Related Experiment Video
Updated: Jun 25, 2026

Percutaneous Hepatic Perfusion PHP with Melphalan as a Treatment for Unresectable Metastases Confined to the Liver
Published on: July 31, 2016
Real-world experience with pazopanib in locally advanced and metastatic soft tissue sarcomas: a Hungarian
Nóra Ecker1, Marietta Aranyi1, Edina Kiss1
1Department of Medical Oncology, Central Hospital of Northern Pest-Military Hospital, Budapest, Hungary.
Abstract:
Pazopanib is a tyrosine-kinase inhibitor also used for the treatment of advanced soft tissue sarcomas. Our retrospective study analyzed real-world data of stage 4 sarcoma patients treated with pazopanib in our department in the past 10 years. Data were collected from the Medworks medical system, which is used for daily work in our center. A total of 99 patients were included: 46 men and 53 women The median age at the diagnosis was 49.8 years. The most common histological subtypes were leiomyosarcoma and synovial sarcoma. All patients received 800 mg of pazopanib per day, which was reduced to 400 mg in the event of toxicity. Treatment was continued until disease progression or unmanageable toxicity. The primary endpoint of the study was progression-free survival and the secondary endpoints were overall survival, overall response rate and disease control rate. The results in relation to demographic data, previous treatments, localizations of primary tumors and metastasis and histological subtypes were analyzed. In our center pazopanib was most frequently used in the third line. In total, 61 patients received perioperative therapy; the most common regimen used in the metastatic setting was VIP. Median PFS and OS were 3 months and 7 months, respectively. ORR was 14% and DCR was 40.45%. Dose reductions were necessary during the treatment of 56 patients. Hematological toxicity was detected in 23% of cases, with the most frequent events being grade 1 thrombocytopenia and grade 2 leukocytopenia. Non-hematological adverse events were documented in half of the patients. Pazopanib was more effective in earlier lines of treatment. Compared to the PALETTE phase 3 trial more patients received perioperative therapy, median PFS and OS were shorter (3 months vs. 4.6 months and 7 months vs. 11.9 months) and ORR was higher (14% vs. 9%) in our patient population. Dose reductions were more frequent in our center. Pazopanib is a therapeutic option for the treatment of advanced soft tissue sarcoma, also according to real-world data. Further investigations are needed to select patients who can benefit the most from pazopanib and to determine the most appropriate sequence of therapy.
Insights
This study found pazopanib (a tyrosine-kinase inhibitor) showed moderate effectiveness in advanced soft tissue sarcoma patients. Real-world data indicated shorter progression-free survival and overall survival compared to clinical trials, with frequent dose reductions due to toxicity.
Area of Science:
- Oncology
- Pharmacology
- Medical Data Analysis
Background:
- Pazopanib is a tyrosine-kinase inhibitor used for advanced soft tissue sarcomas.
- Real-world data on pazopanib's effectiveness in stage 4 sarcoma is crucial for clinical practice.
Purpose of the Study:
- To analyze real-world data of advanced soft tissue sarcoma patients treated with pazopanib.
- To evaluate progression-free survival (PFS), overall survival (OS), overall response rate (ORR), and disease control rate (DCR).
- To assess the impact of demographic data, previous treatments, tumor characteristics, and toxicity on pazopanib efficacy.
Main Methods:
- Retrospective analysis of 99 stage 4 soft tissue sarcoma patients treated with pazopanib over 10 years.
- Data collected from the Medworks medical system.
- Pazopanib dosage: 800 mg daily, reduced to 400 mg for toxicity; treatment continued until progression or toxicity.
Main Results:
- Median PFS was 3 months, median OS was 7 months, ORR was 14%, and DCR was 40.45%.
- Pazopanib was most frequently used as a third-line treatment.
- Dose reductions were required in 56 patients; hematological toxicity in 23% and non-hematological in 50%.
Conclusions:
- Pazopanib is a viable treatment option for advanced soft tissue sarcoma based on real-world data.
- Efficacy appears higher in earlier lines of treatment.
- Further research is needed to optimize patient selection and treatment sequencing for pazopanib.
Related Concept Videos
Treatment Resistant Cancers
Treatment Resistent Cancers

