Abstract

Objective:To determine the clinical and pathologic characteristics, prognostic factors, surgical practice, adjuvant therapies, and survival outcomes of patients with uterine sarcoma diagnosed and treated in our institution.Material and Methods:Patients diagnosed and treated for uterine sarcomas at our institution from 2009 to 2017 were retrospectively evaluated. All histologic slides from the specimens underwent a thorough pathologic review by a gynecologic pathologist. The following variables were assessed: age, family history of cancer, smoking status, age of menarche, parity, age at first delivery, related symptoms, clinical staging, histologic type, treatment received, disease-free period, and the time and site of recurrence, as well as treatment of the latter and overall survival.Results:Ten patients were diagnosed as having leiomyosarcoma, a further 10 patients had malignant mixed mullerian tumors, and five had endometrial stromal sarcoma; the remaining nine patients had other tumors. At the end of our study, 12 (35.3%) patients were alive and in remission, four (11.8%) were alive with disease, 10 (29.4%) were lost to follow-up, and eight (23.5%) had died. The mean survival time was 80.92 months, and the 2-year survival rate was 75.6%. We found that survival was significantly shorter in the presence of lymph node involvement, residual tumor, and recurrence.Conclusion:This study serves to inform physicians about the outcome of various uterine sarcomas that were diagnosed and managed at our center. We found that 35.3% of our patients were alive and in remission, 11.8% were alive with disease, 29.4% were lost to follow-up, and 23.5% of patients died.

Highlights

  • IntroductionUterine sarcomas are malignant tumors that originate from the mesodermal tissues (muscle and supportive tissues) of the uterus

  • Uterine sarcomas are malignant tumors that originate from the mesodermal tissues of the uterus

  • Our patient group included those who had been diagnosed as having uterine carcinosarcomas [ called malignant mixed mullerian tumors (MMMT)] because these tumors are classified within the uterine carcinoma group, having previously been considered as uterine sarcomas [14,15]

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Summary

Introduction

Uterine sarcomas are malignant tumors that originate from the mesodermal tissues (muscle and supportive tissues) of the uterus. They are usually of heterogeneous characteristics and represent a small group among the malignant neoplasms of the uterus [1,2]. The World Health Organization (WHO) classifies uterine sarcomas into two types: [1] malignant mesenchymal tumors, and [2] mixed epithelial and mesenchymal tumors. Pure mesenchymal tumors are further subclassified as leiomyosarcoma (LMS), low- and high-grade endometrial stromal sarcomas (LG-ESS and HG-ESS, respectively) and undifferentiated uterine sarcoma (UUS) [4]. Mixed tumors comprise adenosarcoma (AS), rhabdomyosarcoma (RMS), and perivascular epithelioid cell

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