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New guideline sets the ground rules for routine molecular testing in non-small cell lung cancer

机译:新指南为非小细胞肺癌的常规分子检测设定了基本规则

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In the last decade there has been dramatic evolution of our understanding of non-small cell lung cancer (NSCLC). What was once thought of as a single common disease has emerged as a collection of relatively uncommon diseases with different genetic drivers,and the recognition of distinct molecular subtypes of NSCLC has led to the rapid adoption of new targeted drugs for the treatment of patients with epidermal growth factor receptor (EGFR) gene mutations and EML4/ALK gene rearrangements. Although personalized therapy is a worthy goal, the need to identify appropriate patients for molecularly targeted therapy has introduced multiple issues that need to be addressed by both pathologists and treating oncologists. Which NSCLC patients should be tested, how quickly must testing be performed, and when should that testing be performed in the disease process? What techniques are most appropriate, what are the tissue requirements for testing, and how should scarce tissue be prioritized? In an attempt to standardize practices and provide guidance on these issues, the College of American Pathologists (CAP), the International Association for the Study of Lung Cancer (IASLC), and the Association for Molecular Pathology (AMP) have jointly issued a guideline for the selection of lung cancer patients for EGFR and ALK testing that should provide a framework for molecular testing going forward
机译:在过去的十年中,我们对非小细胞肺癌(NSCLC)的理解有了巨大的发展。曾经被认为是一种单一的常见疾病,已经出现了具有不同遗传驱动因素的相对罕见疾病的集合,对NSCLC不同分子亚型的认识已导致迅速采用新的靶向药物来治疗表皮病患者生长因子受体(EGFR)基因突变和EML4 / ALK基因重排。尽管个性化治疗是一个有价值的目标,但确定合适的患者进行分子靶向治疗的需求引入了多个问题,病理学家和肿瘤治疗学家都需要解决。应该检查哪些NSCLC患者,必须多快进行检查以及在疾病过程中应何时进行检查?哪种技术最合适,检测的组织要求是什么,稀缺组织应如何确定优先级?为了规范实践并就这些问题提供指导,美国病理学家学院(CAP),国际肺癌研究协会(IASLC)和分子病理学协会(AMP)共同发布了指南为EGFR和ALK检测选择肺癌患者应为今后的分子检测提供框架

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