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Biological insights into effective and antagonistic combinations of targeted agents with chemotherapy in solid tumors

机译:实体药物有效和拮抗靶向药物联合化疗的生物学见解

摘要

The potential for synergistic interactions between anticancer drugs has been used to justify combinations of agents in clinical trials. However, most combinations of targeted agents and chemotherapies have been tested in the clinic without previous systematic evaluation of their potential benefit. Preclinical studies may help in the identification of synergistic or antagonistic interactions. For antineoplastic therapies, these studies may reveal synergy or antagonism of the drug combinations. Synergy occurs when two agents given together produce higher antitumoral activity than the sum of each individual drug. This represents the ideal setting for the development of combinations of targeted agents and chemotherapies. On the other side, certain drug combinations have shown adverse results, indicative of an antagonistic effect. In this article, we review the preclinical molecular bases that justify approved combinations of targeted agents with chemotherapy including examples of synergistic and antagonistic combinations. We also discuss scenarios for rational associations of targeted agents based on biological data and propose strategies that may improve the success of combinations of anticancer agents.
机译:在临床试验中,抗癌药之间协同相互作用的潜力已被用来证明药物组合的合理性。但是,大多数靶向药物和化学疗法的组合已在临床中进行了测试,而未事先对其潜在益处进行系统的评估。临床前研究可能有助于识别协同或拮抗相互作用。对于抗肿瘤疗法,这些研究可能揭示药物组合的协同作用或拮抗作用。当两种药物一起产生的抗肿瘤活性高于每种药物的总和时,就会产生协同作用。这是开发靶向药物和化学疗法组合的理想环境。另一方面,某些药物组合显示出不良结果,表明具有拮抗作用。在本文中,我们回顾了临床前的分子基础,这些基础证明了靶向药物与化学疗法的批准组合是合理的,包括协同和拮抗组合的例子。我们还将讨论基于生物学数据的靶向药物合理关联的方案,并提出可提高抗癌药物组合成功率的策略。

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