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Updated: Jul 10, 2025

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A Mouse Model of Incompletely Resected Soft Tissue Sarcoma for Testing Neoadjuvant Therapies
Published on: July 28, 2020
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Retroperitoneal Soft Tissue Sarcoma: Emerging Therapeutic Strategies
Eelco de Bree1, Dimosthenis Michelakis1, Ioannis Heretis2
1Department of Surgical Oncology, Medical School of Crete University Hospital, 71110 Heraklion, Greece.
Cancers
|November 25, 2023
Summary
Retroperitoneal soft tissue sarcoma (RPS) management requires tailored, multidisciplinary approaches. Personalized treatment based on histology and grade improves outcomes, moving beyond one-size-fits-all strategies for this rare cancer.
Area of Science:
- Oncology
- Surgical Oncology
- Radiotherapy
Background:
- Retroperitoneal soft tissue sarcoma (RPS) presents unique challenges due to its location, size, and indistinct borders, leading to high local recurrence rates.
- Local recurrence is a primary cause of mortality in low-grade RPS, while high-grade tumors often metastasize distantly.
Purpose of the Study:
- To comprehensively review recent data on the evolving multidisciplinary management of primary localized RPS.
- To discuss the impact of emerging therapeutic strategies on oncological outcomes.
Main Methods:
- Review of recent literature on multidisciplinary management of primary localized RPS.
- Analysis of data regarding extended surgery, neoadjuvant/adjuvant treatments, and radiotherapy.
Main Results:
- Extended surgery with compartmental resection improves local control in low-grade RPS and liposarcoma, but not leiomyosarcoma.
- Preoperative radiotherapy may benefit specific subtypes like well-differentiated liposarcoma and solitary fibrous tumors.
- The benefit of neoadjuvant chemotherapy for high-grade RPS is still under investigation.
Conclusions:
- A personalized, histology-tailored multimodality treatment approach is crucial for improving RPS management.
- Future strategies will likely incorporate a deeper understanding of RPS molecular and genetic characteristics.

