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首页> 外文期刊>Virchows Archiv: an international journal of pathology >Mutational Screening of BRCA1/2 Genes as a Predictive Factor for Therapeutic Response in Epithelial Ovarian Cancer: A Consensus Guide from the Spanish Society of Pathology (SEAP-IAP) and the Spanish Society of Human Genetics (AEGH)
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Mutational Screening of BRCA1/2 Genes as a Predictive Factor for Therapeutic Response in Epithelial Ovarian Cancer: A Consensus Guide from the Spanish Society of Pathology (SEAP-IAP) and the Spanish Society of Human Genetics (AEGH)

机译:BRCA1 / 2基因的突变筛选作为上皮性卵巢癌治疗反应的预测因素:来自西班牙病理学学会(SEAP-IAP)和人类遗传学学会(AEGH)的共识指南

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摘要

Germline/somatic BRCA-mutated ovarian carcinomas (OC) are associated to have better response with platinum-based chemotherapy and long-term prognosis than non-BRCA-associated OCs. In addition, these mutations are predictive factors to response to Poly(ADP-ribose) polymerase (PARP) inhibitors. Different positioning papers have addressed the clinical recommendations for BRCA testing in OC. This consensus guide represents a collection of technical recommendations to address the detection of BRCA1/2 mutations in the molecular diagnostic testing strategy for OC. Under the coordination of Spanish Society of Pathology (SEAP-IAP) and the Spanish Society of Human Genetics (AEGH), these recommendations have been developed by pathologists and geneticists taking into account previously published recommendations and their experience in the molecular characterization of these genes. Since the implementation of BRCA testing as a predictive factor can initiate the workflow by testing germline mutations in the blood or by testing both germline and somatic mutations in tumor tissue, distinctive features of both strategies are discussed. Additionally, the recommendations included in this paper provide some references, quality parameters, and genomic tools aimed to standardize and facilitate the clinical genomic diagnosis of OC.
机译:种系/体细胞BRCA-突变的卵巢癌(OC)与铂类化疗和长期预后的卵巢癌(OC)相关,而不是非BRCA相关的OC。此外,这些突变是对聚(ADP-核糖)聚合酶(PARP)抑制剂的反应的预测因素。不同的定位文件已经解决了在OC中的BRCA测试的临床推荐。本共识指南代表了一种技术建议,以解决OC的分子诊断检测策略中BRCA1 / 2突变的检测。根据西班牙病理学会(SEAP-IAP)和人类遗传学协会(AEGH)的协调,通过病理学家和遗传学家制定了这些建议,考虑到以前公布的建议及其在这些基因分子表征中的经验。由于BRCA测试作为预测因子的实施可以通过测试血液中的种类突变或通过测试肿瘤组织中的种系和体细胞突变,讨论两种策略的独特特征,因此可以启动工作流程。此外,本文中包含的建议提供了一些参考,质量参数和基因组工具,旨在标准化和促进OC的临床基因组诊断。

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