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全数字化乳腺摄影与乳腺密度:校准与未校准测量值的比较。

Full field digital mammography and breast density: comparison of calibrated and noncalibrated measurements.

机构信息

Cancer Prevention & Control Division, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.

出版信息

Acad Radiol. 2011 Nov;18(11):1430-6. doi: 10.1016/j.acra.2011.07.011.

DOI:10.1016/j.acra.2011.07.011
PMID:21971260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3190123/
Abstract

RATIONALE AND OBJECTIVES

Mammographic breast density is an important and widely accepted risk factor for breast cancer. A statement about breast density in the mammographic report is becoming a requirement in many States. However, there is significant inter-observer variation between radiologists in their interpretation of breast density. A properly designed automated system could provide benefits in maintaining consistency and reproducibility. We have developed a new automated and calibrated measure of breast density using full field digital mammography (FFDM). This new measure assesses spatial variation within a mammogram and produced significant associations with breast cancer in a small study. The costs of this automation are delays from advanced image and data analyses before the study can be processed. We evaluated this new calibrated variation measure using a larger dataset than previously. We also explored the possibility of developing an automated measure from unprocessed (raw data) mammograms as an approximation for this calibrated breast density measure.

MATERIALS AND METHODS

A case-control study comprised of 160 cases and 160 controls matched by age, screening history, and hormone replacement therapy was used to compare the calibrated variation measure of breast density with three variants of a noncalibrated measure of spatial variation. The operator-assisted percentage of breast density measure (PD) was used as a standard reference for comparison. Odds ratio (OR) quartile analysis was used to compare these measures. Linear regression analysis was applied to assess the calibration's impact on the raw pixel distribution.

RESULTS

All breast density measures showed significant breast cancer associations. The calibrated spatial variation measure produced the strongest associations (OR: 1.0 [ref.], 4.6, 4.3, 7.4). The associations for PD were diminished in comparison (OR: 1.0 [ref.], 2.7, 2.9, 5.2). Two additional non-calibrated measures restricted in region size also showed significant associations (OR: 1.0 [ref.], 2.9, 4.4, 5.4), and (OR: 1.0 [ref.], 3.5, 3.1, 4.9). Regression analyses indicated the raw image mean is influenced by the calibration more so than its standard deviation.

CONCLUSION

Breast density measures can be automated. The associated calibration produced risk information not retrievable from the raw data representation. Although the calibrated measure produced the stronger association, the non-calibrated measures may offer an alternative to PD and other operator based methods after further evaluation, because they can be implemented automatically with a simple processing algorithm.

摘要

原理和目的

乳腺密度是乳腺癌的一个重要且被广泛认可的风险因素。在许多州,在乳腺 X 光报告中对乳腺密度进行说明已经成为一项要求。然而,放射科医生在解释乳腺密度方面存在显著的观察者间差异。一个设计合理的自动化系统可以在保持一致性和可重复性方面提供好处。我们使用全视野数字化乳腺 X 线摄影(FFDM)开发了一种新的自动和校准的乳腺密度测量方法。这项新的测量方法评估了乳腺 X 光片中的空间变化,并在一项小型研究中与乳腺癌显著相关。这种自动化的成本是在研究可以处理之前,从先进的图像和数据分析中产生的延迟。我们使用比以前更大的数据集来评估这个新的校准变异测量。我们还探索了从未经处理的(原始数据)乳腺 X 光片中开发自动测量方法的可能性,作为这种校准乳腺密度测量的近似值。

材料和方法

采用病例对照研究,纳入了 160 例病例和 160 例年龄、筛查史和激素替代疗法匹配的对照,比较了乳腺密度的校准变异测量与三种非校准空间变异测量的差异。操作员辅助的乳腺密度百分比(PD)测量被用作比较的标准参考。比值比(OR)四分位分析用于比较这些措施。线性回归分析用于评估校准对原始像素分布的影响。

结果

所有的乳腺密度测量都与乳腺癌有显著关联。校准后的空间变异测量产生了最强的关联(OR:1.0[参考],4.6、4.3、7.4)。与 PD 相比,PD 的相关性减弱(OR:1.0[参考],2.7、2.9、5.2)。另外两个区域大小受限的非校准测量也显示出显著的相关性(OR:1.0[参考],2.9、4.4、5.4)和(OR:1.0[参考],3.5、3.1、4.9)。回归分析表明,原始图像的平均值比其标准差更容易受到校准的影响。

结论

乳腺密度测量可以实现自动化。相关的校准提供了从原始数据表示中无法获取的风险信息。虽然校准后的测量方法产生了更强的关联,但非校准测量方法可能在进一步评估后成为 PD 和其他基于操作者的方法的替代方法,因为它们可以通过简单的处理算法自动实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/ed5b5f32cf9c/nihms315292f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/c5449f8c99cc/nihms315292f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/bc25ae2c1051/nihms315292f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/57d61a5ddf05/nihms315292f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/ed5b5f32cf9c/nihms315292f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/c5449f8c99cc/nihms315292f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/bc25ae2c1051/nihms315292f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/57d61a5ddf05/nihms315292f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e073/3190123/ed5b5f32cf9c/nihms315292f4.jpg

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