| Literature DB >> 34073635 |
Angela Santoro1, Giuseppe Angelico1, Antonio Travaglino1, Frediano Inzani1, Damiano Arciuolo1, Michele Valente1, Nicoletta D'Alessandris1, Giulia Scaglione1, Vincenzo Fiorentino1, Antonio Raffone2, Gian Franco Zannoni1,3.
Abstract
Endometrial carcinoma represents the most common gynecological cancer in Europe and the USA. Histopathological classification based on tumor morphology and tumor grade has played a crucial role in the management of endometrial carcinoma, allowing a prognostic stratification into distinct risk categories, and guiding surgical and adjuvant therapy. In 2013, The Cancer Genome Atlas (TCGA) Research Network reported a large scale molecular analysis of 373 endometrial carcinomas which demonstrated four categories with distinct clinical, pathologic, and molecular features: POLE/ultramutated (7% of cases) microsatellite instability (MSI)/hypermutated (28%), copy-number low/endometrioid (39%), and copy-number high/serous-like (26%). In the present article, we report a detailed histological and molecular review of all endometrial carcinoma histotypes in light of the current ESGO/ESTRO/ESP guidelines. In particular, we focus on the distribution and prognostic value of the TCGA groups in each histotype.Entities:
Keywords: CTNNB1; TCGA; clear cell carcinoma; endometrial carcinoma; prognosis; serous carcinoma; undifferentiated carcinoma
Year: 2021 PMID: 34073635 DOI: 10.3390/cancers13112623
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639