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Effect of Breast Compression on Lesion Characteristic Visibility with Diffraction-Enhanced Imaging

Rationale and Objectives

Conventional mammography can not distinguish between transmitted, scattered, or refracted x-rays, thus requiring breast compression to decrease tissue depth and separate overlapping structures. Diffraction-enhanced imaging (DEI) uses monochromatic x-rays and perfect crystal diffraction to generate images with contrast based on absorption, refraction, or scatter. Because DEI possesses inherently superior contrast mechanisms, the current study assesses the effect of breast compression on lesion characteristic visibility with DEI imaging of breast specimens.

Materials and Methods

Eleven breast tissue specimens, containing a total of 21 regions of interest, were imaged by DEI uncompressed, half-compressed, or fully compressed. A fully compressed DEI image was displayed on a soft-copy mammography review workstation, next to a DEI image acquired with reduced compression, maintaining all other imaging parameters. Five breast imaging radiologists scored image quality metrics considering known lesion pathology, ranking their findings on a 7-point Likert scale.

Results

When fully compressed DEI images were compared to those acquired with approximately a 25% difference in tissue thickness, there was no difference in scoring of lesion feature visibility. For fully compressed DEI images compared to those acquired with approximately a 50% difference in tissue thickness, across the five readers, there was a difference in scoring of lesion feature visibility. The scores for this difference in tissue thickness were significantly different at one rocking curve position and for benign lesion characterizations. These results should be verified in a larger study because when evaluating the radiologist scores overall, we detected a significant difference between the scores reported by the five radiologists.

Conclusions

Reducing the need for breast compression might increase patient comfort during mammography. Our results suggest that DEI may allow a reduction in compression without substantially compromising clinical image quality.

Breast cancer imparts distinct and measurable changes in breast tissue at the cellular level. Conventional mammography attempts to detect these changes by using absorption contrast based on the spatial distribution of x-ray attenuation. This contrast mechanism requires compression of the breast between radiolucent plates to decrease x-ray path length and separate overlapping breast structures, while creating more uniform thickness for even exposure levels throughout the breast. This technique effectively reduces scatter, decreases subject radiation dose and dramatically improves image quality. The American College of Radiology suggests a maximum compression force for mammography between 25 and 40 pounds . Many women report pain associated with breast compression, potentially contributing to noncompliance with annual screening mammography recommendations for women in the United States older than age 40 .

A recent study that used Monte Carlo simulations suggested that the typical level of breast compression for digital mammography (DM) could be decreased by approximately 10% with minimal impact on image quality . However, even with maximal breast compression, absorption contrast does not always provide sufficient contrast because of minimal differences in physical and electron density between normal and cancerous tissues. The microscopic and macroscopic alterations induced by cancer in breast tissue may cause x-ray refraction, minute changes in the direction of x-ray propagation. Phase contrast imaging techniques that acquire images based on x-ray refraction contrast may have applications in breast imaging .

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Materials and methods

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Specimen Selection

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DEI

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Figure 1, Diffraction-enhanced imaging (DEI) system setup. An intense, collimated polychromatic synchrotron x-ray beam is made monochromatic by a series of two perfect silicon crystals referred to as the monochromator. The monochromatic beam interacts with the object before becoming incident upon the third perfect crystal, referred to as the analyzer crystal. The analyzer crystal diffracts the x-ray based on its rocking curve, only reflecting x-rays that fall within a narrow acceptance window. Manipulating the angle of the analyzer crystal allows the selection of image contrast based on either absorption or refraction.

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Figure 2, The diffraction-enhanced imaging (DEI) rocking curve. Reflectivity is equal to the intensity at the detector (I) divided by the intensity delivered to the object (I 0 ). When positioned at the ±½ W D , 50% of incident x-rays are diffracted onto the detector. Refraction above or below the plane of the incident x-ray beam will cause an increase or decrease in x-ray intensity at the detector. Maximal reflectivity occurs and excellent scatter rejection occurs at the peak rocking curve positions, and refraction of x-rays will decrease intensity regardless of the direction of refraction.

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Full-field Digital Mammography

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Specimen Assessment

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Reader Study

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Statistical Methods

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Results

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Table 1

Measured Specimen Thicknesses and Percent Densities

Glandular (%) Adipose (%) Uncompressed Thickness (cm) Half- compressed Thickness (cm) Fully Compressed Thickness (cm) Specimen 1 10 90 3.9 2.9 2.0 Specimen 2 20 80 3.9 2.9 2.0 Specimen 3 30 70 3.9 2.9 2.0 Specimen 4 40 60 3.9 2.9 2.0 Specimen 5 90 10 6.7 6.1 3.4 Specimen 6 30 70 5.8 4.3 2.9 Specimen 7 50 50 5.1 3.8 2.5 Specimen 8 10 90 7.1 5.3 3.6 Specimen 9 40 60 6.5 4.9 4.0 Specimen 10 20 80 6.0 4.7 3.2 Specimen 11 30 70 8.0 6.7 5.5

Specimens were compressed an average of 24.7 ± 1.2 (%) of resting thickness at half-compression and 46.6 ± 4.6 (%) of resting thickness at full compression. The glandular/fatty composition of each specimen was assessed by an experienced radiologist.

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Figure 3, Effect of tissue thickness on cancerous lesion visibility. The circled region of interest contained extensive comedo-type ductal carcinoma in situ of nuclear grade 3 with necrosis and lobule cancerization, without calcifications. The left panel depicts a digital mammogram of a mastectomy specimen. The panel on the right shows the same lesion, cropped, shown fully, half-, and uncompressed at each diffraction-enhanced imaging (DEI) rocking curve position.

Figure 4, Effect of tissue thickness on benign lesion visibility. All images were acquired at 30 keV. This region of in terest (ROI) represents a vascular calcification. Digital mammography (DM) images are displayed in the first column (a, b) . The second column (c, d) represents images acquired at the peak of the rocking curve, and the third column (e, f) were acquired at the + ½W D . The fully compressed DM image (a) was acquired with a surface dose of 7.46 mGy, whereas the dose required to acquire an optimal image of the uncompressed specimen (b) was 30.93 mGy. Diffraction-enhanced imaging (DEI) images were acquired with relatively constant doses at all thicknesses, with an average dose of 0.30 mGy for these images.

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Figure 5, Trend in lesion perception as tissue thickness increases. The average scores reported by the radiologists were plotted as a function of the difference in tissue thickness, measured in cm. The score values could range from −3 (the fully compressed diffraction-enhanced imaging [DEI] image displays lesion feature visibility supportive of the diagnosis significantly worse than the DEI image acquired with reduced compression), to 0 (no difference between either image), to +3 (the fully compressed DEI image displays lesion feature visibility supportive of the diagnosis significantly better than the DEI image acquired with reduced compression). Linear trendlines, calculated individually for DEI absorption and DEI refraction, are shows as solid lines. Although the scores could have ranged from −3 to +3, when the scores were averaged for DEI refraction images and DEI absorption images for a specific difference in tissue thickness, these scores did not occupy the entire possible range. Moreover, the standard deviation led to some error bars that rose above the +3 maximum possible score.

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Table 2

Reader Study Results: Effect of Specimen Type

Difference in Tissue Thickness Mean Standard Error 95% CI_P_ Value Cadaveric 25% 0.3863 0.3357 (−0.273, 1.046) .2504 50% 0.9678 0.3357 (0.308, 1.627).0041 Mastectomy 25% 0.1019 0.2331 (−0.356, 0.560) .6623 50% 0.2212 0.2331 (−0.237, 0.679) .3430

The P values were calculated based on the calculated means, standard errors, and a 95% confidence interval (CI). Radiologist perception of lesion visibility for a 50% difference in tissue thickness in cadaveric specimens approached significance (bold).

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Table 3

Reader Study Results: Effect of Rocking Curve Position

Difference in Tissue Thickness Mean Standard Error 95% CI_P_ Value −½W D 25% 0.2631 0.2002 (−0.130, 0.656) .1892 50% 0.7818 0.2002 (0.389, 1.175).0001 Peak 25% 0.1679 0.2002 (−0.225, 0.561) .4020 50% 0.5056 0.2002 (0.113, 0.899).0118 +½W D 25% 0.3012 0.2002 (−0.092, 0.694) .1329 50% 0.4961 0.2002 (0.103, 0.889).0135

The P values were calculated based on the calculated means, standard errors, and a 95% confidence interval (CI). For a 50% difference in tissue thickness, radiologist perception of lesion visibility was different for each rocking curve position, but we only found statistical significance at the −½ W D position (bold). The reported means and standard error values are estimates from the mixed effect model.

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Table 4

Reader Study Results: Effect of Lesion Type

Difference in Tissue Thickness Mean Standard Error 95% CI_P_ Value Atypical 25% 0.3052 0.4643 (−0.607, 1.217) .5113 50% 0.5500 0.4643 (−0.362, 1.462) .2367 Benign 25% 0.3719 0.1454 (0.086, 0.657).0108 50% 0.6389 0.1454 (0.353, 0.925)<.0001 In situ 25% 0.3941 0.2932 (−0.182, 0.970) .1794 50% 0.7723 0.2932 (0.196, 1.348).0087 Malignant 25% −0.09481 0.2641 (−0.614, 0.424) .71975 50% 0.4167 0.2651 (−0.102, 0.935) .1152

The P values were calculated based on the calculated means, standard errors, and a 95% confidence interval (CI). Difference in the perception of benign lesion visibility approached significance for a 25% difference in tissue thickness, and achieved significance at a 50% difference in tissue thickness (bold). In situ lesion visibility also approached significance for a 50% difference in tissue thickness.

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Discussion

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Acknowledgments

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