4.7 Review

Clinical actionability of molecular targets in endometrial cancer

Journal

NATURE REVIEWS CANCER
Volume 19, Issue 9, Pages 510-521

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41568-019-0177-x

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Funding

  1. Intramural Research Program of the National Human Genome Research Institute at NIH [HG200338, HG200379]
  2. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [ZIAHG200379, ZIAHG200338] Funding Source: NIH RePORTER

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Endometrial cancer accounts for similar to 76,000 deaths among women each year worldwide. Disease mortality and the increasing number of new diagnoses make endometrial cancer an important consideration in women's health, particularly in industrialized countries, where the incidence of this tumour type is highest. Most endometrial cancers are carcinomas, with the remainder being sarcomas. Endometrial carcinomas can be classified into several histological subtypes, including endometrioid, serous and clear cell carcinomas. Histological subtyping is currently used routinely to guide prognosis and treatment decisions for endometrial cancer patients, while ongoing studies are evaluating the potential clinical utility of molecular subtyping. In this Review, we summarize the overarching molecular features of endometrial cancers and highlight recent studies assessing the potential clinical utility of specific molecular features for early detection, disease risk stratification and directing targeted therapies.

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