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Updated: Feb 2, 2026

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Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
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Clear cell sarcoma : a retrospective review from a tertiary orthopaedic sarcoma unit
Natalie Green1, James E Archer1, Charles A E Baird1
1Royal Orthopaedic Hospital, Birmingham, UK.
The Bone & Joint Journal
|January 31, 2026
Summary
Clear cell sarcoma has a modest survival rate, with 37.4% of patients surviving at ten years. Early detection of metastases with PET CT aids treatment, and complete surgical excision offers the best chance for cure.
Area of Science:
- Oncology
- Orthopedic Surgery
- Soft Tissue Tumors
Background:
- Clear cell sarcoma is an aggressive soft tissue malignancy.
- Optimal management strategies require further investigation.
- Understanding prognostic factors is crucial for patient outcomes.
Purpose of the Study:
- To evaluate the presentation, investigation, and management of clear cell sarcoma.
- To report survival rates, local recurrence, and metastasis development.
- To identify factors influencing patient outcomes.
Main Methods:
- Retrospective review of a prospectively maintained oncology database.
- Inclusion of 47 patients treated between January 1996 and January 2024.
- Median follow-up of 28 months, assessing survival, local recurrence, and metastases.
Main Results:
- Overall survival was 37.4% at ten years; median survival was 40 months.
- Metastases were present at diagnosis in 28% of patients, identified effectively with PET CT.
- Local recurrence occurred in 19%, and metastases in 43%; complete excision with disease-free margins improved cure rates.
Conclusions:
- Clear cell sarcoma exhibits aggressive behavior with modest survival rates.
- Early metastasis detection via PET CT enhances treatment focus.
- Future research should explore targeted immunotherapies to improve outcomes.
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