癌症化学预防的最新进展。

IF 3.5 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Cancer cells (Cold Spring Harbor, N.Y. : 1989) Pub Date : 1991-02-01
S M Lippman, W N Hittelman, R Lotan, U Pastorino, W K Hong
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引用次数: 0

摘要

ccpc90会议和研讨会包括基础科学家的报告,描述了用于研究上皮癌变及其相关生化和分子改变的关键体外和体内模型系统。会议的一个主要主题是识别特定致癌阶段的标志物。目前的工作主要集中在定义瘤前病变的生物学,多步骤癌变过程中的关键特定分子事件,以及人类癌变过程中病毒、行为、饮食和遗传因素之间的动态相互作用。分子流行病学和遗传易感性的研究正在确定新的危险群体,并有助于制定预防战略。会议的另一个主要主题是现场致癌作用的概念,以及对致癌物质暴露组织的“风险”研究。几位研究人员讨论的一个具体例子是头颈部和肺癌中SPT的发展问题。描述了用于早期检测和作为中间终点的生物标志物的新研究。后一种应用,如果在人体试验中得到验证,可能允许化学预防剂的短期筛选和确定III期化学预防试验的最佳剂量/时间表。这些生物标志物试验可以作为临床前工作和全面随机试验之间的桥梁。介绍了主要III期临床试验的现状。化学预防试验的主要问题包括(1)药物、剂量和时间表的选择;(2)缺乏药理学和药物质量控制;(5)依从性(退出和加入);(6)特定试验的可行性/招募问题。
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Recent advances in cancer chemoprevention.

The CCPC 90 conference and workshop included presentations by basic scientists describing the key in vitro and in vivo model systems used to study epithelial carcinogenesis and its associated biochemical and molecular alterations. A major conference theme was the identification of markers identifying specific carcinogenic stages. Current work focuses on defining the biology of preneoplasia, the critical specific molecular events in multistep carcinogenesis, and the dynamic interplay between viral, behavioral, dietary, and genetic factors in human carcinogenesis. Studies of molecular epidemiology and genetic susceptibility are identifying new risk groups and contributing to preventive strategies. Another major theme of the conference was the concept of field carcinogenesis and the study of carcinogen-exposed tissue "at risk" for the development of cancer. A specific example discussed by several investigators was the issue of SPT development in head and neck and lung cancers. Novel studies of biologic markers for use in early detection and as intermediate end points were described. The latter application, if validated in human trials, may allow short-term screening of chemopreventive agents and determinations of optimal doses/schedules for phase III chemoprevention trials. These biomarker trials may serve as a bridge between preclinical work and full-scale randomized trials. The status of the major phase III clinical trials was presented. Major problems in chemoprevention trials include (1) selection of agents, doses, and schedules, (2) lack of pharmacologic and pharma quality control, (5) adherence (drop-out and drop-in), and (6) trial-specific feasibility/recruitment, issues.

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