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The local management of soft tissue sarcoma
B O'Sullivan1, J Wylie, C Catton
1University Health Network, Princess Margaret Hospital, Toronto, Canada.
Seminars in Radiation Oncology
|October 12, 1999
Summary
Soft tissue sarcomas (STS) are rare connective tissue tumors. Effective management requires a multidisciplinary approach, with high local control rates achievable for extremity STS through modern treatments.
Area of Science:
- Oncology
- Surgical Oncology
- Radiotherapy
Background:
- Soft tissue sarcomas (STS) are rare, diverse tumors originating from connective tissues.
- STS management is challenging due to varied behavior, prognosis, and anatomic sites.
- Optimal treatment necessitates advanced diagnostic and therapeutic modalities.
Purpose of the Study:
- To outline the complexities and multidisciplinary approach required for soft tissue sarcoma management.
- To highlight the importance of specialized centers for improving patient outcomes.
- To discuss current treatment options and expected local control rates.
Main Methods:
- Review of diagnostic tools including pathology and imaging.
- Evaluation of treatment approaches: surgical ablation, reconstruction, radiotherapy, and chemotherapy.
- Emphasis on the multidisciplinary team setting for complex case management.
Main Results:
- Local control rates of at least 90% are achievable for the most common STS (extremity lesions) with modern strategies.
- Management of STS in other anatomic sites presents greater challenges, often due to late diagnosis and difficult access.
- Multidisciplinary care is crucial for successful outcomes, especially in complex or less common presentations.
Conclusions:
- Effective soft tissue sarcoma management relies on a comprehensive, multidisciplinary strategy.
- Referral to specialized sarcoma centers is vital for patients to maximize the chances of successful local outcome.
- Continued advancements in diagnostics and therapeutics are essential for improving STS patient care.

