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Pazopanib for metastatic soft-tissue sarcoma: A multicenter retrospective study

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dc.contributor.author Koca, S.
dc.contributor.author Beşiroğlu, M.
dc.contributor.author Özçelik, M.
dc.contributor.author Karaca, M.
dc.contributor.author Bilici, M.
dc.contributor.author Hacıoğlu, B.
dc.contributor.author Doğu, G.G.
dc.contributor.author Kaplan, N.B.
dc.contributor.author Oruç, Z.
dc.contributor.author Aydın, D.
dc.contributor.author Dane, F.
dc.date.accessioned 2022-10-06T12:49:53Z
dc.date.available 2022-10-06T12:49:53Z
dc.date.issued 2021
dc.identifier.issn 10781552 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/71562
dc.description.abstract Purpose: Soft tissue sarcomas are associated with a poor prognosis and low chemotherapeutic efficiency. Pazopanib is an orally available multi-tyrosine kinase inhibitor that was explored in patients with non-adipocytic advanced soft tissue sarcomas. The aim of this retrospective study was to evaluate the real life data of single-agent pazopanib efficacy and safety for soft tissue sarcomas in the Turkish population. Materials and methods: We evaluated a total of 103 patients (41 males, 62 females) who received pazopanib for advanced non-adipocytic soft tissue sarcomas diagnosis in eight centers of Turkey, retrospectively. The pazopanib dose was 800 mg once daily. Progression-free survival, overall survival, and adverse events were analyzed. Results: The median age was 50 years (range, 38–58). Majority of the patients had leimyosarcoma (41%). Median progression-free survival was 4.3 months, and the median overall survival was 10.1 months. The main common toxicities were fatigue, anorexia, weight loss, nausea, hypertension, and grade ≥3 toxicities were fatigue, anorexia, weight loss, and liver disorder. Conclusion: Pazopanib is an efficient and tolerable agent and is well tolerated in good performance status patients with relapsed, advanced non-adipocytic soft tissue sarcomas. © The Author(s) 2020.
dc.source Journal of Oncology Pharmacy Practice
dc.title Pazopanib for metastatic soft-tissue sarcoma: A multicenter retrospective study


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