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Combined chemotherapy with cytotoxic and targeted compounds for the management of human malignant pleural mesothelioma.

机译:结合化学疗法与细胞毒性和靶向化合物治疗人类恶性胸膜间皮瘤。

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摘要

Human malignant pleural mesothelioma (hMPM) is an aggressive asbestos-associated cancer, the incidence of which is increasing and which, despite progress in diagnosis and therapy, continues to have a poor prognosis. Asbestos fibers induce aberrant cell signaling, leading to proto-oncogene activation and chemoresistance. In this review, we discuss the evolution of pharmacological management of hMPM up to the most recent advances. Monotherapy with single cytotoxic drugs achieves modest objective response rates, seldom reaching 30%. However, combination regimens using novel drugs and standard molecules are showing gradually improving responses and clinical benefits. Phase II/III studies have identified pemetrexed, a multitarget folate pathway inhibitor in combination with platinum derivatives, and the cisplatin/gemcitabine association as front-line chemotherapy for hMPM. Detailed knowledge of molecular mechanisms of signal transduction and neoangiogenesis in hMPM should aid in the design and screening of other promising compounds such as more efficacious receptor tyrosine kinase inhibitors.
机译:人恶性胸膜间皮瘤(hMPM)是一种侵略性石棉相关癌,其发病率正在增加,尽管在诊断和治疗方面取得了进展,但其预后仍然很差。石棉纤维诱导异常的细胞信号传导,导致原癌基因活化和化学抗性。在这篇综述中,我们讨论了hMPM药理学管理的最新进展。单一细胞毒性药物的单药疗法可达到中等客观缓解率,很少达到30%。然而,使用新药和标准分子的联合疗法显示出逐渐改善的反应和临床益处。 II / III期研究已经确定了培美曲塞(一种多靶点叶酸途径抑制剂,与铂衍生物联合使用)和顺铂/吉西他滨联合疗法是hMPM的一线化疗药物。 hMPM中信号转导和新血管生成的分子机制的详细知识应有助于设计和筛选其他有希望的化合物,例如更有效的受体酪氨酸激酶抑制剂。

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