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实体瘤的新兴药物治疗方法。

Emerging drug treatments for solid tumours.

作者信息

Schellens J H, Pronk L C, Verweij J

机构信息

Department of Medical Oncology, Rotterdam Cancer Institute/Daniel den Hoed Kliniek, Rotterdam, The Netherlands.

出版信息

Drugs. 1996 Jan;51(1):45-72. doi: 10.2165/00003495-199651010-00005.

Abstract

A number of novel anticancer agents have emerged during the past few decades, which show high activity in preclinical tumour models and promising activity in early trials in patients with solid tumours. Most of the agents have novel and unique mechanisms of action, and show activity against a variety of malignancies, including tumours which are notoriously resistant to systemic treatment. Recently, our understanding of the molecular basis of cancer has increased considerably. This is reflected in the development of agents that are directed at well defined molecular targets, such as the mitotic tubulin/microtubuli system (taxoids), nuclear enzymes (topoisomerase I inhibitors) and cell signal transduction pathways (protein kinase C inhibitors). In addition, significant advances have been made in our understanding of mechanisms of toxicity, especially of cisplatin. This has resulted in the development of agents modulating cisplatin toxicity, among which amifostine (WR-2721) is one of the most promising. The outlined emerging drug therapies with novel anticancer agents and treatment modalities will, it is hoped, result in increased response rates of advanced tumours, longer disease-free and total survival and better palliative care.

摘要

在过去几十年中出现了许多新型抗癌药物,这些药物在临床前肿瘤模型中显示出高活性,并且在实体瘤患者的早期试验中表现出有前景的活性。大多数药物具有新颖独特的作用机制,对多种恶性肿瘤都有活性,包括那些对全身治疗 notoriously resistant 的肿瘤。最近,我们对癌症分子基础的理解有了显著提高。这体现在针对明确分子靶点的药物开发上,如有丝分裂微管蛋白/微管系统(紫杉类)、核酶(拓扑异构酶 I 抑制剂)和细胞信号转导途径(蛋白激酶 C 抑制剂)。此外,我们对毒性机制,尤其是顺铂毒性机制的理解也取得了重大进展。这导致了调节顺铂毒性药物的开发,其中氨磷汀(WR - 2721)是最有前景的药物之一。希望上述新型抗癌药物和治疗方式的新兴药物疗法能够提高晚期肿瘤的缓解率,延长无病生存期和总生存期,并提供更好的姑息治疗。

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