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Updated: Jan 26, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
The challenge of finding new therapeutic avenues in soft tissue sarcomas
1Sarcoma Unit, Interdisciplinary Tumor Center Mannheim, Mannheim University Medical Center, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Abstract:
Soft tissue sarcomas are rare malignancies of mesenchymal origin comprising about 1% of all adult cancers. Systemic therapies for locally advanced and metastatic disease have been restricted for decades to very few effective and approved agents such as doxorubicin and ifosfamide. However, new therapeutic avenues including new drug developments and registrations such as trabectedin, pazopanib and eribulin as well as numerous clinical trial options have recently enriched the therapeutic armamentarium in the treatment of patients with advanced soft tissue sarcomas. The challenges and pitfalls of finding such new therapeutic avenues in recent years for the treatment benefit of patients with soft tissue sarcomas will be presented in this chapter within the thematic series on "Challenges in Sarcoma".
Insights
Soft tissue sarcomas, rare cancers, have limited treatment options. Recent advancements offer new drugs and clinical trials, expanding therapeutic choices for advanced disease.
Area of Science:
- Oncology
- Medical Oncology
- Sarcoma Research
Background:
- Soft tissue sarcomas (STS) are rare mesenchymal malignancies, representing approximately 1% of adult cancers.
- Systemic treatment for advanced or metastatic STS has historically relied on a limited number of agents, primarily doxorubicin and ifosfamide.
- The therapeutic landscape for STS has seen recent expansion, offering new hope for patients.
Purpose of the Study:
- To review the recent advancements in systemic therapies for advanced and metastatic soft tissue sarcomas.
- To discuss the challenges and pitfalls encountered in developing and registering new therapeutic options for STS.
- To highlight the enriched therapeutic armamentarium available for patients with advanced soft tissue sarcomas.
Main Methods:
- Literature review of recent clinical trials and drug approvals for soft tissue sarcomas.
- Analysis of systemic therapy options for locally advanced and metastatic disease.
- Discussion of challenges in drug development and clinical trial design for rare cancers.
Main Results:
- Several new agents, including trabectedin, pazopanib, and eribulin, have been approved for advanced STS.
- Numerous clinical trial options are now available, significantly increasing treatment choices.
- The availability of new therapies marks a significant improvement over the previously restricted options.
Conclusions:
- The treatment of advanced soft tissue sarcomas has significantly evolved with the introduction of new drugs and clinical trials.
- Despite progress, challenges remain in optimizing treatment strategies and access to novel therapies.
- Continued research and clinical investigation are crucial for further improving outcomes in soft tissue sarcoma patients.
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