通过计算机辅助定量图像分析来测量来自癌前病变(上皮内瘤变)的癌症化学预防试验的终点标志物。

C. Boone, G. Kelloff
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引用次数: 1

摘要

癌症化学预防临床试验的终点标记是由上皮内瘤变本身的癌前病变的形态学特征发展而来的,通过计算机辅助定量图像分析来测量。标记物包括增殖分数增加(mb -1阳性核面积百分比);核DNA含量(DNA倍性),包括DNA含量超过单倍体数量的5倍(5c超成率);核和核仁的形态测量学;以及核染色质模式的紊乱,以马尔可夫参数和其他功能为特征。图像分析的一个重要的新进展是“平铺”过程,在该过程中,在x40放大率下,给定组织学切片的数百个完整监控图像场的大小被缩小并无缝融合,以产生x1.25放大率下的组织学切片的单个图像。操作员可以查看低功率图像,并通过鼠标点/点击检索x40放大的任何所需区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endpoint markers for cancer chemoprevention trials derived from the lesion of precancer (intraepithelial neoplasia) measured by computer-assisted quantitative image analysis.
Endpoint markers for cancer chemoprevention clinical trials are described that are developed from the morphological properties of the precancerous lesion of intraepithelial neoplasia itself, as measured by computer-assisted quantitative image analysis. The markers include increased proliferative fraction (percentage MIB-1 positive nuclear area); nuclear DNA content (DNA ploidy), including DNA content exceeding fivefold the haploid amount (5C-exceeding rate); nuclear/nucleolar morphometry; and disorganization of nuclear chromatin pattern as characterized by Markovian parameters and other functions. A significant new advance in image analysis is the process of "tiling," in which hundreds of full monitor image fields of a given histological section at x40 magnification are reduced in size and fused seamlessly to produce a single image of the histological section at x1.25 magnification. The operator may review the low-power image and retrieve x40 magnification of any desired area by point/clicking with a mouse.
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