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计算机断层扫描和核扫描在癌症免疫诊断成像中的理论局限性。

Theoretical limitations in the immunodiagnostic imaging of cancer with computed tomography and nuclear scanning.

作者信息

Rockoff S D, Goodenough D J, McIntire K R

出版信息

Cancer Res. 1980 Aug;40(8 Pt 2):3054-8.

PMID:6967351
Abstract

In order to help assess the feasibility of using immunologically tagged agents to render tumors detectable with current computed tomographic and nuclear scanners, mathematical formulations were developed to determine the theoretical limits of tumor detection relative to size and depth of the lesions. The results of our analysis suggest that visualization with computed tomography of a tiny tumor (1 sq mm, cross-sectional area) would require binding in the order of 2 x 10(5) iodine atoms/antigenic site, while imaging of a very large (900-sq mm) tumor would require approximately 10(4) atoms/site. Very low energy scanners might reduce these discouraging estimates by an order of 10(2). The immunological imaging of tumors with nuclear scanning appears quite feasible from our formulations, as has been demonstrated by others clinically. Small (1-sq cm) and deep (greater than or equal to 5-cm) tumors appear detectable with uptake ratios of the order of 5 or higher, which seem to be attainable currently. Smaller and deeper tumors require much higher uptake ratios to be detected.

摘要

为了帮助评估使用免疫标记剂使肿瘤能被当前的计算机断层扫描和核扫描仪检测到的可行性,我们开发了数学公式来确定相对于病变大小和深度的肿瘤检测理论极限。我们的分析结果表明,用计算机断层扫描可视化一个微小肿瘤(横截面积1平方毫米)需要每个抗原位点结合约2×10⁵个碘原子,而对一个非常大的(900平方毫米)肿瘤进行成像则需要每个位点约10⁴个原子。极低能量扫描仪可能会使这些令人沮丧的估计降低10²倍。从我们的公式来看,用核扫描对肿瘤进行免疫成像似乎相当可行,正如其他人临床所证明的那样。较小(1平方厘米)且较深(大于或等于5厘米)的肿瘤似乎可以通过约5或更高的摄取率被检测到,目前这似乎是可以实现的。更小且更深的肿瘤需要更高的摄取率才能被检测到。

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