Feigl P, Breslow N E, Laszlo J, Priore R L, Taylor W F
J Natl Cancer Inst. 1981 Nov;67(5):1017-24.
The evolution of the Centralized Cancer Patient Data System, a cooperative venture of the 21 comprehensive cancer centers in the United States, and its structure at the end of 3 years of data collection are described. Functions of the data system are detailed in terms of input and output. It is concluded that the short-run objective of establishing a data system to provide high-quality patient data that ae 21 comprehensive cancer centers in the United States, and its structure at the end of 3 years of data collection are described. Functions of the data system are detailed in terms of input and output. It is concluded that the short-run objective of establishing a data system to provide high-quality patient data that ae 21 comprehensive cancer centers in the United States, and its structure at the end of 3 years of data collection are described. Functions of the data system are detailed in terms of input and output. It is concluded that the short-run objective of establishing a data system to provide high-quality patient data that are comparable among cancer centers has been largely accomplished. Moreover, the very process of setting up the national data system has benefited the participating centers by upgrading their individual cancer registries. For the future, the goal is to realize the research potential of this new cooperative data collection mechanism, as well as the accumulating data themselves. Progress toward the long-term goal is just beginning.
本文描述了美国21家综合癌症中心合作建立的集中式癌症患者数据系统的发展历程及其在3年数据收集期末的结构。从输入和输出方面详细阐述了该数据系统的功能。结论是,建立一个能提供高质量患者数据且各癌症中心数据具有可比性的数据系统这一短期目标已基本实现。此外,建立国家数据系统的过程本身也使参与的中心受益,提升了它们各自的癌症登记系统。展望未来,目标是挖掘这种新的合作数据收集机制以及积累的数据本身的研究潜力。朝着长期目标前进的征程才刚刚开始。