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嘌呤类似物的观点。

Perspectives on purine analogues.

作者信息

Cheson B D

机构信息

Cancer Therapy Evaluation Program, National Cancer Institute, Bethesda, Maryland, USA.

出版信息

Hematol Cell Ther. 1996 Dec;38 Suppl 2:S109-16.

PMID:9137964
Abstract

The purine analogs, fludarabine, 2-chlorodeoxy-adenosine, and 2'-deoxycoformycin, have revolutionized our approach to the treatment of a variety of indolent lymphoid malignancies. Because of their impressive single agent activity, they should be considered as an initial therapeutic option, not only for hairy cell leukemia, but also for chronic lymphocytic leukemia, indolent non-Hodgkin's lymphomas, and Waldenström's macroglobulenemia. Combinations of purine analogs with alkylatng agents, topisomerase II inhibitors, and other new compounds are in development, and their role as radiation sensitizers is being explored in clinical trials. Substantial activity has also been noted in several of the rheumatologic and immunologic disorders, and in multiple sclerosis. Continued progress requires innovative strategies which can modulate the biology and immunology of these diseases toward the goal of curing these patients.

摘要

嘌呤类似物,氟达拉滨、2-氯脱氧腺苷和2'-脱氧助间型霉素,彻底改变了我们治疗多种惰性淋巴系统恶性肿瘤的方法。由于它们令人印象深刻的单药活性,不仅对于毛细胞白血病,而且对于慢性淋巴细胞白血病、惰性非霍奇金淋巴瘤和华氏巨球蛋白血症,都应将它们视为初始治疗选择。嘌呤类似物与烷化剂、拓扑异构酶II抑制剂及其他新化合物的联合应用正在研发中,并且它们作为辐射增敏剂的作用正在临床试验中进行探索。在几种风湿性和免疫性疾病以及多发性硬化症中也已注意到显著活性。持续的进展需要创新策略,这些策略能够调节这些疾病的生物学和免疫学,以实现治愈这些患者的目标。

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