How do different histologic components of mixed endometrial carcinomas affect prognosis? Does it really matter?

Author:

Thomakos Nikolaos1ORCID,Dimopoulou Stefania1,Sotiropoulou Maria2,Machairiotis Nikolaos3,Pandraklakis Anastasios1,Haidopoulos Dimitrios1,Liontos Michalis4,Bamias Aristotelis4,Rodolakis Alexandros1

Affiliation:

1. 1st Department of Obstetrics and Gynecology , Alexandra Hospital, Gynecologic Oncology Unit, University of Athens , Athens , Greece

2. Department of Obstetrics and Gynecology , Royal Surrey County Hospital , Surrey , UK

3. Department of Pathology , Alexandra Hospital , Athens , Greece

4. Department of Clinical Therapeutics , Oncology Unit, National and Kapodistrian Unviersity of Athens, Alexandra Hospital , Athens , Greece

Abstract

Abstract The aim of this study is to evaluate and compare outcomes of patients with mixed and pure endometrial carcinomas (MEC). We reviewed data of patients with MEC, endometroid (EC), serous (SC), and clear cell (CC) carcinomas between 2002 and 2015. Overall survival (OS) and disease-free (DF) survival rates were evaluated, according to the percentage of histologic components. Clinicopathological variables and treatment strategies were assessed. Furthermore, χ 2 tests were used to compare proportions and Kaplan–Meier curves to compare recurrence and survival. Sample consisted of 302 cases with mean age 66.3 years. Early-stage disease was recorded in EC compared with CC and SC. Adnexal involvement was more frequent in MEC compared with EC (p=0.043). Extra uterine metastasis was more frequent in the SC compared to the EC group, while lymphovascular space involvement was more frequent in the MEC and CC compared to the SC (p=0.001). EC had less omentum involvement compared to CC (p=0.035) and SC (p<0.001). Furthermore, cervical involvement was more frequent in CC compared to EC (p=0.011). Recurrence (p=0.265) and OS (p=0.533) were found to be similar in MEC compared with CC, SC, and EC. Moreover, recurrence and OS were similar between EC-CC and EC-SC. There were no differences in recurrence and survival in MEC with a type II component larger than 10% or 20% (p>0.05).

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Molecular Biology,General Medicine,Endocrinology, Diabetes and Metabolism

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