1b, stage IVa). In both patients, tumor cells displayed strong expression of ALK protein. Genetic profiling by next generation sequencing showed both patients concurrently harbored two types of ALK rearrangements. Case 1 had an unreported ALK-SSH2/EML4-ALK double fusions, and case 2 had an another novel ARID2-ALK/EML4-ALK double fusions. Both of these patients responded to ALK inhibitor crizotinib.

CONCLUSIONS

Our study reported two novel ALK fusion partners never reported, which expands the knowledge of ALK fusion spectrum and provides insight into therapeutic options for patients with double ALK fusions.

摘要

简介

间变性淋巴瘤激酶(ALK)基因重排约见于 2%-7%的肺腺癌(LUAD)患者。然而,同一患者中同时存在两种 ALK 融合的情况较为罕见。本研究通过下一代测序,报道了两例经证实存在双重 ALK 融合变异的中国女性 LUAD 患者。

病例报告

病例 1,38 岁女性,左肺上叶周围型 LUAD 合并同步多发肺内转移(pT2N0M1b,IVa 期)。病例 2,58 岁女性,左肺下叶原发性 LUAD 合并同步多发肺转移(pT4N2M1b,IVa 期)。两名患者的肿瘤细胞均显示 ALK 蛋白强表达。通过下一代测序进行基因谱分析显示,两名患者均同时存在两种类型的 ALK 重排。病例 1 存在一种未报道的 ALK-SSH2/EML4-ALK 双重融合,病例 2 存在另一种新型 ARID2-ALK/EML4-ALK 双重融合。这两名患者均对 ALK 抑制剂克唑替尼有反应。

结论

本研究报道了两种从未报道过的新的 ALK 融合伙伴,这扩展了 ALK 融合谱的知识,并为双重 ALK 融合患者的治疗选择提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d6/8832643/a817b011e011/13000_2022_1212_Fig1_HTML.jpg

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