Characteristics and Outcomes of Soft Tissue Sarcoma in Saudi Arabia: A 10-Year Experience.

IF 2.6 4区 医学 Q3 ONCOLOGY
Cancer Management and Research Pub Date : 2025-09-16 eCollection Date: 2025-01-01 DOI:10.2147/CMAR.S530633
Bader Alshamsan, Omar I Alrifai, Mohammad A Altayeb, Mohammed M Alobud, Aiman Alshomrani, Nouf F Alsadoun, Rashed Bin Khidhr, Rajeev Pant, Mahmood Shaheen, Jean Paul Atallah
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引用次数: 0

Abstract

Purpose: Soft tissue sarcomas (STS) are rare, heterogeneous malignancies representing less than 1% of solid cancers. Given the diversity of subtypes and the complexity of management, understanding regional epidemiological patterns is essential. This study aimed to evaluate the clinical characteristics, treatment strategies, and prognostic factors in STS patients in Saudi Arabia at a sarcoma center.

Patients and methods: This retrospective study included 214 patients with STS treated between 2010 and 2020. Patient demographics, tumor characteristics, clinical stage, and treatment modalities were collected using REDCap. Overall survival (OS) was estimated using Kaplan-Meier curves, and prognostic factors were analyzed using Cox regression. Statistical significance was set at p < 0.05.

Results: The median age at diagnosis was 37 years (IQR: 25-49.5), and the median symptom duration before diagnosis was 8 months. Synovial sarcoma (20%) was the most common subtype, followed by liposarcoma (13.6%) and undifferentiated pleomorphic sarcoma (12%). Metastatic disease at diagnosis was reported in 39% of patients, with the lower limb being the most affected site (62.1%). Local treatment included surgery alone (45.3%), radiation alone (7.5%), and combined surgery and radiation (41.6%). Median OS was not reached in localized disease, whereas it was 26 months in metastatic cases (p< 0.01). Age ≥65 years (hazard ratio[HR]: 6.05, p=0.002), larger tumor size (HR: 9.12, p=0.04), and metastasis (HR: 8.77, p<0.001) were associated with worse survival. Tumors in extremities (HR: 0.38, p=0.04) and combined local therapy (HR: 0.13, p=0.009) were associated with better OS. Multimodal therapy improved OS in metastatic cases (p=0.004).

Conclusion: STS in Saudi Arabia presents at a younger age, with prolonged symptom duration, and a high burden of metastatic disease. Despite these challenges, outcomes are comparable to global trends, particularly multimodal approaches. Future research should identify barriers to early diagnosis, improve healthcare access, and explore novel systemic therapies.

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沙特阿拉伯软组织肉瘤的特点和预后:10年经验
目的:软组织肉瘤(STS)是一种罕见的异质性恶性肿瘤,占实体癌的不到1%。鉴于亚型的多样性和管理的复杂性,了解区域流行病学模式至关重要。本研究旨在评估沙特阿拉伯肉瘤中心STS患者的临床特征、治疗策略和预后因素。患者和方法:本回顾性研究纳入了2010年至2020年间接受STS治疗的214例患者。使用REDCap收集患者人口统计学、肿瘤特征、临床分期和治疗方式。采用Kaplan-Meier曲线估计总生存期(OS),采用Cox回归分析预后因素。p < 0.05为差异有统计学意义。结果:诊断时中位年龄37岁(IQR: 25-49.5),诊断前中位症状持续时间为8个月。滑膜肉瘤(20%)是最常见的亚型,其次是脂肪肉瘤(13.6%)和未分化多形性肉瘤(12%)。39%的患者诊断时有转移性疾病,其中下肢是最受影响的部位(62.1%)。局部治疗包括单纯手术(45.3%)、单纯放疗(7.5%)和手术加放疗(41.6%)。局部疾病的中位生存期未达到,而转移病例的中位生存期为26个月(p< 0.01)。年龄≥65岁(危险比[HR]: 6.05, p=0.002)、肿瘤较大(危险比[HR]: 9.12, p=0.04)、转移(危险比:8.77)。结论:沙特阿拉伯STS患者发病年龄较轻,症状持续时间较长,转移负担高。尽管存在这些挑战,但结果可与全球趋势相媲美,特别是多式联运方法。未来的研究应该确定早期诊断的障碍,改善医疗服务的可及性,并探索新的全身治疗方法。
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来源期刊
Cancer Management and Research
Cancer Management and Research Medicine-Oncology
CiteScore
7.40
自引率
0.00%
发文量
448
审稿时长
16 weeks
期刊介绍: Cancer Management and Research is an international, peer reviewed, open access journal focusing on cancer research and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for cancer patients. Specific topics covered in the journal include: ◦Epidemiology, detection and screening ◦Cellular research and biomarkers ◦Identification of biotargets and agents with novel mechanisms of action ◦Optimal clinical use of existing anticancer agents, including combination therapies ◦Radiation and surgery ◦Palliative care ◦Patient adherence, quality of life, satisfaction The journal welcomes submitted papers covering original research, basic science, clinical & epidemiological studies, reviews & evaluations, guidelines, expert opinion and commentary, and case series that shed novel insights on a disease or disease subtype.
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