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Updated: May 13, 2026

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A Mouse Model of Incompletely Resected Soft Tissue Sarcoma for Testing (Neo)adjuvant Therapies
Published on: July 28, 2020
Pazopanib, a new therapy for metastatic soft tissue sarcoma
Jaap Verweij1, Stefan Sleijfer
1Erasmus MC Cancer Institute, Department of Medical Oncology, ' s-Gravendijkwal 230, Room He-116, 3015 CE Rotterdam, The Netherlands. j.verweij@erasmusmc.nl
Expert Opinion on Pharmacotherapy
|March 16, 2013
Summary
Pazopanib significantly improves progression-free survival in patients with advanced soft tissue sarcomas. This vascular endothelial growth factor receptor inhibitor offers a manageable safety profile, establishing it as a standard care option.
Area of Science:
- Oncology
- Pharmacology
- Angiogenesis Inhibition
Background:
- Pazopanib is a multi-tyrosine kinase inhibitor targeting vascular endothelial growth factor receptors.
- It inhibits the angiogenesis pathway, crucial for tumor growth.
- Soft tissue sarcomas represent a group of diseases with significant unmet medical needs.
Purpose of the Study:
- To review the role of angiogenesis in soft tissue sarcomas.
- To summarize the clinical pharmacology of pazopanib.
- To evaluate the efficacy and safety of pazopanib in soft tissue sarcoma treatment.
Main Methods:
- Review of preclinical and clinical data, including Phase I, II, and III studies.
- Focus on randomized, placebo-controlled Phase III trial.
- Analysis of progression-free survival and safety profile.
Main Results:
- Pazopanib demonstrated significant activity in chemotherapy-failing nonadipocytic soft tissue sarcomas.
- Progression-free survival nearly tripled, from 1.6 to 4.6 months.
- The drug exhibited a manageable safety profile with high dose intensity.
Conclusions:
- Pazopanib is an effective treatment for advanced soft tissue sarcomas.
- It represents a valuable addition to the standard of care for this patient population.
- The drug offers a significant survival benefit with acceptable toxicity.
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