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Updated: Feb 1, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Making the Best of Available Options for Optimal Sarcoma Treatment
1Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.
Abstract:
For 35 years options for treating advanced soft tissue sarcoma (STS) were limited to doxorubicin, dacarbazine and ifosfamide. In 2007, trabectedin was approved. Since then, several other agents have become available and many more are in development, ushering in a new era in disease management. Considerable scope exists for improving outcomes of advanced STS through better trial design and improved patient care in everyday practice. After anthracycline failure, there are a range of treatment options and, increasingly, the choice of therapy is histology driven. Introduction of newer agents and optimising use of established agents such as trabectedin has led to an increase in overall survival of advanced STS patients. Optimising treatment with trabectedin is being achieved through more extensive experience in drug management, mainly associated with use in earlier lines and uninterrupted use until disease progression. Identification by next-generation sequencing of a significant proportion of cases of actionable mutations among patients with advanced STS suggests a move towards matched therapy in future. As the armamentarium of active agents in advanced sarcoma increases, so too will the challenge of selecting the right drug for the right patient at the right time, in accordance with the patient's lifestyle and wishes.
Insights
Treatment options for advanced soft tissue sarcoma (STS) have expanded significantly since 2007. Optimizing therapies like trabectedin improves survival, with future treatments likely guided by genetic mutations.
Area of Science:
- Medical Oncology
- Sarcoma Research
- Pharmacology
Background:
- Advanced soft tissue sarcoma (STS) treatment was historically limited to a few chemotherapy agents for over 35 years.
- The approval of trabectedin in 2007 marked a turning point, initiating an evolving landscape of therapeutic options.
- Current management strategies are increasingly influenced by tumor histology and the availability of novel agents.
Purpose of the Study:
- To review the advancements in treating advanced soft tissue sarcoma (STS) over the past decades.
- To highlight the impact of newer agents and optimized use of established therapies on patient survival.
- To discuss the future direction of advanced STS treatment, including personalized medicine approaches.
Main Methods:
- Review of clinical trial data and treatment guidelines for advanced soft tissue sarcoma.
- Analysis of the evolving role of chemotherapy and targeted agents, including trabectedin.
- Exploration of the impact of next-generation sequencing in identifying actionable mutations.
Main Results:
- The introduction of newer agents and improved management of established drugs like trabectedin have increased overall survival for advanced STS patients.
- Optimized trabectedin use, including earlier lines of therapy and uninterrupted treatment, enhances outcomes.
- Next-generation sequencing reveals actionable mutations in a significant proportion of advanced STS cases.
Conclusions:
- The treatment paradigm for advanced STS has shifted towards a more diverse and histology-driven approach.
- Optimizing the use of existing therapies, such as trabectedin, remains crucial for improving patient outcomes.
- Future advanced STS treatment will likely involve personalized, mutation-matched therapies, requiring careful patient selection.
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