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Targeted treatment for advanced soft tissue sarcoma: profile of pazopanib

机译:晚期软组织肉瘤的靶向治疗:帕唑帕尼的概况

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摘要

Soft tissue sarcomas comprise approximately 1% of all adult solid malignancies. While chemotherapy is the mainstay of treatment for patients with metastatic or inoperable disease, overall survival for these patients is approximately 12 months, highlighting the need for novel agents. Both laboratory and clinical data have suggested that antiangiogenic agents may have a role in the treatment of soft tissue sarcomas. Pazopanib is a multitargeted receptor tyrosine kinase inhibitor with antiangiogenic activity. The randomized, double-blind, placebo-controlled, Phase III PALETTE (pazopanib for metastatic soft-tissue sarcoma) study demonstrated improved progression-free survival in patients receiving pazopanib compared with placebo. In this review, we discuss the rationale and clinical evidence for the use of pazopanib in the treatment of metastatic and inoperable soft tissue sarcomas.
机译:软组织肉瘤约占所有成人实体恶性肿瘤的1%。尽管化学疗法是转移性或不可手术性疾病患者的主要治疗手段,但这些患者的总生存期约为12个月,这凸显了对新型药物的需求。实验室和临床数据均表明,抗血管生成剂可能在软组织肉瘤的治疗中起作用。帕唑帕尼是一种具有抗血管生成活性的多靶点受体酪氨酸激酶抑制剂。随机,双盲,安慰剂对照的III期PALETTE(帕唑帕尼用于转移性软组织肉瘤)研究表明,与安慰剂相比,接受帕唑帕尼的患者无进展生存期有所改善。在这篇综述中,我们讨论了使用帕唑帕尼治疗转移性和无法手术的软组织肉瘤的理由和临床证据。

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