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As of 2022, approximately 172,585 individuals in the United States were living with soft tissue sarcoma (STS), according to SEER. Despite its rarity, with an incidence rate of 3.5 per 100,000, the five-year survival rate stands at 66%, reflecting significant survival rates. The associated mortality rate of 1.3 per 100,000 highlights the need for early detection and effective treatment strategies to reduce disease burden and improve outcomes.
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Expert Market Research's “Soft Tissue Sarcoma Epidemiology Forecast Report 2026-2035” offers comprehensive information on the prevalence and demographics of soft tissue sarcoma. It projects the future incidence and prevalence rates of soft tissue sarcoma cases across various populations. The study covers age, gender, and type as major determinants of the soft tissue sarcoma population. The report highlights patterns in the prevalence of soft tissue sarcoma over time and projects future trends based on multiple variables.
The report provides a comprehensive overview of the disease, as well as historical and projected data on the epidemiology of soft tissue sarcoma in the 8 major markets.
Regions Covered
Soft tissue sarcoma (STS) is a diverse group of malignant tumors arising from mesenchymal tissues such as fat, muscle, nerves, and blood vessels. Over 50 histological subtypes exist, with leiomyosarcoma, liposarcoma, and undifferentiated pleomorphic sarcoma among the most prevalent. These tumors can occur in any part of the body, but the extremities are most frequently affected. Although STS can develop at any age, incidence increases with advancing age and is slightly more common in males. Delayed diagnosis is frequent due to nonspecific symptoms and the tumor’s deep-seated growth.
The soft tissue sarcoma epidemiology division offers information on the patient pool from history to the present as well as the projected trend for each of the 8 major markets. Expert Market Research provides both current and predicted trends for soft tissue sarcoma epidemiology scenario by examining a wide range of studies. Additionally, the report covers the diagnosed patient pool for soft tissue sarcoma and their trends. The soft tissue sarcoma detailed epidemiology segmentation is broken down into specific categories, such as total prevalent cases in males and females, and total diagnosed cases across different age groups and patient pools.

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The soft tissue sarcoma epidemiology data and findings for the United States, Germany, Spain, Italy, France, the United Kingdom, Japan, and India are also provided in the epidemiology section.
The epidemiological outlook for soft tissue sarcoma (STS) reveals varying trends across age groups, geographies, and subtypes. In the United States, soft tissue sarcoma (STS) remains a rare cancer, accounting for less than 1% of all adult malignancies, with incidence increasing with age and more common in men, as noted by the American Cancer Society. A retrospective study in India found a predominance of STS among males, especially in the lower limbs, and in the 41-50 age group. Meanwhile, in the United Kingdom, the five-year survival rate ranges from 55% to 60%, largely dependent on the histologic subtype, tumor size, and stage at diagnosis, with earlier detection associated with better prognosis. These regional patterns underscore the heterogeneity of soft tissue sarcoma presentation and outcomes, emphasizing the need for context-specific strategies in diagnosis, treatment, and long-term management.
The treatment of soft tissue sarcoma (STS) relies on a multidisciplinary approach involving surgery, radiation therapy, and systemic therapies. Limb-sparing surgeries are now standard in specialized centers, often combined with radiotherapy to improve local control. Chemotherapy, typically involving doxorubicin-based regimens, is considered for high-grade or metastatic cases, while targeted therapies such as pazopanib and investigational agents are used in specific subtypes. Advances in molecular diagnostics have also allowed precision medicine approaches, particularly in recurrent or treatment-resistant tumors, improving treatment personalization and offering better outcomes for patients with rare histologic variants.
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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Base Year |
2025 |
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Historical Period |
2019-2025 |
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Forecast Period |
2026-2035 |
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Epidemiology Statistics Provided |
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