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Sorafenib for ovarian cancer

机译:索拉非尼治疗卵巢癌

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Introduction: Sorafenib is an unselective inhibitor of multiple kinases which has demonstrated clinical advantage in renal cancer and hepatocellular carcinoma. It inhibits tumor proliferation by targeting receptor accessory factor (Raf) kinase isoforms, inhibiting receptor tyrosine kinases of a variety of pro-angiogenic factors and of several receptor tyrosine kinases involved in neovascularization and tumor development. Areas covered: This review offers an explanation of the mechanism of action and of the pharmacokinetics of sorafenib, and gives readers a complete overview of Phase I and II studies on the clinical efficacy, tolerability and safety of this agent in the setting of ovarian cancer (OC) treatment. Expert opinion: The available results from the studies which investigated the use of sorafenib for OC treatment demonstrated poor clinical benefit either as single agent or in combination therapy. The most promising results have been achieved combining sorafenib with bevacizumab, although overlapping and cumulative toxicities should be taken in consideration. Research should focus its attention to the development of reliable predictive biomarkers to assess response and direct therapy in order to allow patient selection and improving treatment schedules maximizing the clinical benefit and simultaneously minimizing the toxicity related to the chemotherapy. Further studies are needed to evaluate the role of sorafenib in the primary treatment of OC.
机译:简介:索拉非尼是多种激酶的非选择性抑制剂,已在肾癌和肝细胞癌中显示出临床优势。它通过靶向受体辅助因子(Raf)激酶同工型,抑制多种促血管生成因子的受体酪氨酸激酶以及参与新血管形成和肿瘤发展的几种受体酪氨酸激酶来抑制肿瘤增殖。涵盖的领域:这篇综述提供了索拉非尼的作用机理和药代动力学的解释,并为读者提供了有关该药物在卵巢癌中的临床疗效,耐受性和安全性的I期和II期研究的完整概述( OC)处理。专家意见:研究索拉非尼用于OC治疗的研究可获得的结果表明,无论是单药治疗还是联合治疗,临床疗效均不佳。尽管应考虑重叠和累积毒性,但索拉非尼与贝伐单抗联合使用已获得最有希望的结果。研究应将注意力集中在可靠的预测性生物标记物的开发上,以评估反应和直接治疗,以便允许患者选择和改善治疗方案,从而最大程度地提高临床获益,同时最大程度降低与化学疗法相关的毒性。需要进一步的研究来评估索拉非尼在OC的主要治疗中的作用。

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