Soft Tissue Sarcomas: Epidemiological, Clinical and Therapeutic Aspects

Mehdi Raouah, Ahmed Anis Agouzzal, Mouna Darfaoui, Issam Lalya, Abdelhamid El Omrani, Mouna Khouchani
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Abstract

Soft-tissue sarcomas (STS) are a rare, and comprise a relatively heterogeneous group of malignant tumors arising from mesenchymal tissue. STS can affect any age group. In order to provide patients suffering from STS, with a functional extremity without local tumor relapse, treatment decisions must involve a multidisciplinary team decision-making approach. We conducted a retrospective, descriptive study, of 43 cases of soft tissue sarcoma, collected between January 2013 and December 2018, in the department of Radiation-Oncology of the Oncology and hematology hospital of Mohammed VI University Teaching Hospital. With this study we aimed to report the epidemiological, clinical, histological, therapeutic and evolutionary characteristics of soft tissue sarcomas in the Radiation-Oncology department, and to define the factors influencing patient survival in order to improve the quality of care. The items collected were: epidemiological, clinical, histological, radiological, and therapeutic. Univariate and then multivariate analyzes were performed looking for factors influencing 2-year survival. During the study period, we collected 43 cases, 22 Men and 21 Women, the average age was 45.23 years (Extreme = 11-78 years). The tumor was deep in 73% percent of the cases, and the lower limbs were the most affected (65%) especially in the thigh. The predominant histological type was Liposarcoma in 16 cases (37.20%). The tumor stage was localized in 35 cases (81.39%), metastatic in 8 cases (18.60%). Thirty-five tumors were treated with surgery, including 31 cases (88.57%) of conservative surgery and 4 cases (11.42%) of radical surgery. Radiotherapy was performed in 33 patients, and chemotherapy in 24 patients. Follow-up monitoring has detected 5 cases (28%) of local recurrence, and 13 other cases (72%) of distant metastases. In univariate analysis the prognostic factors were age (p = 0.03) and tumor stage (p = 0.09). In our study, radiation therapy is an integral part of the ......
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软组织肉瘤:流行病学、临床和治疗方面
软组织肉瘤(STS)是一种罕见的,由一组相对异质性的恶性肿瘤引起的间质组织。STS可影响任何年龄组。为了保证STS患者肢体功能正常且没有局部肿瘤复发,治疗决策必须涉及多学科团队决策方法。我们对2013年1月至2018年12月在穆罕默德六世大学教学医院肿瘤学和血液学医院放射肿瘤科收集的43例软组织肉瘤进行了回顾性描述性研究。本研究旨在报告放射肿瘤科软组织肉瘤的流行病学、临床、组织学、治疗和进化特征,并确定影响患者生存的因素,以提高护理质量。收集的项目包括:流行病学、临床、组织学、放射学和治疗学。分别进行单因素和多因素分析,寻找影响2年生存率的因素。研究期间共收集43例患者,男22例,女21例,平均年龄45.23岁(极值= 11 ~ 78岁)。73%的病例肿瘤位于深部,下肢受影响最大(65%),尤其是大腿。16例(37.20%)以脂肪肉瘤为主。肿瘤分期局限35例(81.39%),转移8例(18.60%)。手术治疗35例肿瘤,其中保守手术31例(88.57%),根治性手术4例(11.42%)。放疗33例,化疗24例。随访监测发现局部复发5例(28%),远处转移13例(72%)。单因素分析中影响预后的因素为年龄(p = 0.03)和肿瘤分期(p = 0.09)。在我们的研究中,放射治疗是......的一个组成部分
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