Histopathological features of endometrial carcinomas associated with POLE mutations: Implications for decisions about adjuvant therapy Journal Article


Authors: Bakhsh, S.; Kinloch, M.; Hoang, L. N.; Soslow, R. A.; Köbel, M.; Lee, C. H.; McAlpine, J. N.; McConechy, M. K.; Gilks, C. B.
Article Title: Histopathological features of endometrial carcinomas associated with POLE mutations: Implications for decisions about adjuvant therapy
Abstract: Aims: To characterize the histomorphological features of endometrial carcinomas (ECs) harbouring polymerase epsilon (POLE) mutations. Methods and results: Forty-three ECs with POLE mutations were compared with a cohort of 202 ECs. Most POLE-mutated ECs were endometrioid [34/43 (79%)]; the remaining tumours were mixed [6/43 (14%)], serous [2/43 (5%)], and clear cell [1/43 (2%)]. The endometrioid carcinomas were predominantly International Federation of Gynecology and Obstetrics grade 3 (27/43, 63%). The histotype distribution did not differ from that of control ECs (P = 0.69), but the grade of the EC was higher (P < 0.0005). Both nuclear grade and mitotic index were significantly higher in POLE-mutated ECs than in the comparison cohort. POLE-mutated ECs were associated with peritumoral lymphocytes and numerous tumour-infiltrating lymphocytes. Lymphovascular invasion was present in 20 of 43 tumours. Adjuvant radiotherapy and adjuvant chemotherapy would be offered in up to 80% and 40% of patients, respectively, on the basis of stage, grade, lymphovascular invasion, and histotype. Conclusions: POLE-mutated ECs are typically of high grade, with prominent lymphocytic infiltration, but they are not sufficiently distinctive to allow accurate diagnosis based on routine haematoxylin and eosin staining. Even though POLE-mutated tumours are associated with an excellent prognosis, current guidelines for giving adjuvant treatment for EC result in most patients receiving adjuvant therapy.
Keywords: immunohistochemistry; classification; endometrial carcinoma; mutations; polymerase; tcga; cancer; pole; exonuclease domain mutations
Journal Title: Histopathology
Volume: 68
Issue: 6
ISSN: 0309-0167
Publisher: Wiley Blackwell  
Date Published: 2016-05-01
Start Page: 916
End Page: 924
Language: English
ACCESSION: WOS:000374553600016
DOI: 10.1111/his.12878
PROVIDER: wos
PUBMED: 26416160
PMCID: PMC5650229
Notes: Article -- Source: Wos
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  1. Robert Soslow
    793 Soslow