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

机译:带有汽车 - ALK融合的转移性低级肉瘤患有多种ALK酪氨酸激酶抑制剂:案例报告综合基因组分析

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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.
机译:本文报告了一个先进的转移性低级肉瘤案例。患者于2015年9月在他的颈部诊断出患有不可操作的大(14倍12厘米)病变,并在下面的4个月内完成了两种无效化学疗法。有趣的是,虽然有几位病理学家不能达到组织病理学诊断,但使用下一代测序(NGS)获得精确的分子病理诊断,最终呈现出优异的治疗效果。检测患者以通过NGS进行汽车 - ALK融合,然后口服CRIZOTINIB成功处理。他在肿瘤收缩后接受了初级和转移性病变的手术切除。组合治疗带来了40个月的持久反应。虽然肿瘤于2019年7月重复,但患者对迄今为止迄今为止对二线烷基酪氨酸激酶抑制剂抑制剂良好响应。我们对患者的主要,转移性和复发性肿瘤进行了全基因组测序,并进行了综合基因组分析。此外,我们的分析结果表明,在这种情况的肿瘤内发生期间可能发生了整个基因组重复事件。关键指出我们最佳知识,这是第一份关于汽车-ALK融合阳性转移性低级肉瘤的第一和第二型alk酪氨酸激酶抑制剂的非常成功的治疗报告。分子病理结果可以指导肉瘤的精度治疗,即使不能获得精确的组织病理学。使用全基因组测序分析来自该患者的多个样品。结果提供了详细的基因组特征,并显示出这种低级肉瘤病例的肿瘤演变。在这种低级肉瘤案例的肿瘤内发生过程中可能发生了整个基因组复制事件。

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