[肺癌分子诊断及其临床意义]。

Q4 Medicine
Magyar onkologia Pub Date : 2020-09-23 Epub Date: 2020-08-10
József Tímár, Gábor Méhes, László Vass
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引用次数: 0

摘要

肺癌的分子分类在过去几十年中发展到甚至包括罕见的遗传改变的水平。不幸的是,腺癌几乎完全受益于这种发展。此外,肿瘤不可知的新治疗指征影响肺癌的分子诊断,包括微卫星状态、肿瘤突变负荷或NTRK融合基因测定。另一方面,肺癌的切除率仍然很低,可诊断的肿瘤组织有限,为液体活检技术的常规应用开辟了道路。靶向治疗的常规使用引发了各种遗传耐药机制的发展,对其监测逐渐成为疾病监测的标准。除了“靶向”诊断之外,多基因面板检测或全外显子组测序更为频繁,从而导致肺癌的遗传图谱更为复杂。这就需要在分子病理学报告中将基因改变分类为标准、研究性或假设的靶向治疗的预测水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Molecular diagnostics of lung cancer and its clinical relevance].

Molecular classification of lung cancer developed in the past decades to the level where even the rare genetic alterations are included. Unfortunately, adenocarcinoma benefited from this development almost exclusively. Furthermore, the tumor-agnostic novel therapy indications influence the molecular diagnostics of lung cancer including microsatellite status, tumor mutation burden or NTRK fusion gene determinations. On the other hand, the still low resection rate of lung cancer and limited availability of tumor tissue for diagnosis opened the way of routine use of liquid biopsy technologies. The routine use of target therapies triggered the development of various genetic resistance mechanisms, the monitoring of which gradually became a standard of monitoring of the disease. Beside the "targeted" diagnostics, multigene panel testing or whole exome sequencing are more frequent, resulting in a more complex genetic picture of lung cancer. This requires the categorization of genetic alterations into predictive levels for standard, investigational or hypothetic target therapies in the molecular pathology reports.

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来源期刊
Magyar onkologia
Magyar onkologia Medicine-Medicine (all)
CiteScore
0.60
自引率
0.00%
发文量
30
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