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非小细胞肺癌的诊断和预测免疫组织化学

Diagnostic and Predictive Immunohistochemistry for Non-Small Cell Lung Carcinomas.

机构信息

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

出版信息

Adv Anat Pathol. 2018 Nov;25(6):374-386. doi: 10.1097/PAP.0000000000000206.

DOI:10.1097/PAP.0000000000000206
PMID:30188361
Abstract

Non-small cell lung carcinoma (NSCLC) accounts for significant morbidity and mortality worldwide, with most patients diagnosed at advanced stages and managed increasingly with targeted therapies and immunotherapy. In this review, we discuss diagnostic and predictive immunohistochemical markers in NSCLC, one of the most common tumors encountered in surgical pathology. We highlight 2 emerging diagnostic markers: nuclear protein in testis (NUT) for NUT carcinoma; SMARCA4 for SMARCA4-deficient thoracic tumors. Given their highly aggressive behavior, proper recognition facilitates optimal management. For patients with advanced NSCLCs, we discuss the utility and limitations of immunohistochemistry (IHC) for the "must-test" predictive biomarkers: anaplastic lymphoma kinase, ROS1, programmed cell death protein 1, and epidermal growth factor receptor. IHC using mutant-specific BRAF V600E, RET, pan-TRK, and LKB1 antibodies can be orthogonal tools for screening or confirmation of molecular events. ERBB2 and MET alterations include both activating mutations and gene amplifications, detection of which relies on molecular methods with a minimal role for IHC in NSCLC. IHC sits at the intersection of an integrated surgical pathology and molecular diagnostic practice, serves as a powerful functional surrogate for molecular testing, and is an indispensable tool of precision medicine in the care of lung cancer patients.

摘要

非小细胞肺癌(NSCLC)在全球范围内发病率和死亡率都很高,大多数患者在晚期被诊断出来,并越来越多地接受靶向治疗和免疫治疗。在这篇综述中,我们讨论了在外科病理学中最常见的肿瘤之一 NSCLC 中的诊断和预测性免疫组织化学标志物。我们强调了 2 个新兴的诊断标志物:用于 NUT 癌的睾丸核蛋白(NUT);用于 SMARCA4 缺陷性胸肿瘤的 SMARCA4。由于其具有高度侵袭性的行为,正确识别有助于实现最佳管理。对于晚期 NSCLC 患者,我们讨论了免疫组织化学(IHC)在“必须测试”的预测生物标志物中的实用性和局限性:间变性淋巴瘤激酶、ROS1、程序性死亡蛋白 1 和表皮生长因子受体。使用突变特异性 BRAF V600E、RET、泛 TRK 和 LKB1 抗体的 IHC 可以作为筛选或确认分子事件的正交工具。ERBB2 和 MET 改变包括激活突变和基因扩增,其检测依赖于分子方法,IHC 在 NSCLC 中的作用有限。IHC 位于综合外科病理学和分子诊断实践的交叉点,是分子检测的有力替代方法,也是肺癌患者精准医疗不可或缺的工具。

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