Current results of the screening program at the division of cancer treatment, national cancer institute

Abraham Goldin , John M. Venditti , John S. Macdonald , Franco M. Muggia , Jane E. Henney , Vincent T. Devita Jr.
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引用次数: 217

Abstract

The prospective screening program at the Division of Cancer Treatment, National Cancer Institute, has now been in operation for several years and is making steady progress in the identification of new synthetic compounds and natural products of potential interest for the clinic. Data are presented on four categories of drugs that have been tested in the new screening panel: (a) clinically established antitumor agents; (b) new drugs and drugs for which there is renewed clinical interest based on activity in the new screen and previously inadequate clinical trial; (c) drugs in the initial phases of clinical trial; (d) compounds in development. An analysis of the data is presented, taking into account a series of important questions that are being addressed prospectively to the new screen. Although the ability to provide definitive answers must await feedback from clinical testing of compounds recommended by the screen, some generalizations appear to be emerging, and these are discussed. A comparison is made of the activity of drugs in the treatment of human tumors growing in two sites, subcutaneously and under the renal capsule. The subrenal capsule model appears to be somewhat more sensitive to drugs than the subcutaneous model and may provide certain advantages for initial panel testing. Attention is drawn to the potential usefulness in a screening program of the newly developed clonogenic techniques for growing human tumors. The screening program at the Division of Cancer Treatment is viewed as a dynamic entity, subject to modification in accordance with acquired experience.

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国家癌症研究所癌症治疗部的筛查项目的最新结果
美国国家癌症研究所癌症治疗部的前瞻性筛查项目已经运行了几年,在鉴定新的合成化合物和临床潜在兴趣的天然产物方面取得了稳步进展。数据介绍了在新的筛选小组中测试的四类药物:(a)临床建立的抗肿瘤药物;(b)新药和基于新筛选活动和先前不充分的临床试验而重新引起临床兴趣的药物;(c)处于临床试验初期的药物;(d)正在开发的化合物。提出了对数据的分析,考虑到新屏幕正在解决的一系列重要问题。虽然提供明确答案的能力必须等待筛选推荐的化合物的临床试验反馈,但一些概括似乎正在出现,并对其进行讨论。比较了药物治疗生长在皮下和肾包膜下两个部位的人类肿瘤的活性。与皮下模型相比,肾下胶囊模型似乎对药物更敏感,可能为初始面板试验提供某些优势。注意到潜在的有用性,在筛选程序的新开发的克隆技术生长的人类肿瘤。癌症治疗部门的筛查项目被视为一个动态的实体,可以根据获得的经验进行修改。
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