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转移性低度恶性肉瘤伴 CARS-ALK 融合对多种 ALK 酪氨酸激酶抑制剂有显著反应:一例综合基因组分析的病例报告。

Metastatic Low-Grade Sarcoma with CARS-ALK Fusion Dramatically Responded to Multiple ALK Tyrosine Kinase Inhibitors: A Case Report with Comprehensive Genomic Analysis.

机构信息

Department of Medical Oncology, Changzheng Hospital, Shanghai, People's Republic of China.

HaploX Biotechnology, Shenzhen, People's Republic of China.

出版信息

Oncologist. 2021 Apr;26(4):e524-e529. doi: 10.1002/onco.13543. Epub 2020 Oct 16.

Abstract

This article reports a case of advanced metastatic low-grade sarcoma. The patient was diagnosed with an inoperable large (14 × 12 cm) lesion on his neck in September 2015 and underwent two ineffective chemotherapies in the following 4 months. Interestingly, although several pathologists could not agree on the histopathological diagnosis, the precise molecular pathological diagnosis was obtained using next-generation sequencing (NGS) and finally brought excellent therapeutic effects. The patient was detected to have CARS-ALK fusion by NGS and then was successfully treated with crizotinib orally. He received surgical resection of primary and metastatic lesions after tumor shrinkage. The combined treatment brought a durable response for 40 months. Although the tumor recurred in July 2019, the patient has been responding well to the second-line ALK tyrosine kinase inhibitor alectinib to date. We performed whole genome sequencing on the patient's primary, metastatic, and recurrent tumors and did comprehensive genomic analysis. Furthermore, our analysis results revealed that a whole genome duplication event might have happened during tumorigenesis of this case. KEY POINTS: To our best knowledge, this is the first report of a very successful treatment with first- and second-line ALK tyrosine kinase inhibitors for CARS-ALK fusion-positive metastatic low-grade sarcoma. Molecular pathological result can guide precision treatment for sarcoma, even when the exact histopathology cannot be obtained. Multiple samples from this patient were analyzed using whole genome sequencing. Results provided detailed genomic characteristics and showed tumor evolution of this low-grade sarcoma case. A whole genome duplication event might have happened during tumorigenesis of this low-grade sarcoma case.

摘要

这篇文章报道了一例晚期转移性低度恶性肉瘤病例。患者于 2015 年 9 月被诊断为颈部不可手术的大型(14×12cm)病变,并在接下来的 4 个月中接受了两次无效的化疗。有趣的是,尽管有几位病理学家无法对组织病理学诊断达成一致意见,但通过下一代测序(NGS)获得了精确的分子病理诊断,最终带来了极佳的治疗效果。该患者通过 NGS 检测到 CARS-ALK 融合,然后成功接受了克唑替尼口服治疗。在肿瘤缩小后,他接受了原发和转移病灶的手术切除。联合治疗带来了长达 40 个月的持久缓解。尽管该肿瘤于 2019 年 7 月复发,但迄今为止,患者对二线 ALK 酪氨酸激酶抑制剂阿来替尼的反应良好。我们对患者的原发、转移和复发性肿瘤进行了全基因组测序,并进行了全面的基因组分析。此外,我们的分析结果表明,该病例在肿瘤发生过程中可能发生了全基因组复制事件。

关键点

据我们所知,这是首例采用一线和二线 ALK 酪氨酸激酶抑制剂成功治疗 CARS-ALK 融合阳性转移性低度恶性肉瘤的病例报告。即使无法获得确切的组织病理学结果,分子病理学结果也可以指导肉瘤的精准治疗。对该患者的多个样本进行了全基因组测序分析。结果提供了详细的基因组特征,并显示了该低度恶性肉瘤病例的肿瘤演变。该低度恶性肉瘤病例的肿瘤发生过程中可能发生了全基因组复制事件。

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1
Pan-cancer whole-genome analyses of metastatic solid tumours.泛癌种实体瘤全基因组分析。
Nature. 2019 Nov;575(7781):210-216. doi: 10.1038/s41586-019-1689-y. Epub 2019 Oct 23.
2
fastp: an ultra-fast all-in-one FASTQ preprocessor.fastp:一个超快速的一体化 FASTQ 预处理程序。
Bioinformatics. 2018 Sep 1;34(17):i884-i890. doi: 10.1093/bioinformatics/bty560.
3
Strelka2: fast and accurate calling of germline and somatic variants.Strelka2:快速准确地调用种系和体细胞变异。
Nat Methods. 2018 Aug;15(8):591-594. doi: 10.1038/s41592-018-0051-x. Epub 2018 Jul 16.

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