Systematic Review of Soft Tissue Sarcomas in Latin America.

IF 3.2 Q2 ONCOLOGY
JCO Global Oncology Pub Date : 2025-04-01 Epub Date: 2025-04-28 DOI:10.1200/GO-24-00508
Marlid Cruz-Ramos, Dorian Yarih García-Ortega, Renata Becerra-Herrera, Denise Carolina Cabello-Díaz, Sara Aileen Cabrera-Nieto, Gabriela A Martínez-Nava, Claudia Haydeé Saraí Caro-Sanchéz
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引用次数: 0

Abstract

Purpose: Soft tissue sarcomas (STSs) are rare malignant neoplasms posing significant public health challenges globally, especially in Latin America with limited research resources. This systematic review provides an overview of the epidemiology, clinical characteristics, treatment, and outcomes of STSs in Latin America, emphasizing the impact of insufficient investment in research and health care infrastructure.

Materials and methods: Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, we conducted a systematic literature review of clinicopathologic characteristics of STSs in Latin American patients. Studies published between January 1986 and August 2024 were included. A comprehensive search across multiple databases yielded 502 papers, refined to 18 publications and three national records included in the study. A meta-analysis was done for survival evaluation.

Results: Data from 2,931 patients with mean age 47 years were analyzed, and 340 patients had pretreatment biopsy. The most common sarcoma types were liposarcoma (23.2%) and synovial sarcoma (21.2%), with high-grade tumors (52%) predominating. Treatment primarily involved surgery (863 patients), often combined with radiotherapy (559 patients) and chemotherapy (307 patients). Five-year overall survival was 61%.

Discussion: The findings highlight challenges in managing STSs in Latin America, including advanced disease at diagnosis and high-grade tumors. Survival rates correlate with local advanced disease reported by other countries. Barriers include limited access to specialized centers and inadequate use of preoperative biopsies. Improved diagnostic and treatment strategies and collaborations to enhance research and clinical practices are needed.

Conclusion: This review underscores critical gaps in STS management in Latin America. Increased investment in research, a cohesive network of specialized care centers, and a multidisciplinary approach are essential to improve outcomes and quality of life for patients in the region.

拉丁美洲软组织肉瘤的系统综述。
目的:软组织肉瘤(STSs)是一种罕见的恶性肿瘤,在全球范围内构成了重大的公共卫生挑战,特别是在研究资源有限的拉丁美洲。本系统综述概述了拉丁美洲性传播感染的流行病学、临床特征、治疗和结果,强调了研究和卫生保健基础设施投资不足的影响。材料和方法:根据系统评价和荟萃分析指南的首选报告项目,我们对拉丁美洲患者的STSs临床病理特征进行了系统的文献回顾。1986年1月至2024年8月期间发表的研究被纳入其中。在多个数据库中进行的全面搜索产生了502篇论文,其中包括18篇出版物和3篇国家记录。对生存评估进行荟萃分析。结果:分析了2931例患者的数据,平均年龄为47岁,340例患者进行了预处理活检。最常见的肉瘤类型为脂肪肉瘤(23.2%)和滑膜肉瘤(21.2%),以高级别肿瘤(52%)为主。治疗主要包括手术(863例),通常联合放疗(559例)和化疗(307例)。5年总生存率为61%。讨论:研究结果突出了拉丁美洲管理STSs的挑战,包括诊断时的晚期疾病和高级别肿瘤。存活率与其他国家报告的当地晚期疾病相关。障碍包括进入专门中心的机会有限和术前活检的使用不足。需要改进诊断和治疗战略以及加强研究和临床实践的合作。结论:本综述强调了拉丁美洲STS管理的关键差距。增加对研究的投资,建立一个有凝聚力的专业护理中心网络,以及采用多学科方法,对于改善该地区患者的预后和生活质量至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JCO Global Oncology
JCO Global Oncology Medicine-Oncology
CiteScore
6.70
自引率
6.70%
发文量
310
审稿时长
7 weeks
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