1. New pathological and clinical insights in endometrial cancer in view of the updated esgo/estro/esp guidelines
- Author
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Santoro, Angela, Angelico, G., Travaglino, A., Inzani, Frediano, Arciuolo, Damiano, Valente, Marianna, D'Alessandris, N., Scaglione, G., Fiorentino, V., Raffone, A., Zannoni, Gian Franco, Santoro A. (ORCID:0000-0002-6964-5152), Inzani F., Arciuolo D., Valente M., Zannoni G. F. (ORCID:0000-0003-1809-129X), Santoro, Angela, Angelico, G., Travaglino, A., Inzani, Frediano, Arciuolo, Damiano, Valente, Marianna, D'Alessandris, N., Scaglione, G., Fiorentino, V., Raffone, A., Zannoni, Gian Franco, Santoro A. (ORCID:0000-0002-6964-5152), Inzani F., Arciuolo D., Valente M., and Zannoni G. F. (ORCID:0000-0003-1809-129X)
- 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 fea-tures: 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.
- Published
- 2021