首页> 美国卫生研究院文献>Case Reports in Oncology >Personalized Approach to Tissue and Liquid Biopsy after Failure of First-Line EGFR-TKIs: Is There an Issue When Tissue Is Not the Issue? A Case Series
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Personalized Approach to Tissue and Liquid Biopsy after Failure of First-Line EGFR-TKIs: Is There an Issue When Tissue Is Not the Issue? A Case Series

机译:第一线EGFR-TKIS失败后组织和液体活检的个性化方法:在组织不是问题时有问题吗?案例系列

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摘要

Traditionally, tissue availability from rebiopsy is a prerequisite for adequate sequencing of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in therapy for advanced-stage lung cancer. Tissue biopsy truly is the gold standard for genetic analyses, but in some cases, such as with inadequate localization of the lesion or a patient's inadequate performance status, comorbidities, or unwillingness to undergo an invasive procedure, liquid biopsy-based ctDNA analysis can be a noninvasive alternative approach. However, in some cases the gold standard might not shine that much. It is known that tumor heterogeneity or an inadequate amount of tissue might significantly interfere with the results of testing. In this paper, we present cases of patients with a negative tissue biopsy but a positive liquid biopsy which identified coexisting T790M mutation. These results enabled adequate sequencing and treatment with third-line EGFR-TKIs. Such possibilities stress the need to individualize testing for driver mutations in cases where it is clinically highly indicated.
机译:传统上,来自ReBiopsy的组织可用性是对晚期肺癌治疗中表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIS)的足够序列的先决条件。组织活组织检查真正是遗传分析的金标准,但在某些情况下,例如病变的定位不足或患者不足的性能状态,组合或不愿意进行侵入性程序,基于液检的CTDNA分析可以是a非侵略性的替代方法。但是,在某些情况下,黄金标准可能不会闪耀这么多。众所周知,肿瘤异质性或组织的不足可能会产生显着干扰测试结果。在本文中,我们呈现阴性组织活组织检查患者,但鉴定了共存T790M突变的正液体活组织检查。这些结果使得用第三线EGFR-TKI使能足够的测序和治疗。这种可能性在临床上高度指出的情况下,应力对驾驶员突变进行个性化测试。

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