Department of Obstetrics and Gynaecology, The University of British Colombia, Vancouver, Canada.
Department of Pathology, Leiden University Medical Centre (LUMC), Leiden, The Netherlands.
J Pathol. 2018 Apr;244(5):538-549. doi: 10.1002/path.5034. Epub 2018 Feb 28.
Endometrial cancer is a clinically heterogeneous disease and it is becoming increasingly clear that this heterogeneity may be a function of the diversity of the underlying molecular alterations. Recent large-scale genomic studies have revealed that endometrial cancer can be divided into at least four distinct molecular subtypes, with well-described underlying genomic aberrations. These subtypes can be reliably delineated and carry significant prognostic as well as predictive information; embracing and incorporating them into clinical practice is thus attractive. The road towards the integration of molecular features into current classification systems is not without obstacles. Collaborative studies engaging research teams from across the world are working to define pragmatic assays, improve risk stratification systems by combining molecular features and traditional clinicopathological parameters, and determine how molecular classification can be optimally utilized to direct patient care. Pathologists and clinicians caring for women with endometrial cancer need to engage with and understand the possibilities and limitations of this new approach, because integration of molecular classification of endometrial cancers is anticipated to become an essential part of gynaecological pathology practice. This review will describe the challenges in current systems of endometrial carcinoma classification, the evolution of new molecular technologies that define prognostically distinct molecular subtypes, and potential applications of molecular classification as a step towards precision medicine and refining care for individuals with the most common gynaecological cancer in the developed world. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
子宫内膜癌是一种临床异质性疾病,越来越明显的是,这种异质性可能是潜在分子改变多样性的一种功能。最近的大规模基因组研究表明,子宫内膜癌至少可以分为四个不同的分子亚型,具有明确的潜在基因组异常。这些亚型可以可靠地区分,并具有显著的预后和预测信息;因此,将它们纳入临床实践是很有吸引力的。将分子特征纳入当前分类系统的道路并非没有障碍。来自世界各地的研究团队正在进行合作研究,旨在定义实用的检测方法,通过结合分子特征和传统临床病理参数来改善风险分层系统,并确定如何最佳利用分子分类来指导患者治疗。为子宫内膜癌患者提供护理的病理学家和临床医生需要参与并了解这种新方法的可能性和局限性,因为预计将子宫内膜癌的分子分类纳入妇科病理学实践将成为一个重要组成部分。这篇综述将描述当前子宫内膜癌分类系统中的挑战,以及定义预后不同的分子亚型的新分子技术的发展,以及作为迈向精准医学和为发达国家最常见妇科癌症患者提供更精细护理的一步,分子分类的潜在应用。版权所有©2018 英国和爱尔兰病理学学会。由 John Wiley & Sons,Ltd. 出版。