S oft tissue sarcomas are a heterogeneous group of diseases that account for less than 1% of all malignancies in adults, [1] but with more than 100 subtypes. [2] In 50%-60% of cases, the disease involves the extremities. [3] The incidence of soft tissue sarcoma is approximately 3 in 100000. [4] Approximately half of the patients are over the age of 65 years. [5] While the basic treatment of the disease is surgery, pre-operative and post-operative radiotherapy and che-motherapy are frequently used treatment options. In advanced stages of the disease, multikinase inhibitors, such as pazopanib, have also been introduced into routine practice. The reported mean survival of patients with metastatic disease is approximately 12-18 months. [6] In this study, we evaluated patients who received pazopanib therapy for soft tissue sarcoma at the Istanbul University Oncology Institute between January 2010 and August 2021.Objectives: Soft tissue sarcomas are a heterogeneous group of tumors accounting for less than 1% of adult malignancies. In this study, we examined patients who received pazopanib for soft tissue sarcoma. Factors affecting mortality and overall survival in soft tissue sarcoma patients using pazopanib were investigated. Methods: This study is a retrospective single-center study. Results: Fifty-three patients (median age: 42 years) were included. The median duration of follow-up in our cohort was 34 months. Before pazopanib, 37 patients (69.8%) received first-line, 12 patients (22.6%) received second-line and 4 patients (7.5%) received third-line chemotherapy. The median duration of pazopanib therapy was 7 months (range, 1-82). Median progression-free survival (PFS) and median overall survival was 7 months (range, 1-83) and 12 months (range, 1-83), respectively. Patients who received radiotherapy for curative or palliative purposes had significantly longer PFS (p=0.040). Eight patients required dose reduction due to adverse effects. Grade 4 adverse effects occurred in only 2 patients. After pazopanib, 36 patients (67.9%) did not receive any treatment. On Cox regression analysis, not receiving any treatment after pazopanib was associated with 3.052-fold higher mortality. A 1-unit increase in PFS was associated with 1.15-fold lower risk of mortality.
Conclusion:In this study, pazopanib was found to be an effective and safe drug for advanced soft tissue sarcoma. Patients who received palliative radiotherapy for curative or palliative purposes had significantly longer PFS. Receiving treatment after pazopanib and longer PFS was associated with reduced mortality.