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Clinical Benefit of Pazopanib in a Patient with Metastatic Chondrosarcoma: A Case Report and Review of the Literature

机译:帕唑帕尼治疗转移性软骨肉瘤的临床疗效:一例报告并文献复习

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摘要

Chondrosarcoma is a rare malignancy characterized by the production of cartilage matrix, displaying heterogeneous histopathology and clinical behavior. Due to lack of effective treatment for advanced disease, the clinical management of metastatic chondrosarcoma is exceptionally challenging. Chondrosarcomas harbor molecular abnormalities, such as overexpression of platelet-derived growth factor receptor (PDGFR)-alpha and PDGFR-beta, which are required for cancer development, progression, and metastasis. Pazopanib is a potent and selective multitargeted tyrosine kinase inhibitor, which co-inhibits stem cell growth factor receptor (c-KIT), fibroblast growth factor receptor (FGFR), PDGFR, and vascular endothelial growth factor receptor (VEGFR) and has demonstrated clinical activity in patients with advanced previously treated soft tissue sarcoma. Herein, we describe the unique case of a patient with metastatic chondrosarcoma who derived clinical benefit from pazopanib after first-line chemotherapy failure.
机译:软骨肉瘤是一种罕见的恶性肿瘤,其特征在于软骨基质的产生,表现出异质的组织病理学和临床行为。由于缺乏对晚期疾病的有效治疗,转移性软骨肉瘤的临床管理极具挑战性。软骨肉瘤具有分子异常,例如血小板衍生的生长因子受体(PDGFR)-α和PDGFR-β的过度表达,这是癌症发展,进展和转移所必需的。 Pazopanib是一种有效且选择性的多靶点酪氨酸激酶抑制剂,可共同抑制干细胞生长因子受体(c-KIT),成纤维细胞生长因子受体(FGFR),PDGFR和血管内皮生长因子受体(VEGFR),并已证明其临床活性先前已接受治疗的晚期软组织肉瘤患者。在此,我们描述了一线化疗失败后从帕唑帕尼获得临床益处的转移性软骨肉瘤患者的独特病例。

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