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Annual breast magnetic resonance imaging (MRI) plus mammography is the standard of care for screening women with inherited BRCA1/2 mutations. However, long-term breast cancer-related mortality with screening is unknown. Between 1997 and June 2011, 489 previously unaffected BRCA1/2 mutation carriers aged 25 to 65 years were screened with annual MRI plus mammography on our study. Thereafter, participants were eligible to continue MRI screening through the high-risk Ontario Breast Screening Program. In 2019, our data were linked to the Ontario Cancer Registry of Cancer Care Ontario to identify all incident cancers, vital status and causes of death. Observed breast cancer mortality was compared to expected mortality for age-matched women in the general population. There were 91 women diagnosed with breast cancer (72 invasive and 19 ductal carcinoma in situ (DCIS)) with median follow-up 7.4 (range: 0.1 to 19.2) years. Four deaths from breast cancer were observed, compared to 2.0 deaths expected (standardized mortality ratio (SMR) 2.0, p = 0.14). For the 489 women in the study, the probability of not dying of breast cancer at 20 years from the date of the first MRI was 98.2%. Annual screening with MRI plus mammography is a reasonable option for women who decline or defer risk-reducing mastectomy.

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Breast MRI is frequently performed prior to breast conserving surgery in order to assess the location and extent of the lesion. Ideally, the surgeon should also be able to use the image information during surgery to guide the excision and this requires that the MR image is co-registered to conform to the patient's position on the operating table. Recent progress in MR imaging techniques has made it possible to obtain high quality images of the patient in the supine position which significantly reduces the complexity of the registration task. Surface markers placed on the breast during imaging can be located during surgery using an external tracking device and this information can be used to co-register the images to the patient. There remains the problem that in most clinical MR scanners the arm of the patient has to be placed parallel to the body whereas the arm is placed perpendicular to the patient during surgery. The aim of this study is to determine the accuracy of co-registration based on a surface marker approach and, in particular, to determine what effect the difference in a patient's arm position makes on the accuracy of tumour localization. Obtaining a second MRI of the patient where the patient's arm is perpendicular to body axes (operating room position) is not possible. Instead we obtain a secondary MRI scan where the patient's arm is above the patient's head to validate the registration. Five patients with enhancing lesions ranging from 1.5 to 80 cm(3) in size were imaged using contrast enhanced MRI with their arms in two positions. A thin-plate spline registration scheme was used to match these two configurations. The registration algorithm uses the surface markers only and does not employ the image intensities. Tumour outlines were segmented and centre of mass (COM) displacement and Dice measures of lesion overlap were calculated. The relationship between the number of markers used and the COM-displacement was also studied. The lesion COM-displacements ranged from 0.9 to 9.3 mm and the Dice overlap score ranged from 20% to 80%. The registration procedure took less than 1 min to run on a standard PC. Alignment of pre-surgical supine MR images to the patient using surface markers on the breast for co-registration therefore appears to be feasible.

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This article is based on an introductory lecture given for the past many years during the "MR Physics and Techniques for Clinicians" course at the Annual Meeting of the ISMRM. This introduction is not intended to be a comprehensive overview of the field, as the subject of magnetic resonance imaging (MRI) physics is large and complex. Rather, it is intended to lay a conceptual foundation by which magnetic resonance image formation can be understood from an intuitive perspective. The presentation is nonmathematical, relying on simple models that take the reader progressively from the basic spin physics of nuclei, through descriptions of how the magnetic resonance signal is generated and detected in an MRI scanner, the foundations of nuclear magnetic resonance (NMR) relaxation, and a discussion of the Fourier transform and its relation to MR image formation. The article continues with a discussion of how magnetic field gradients are used to facilitate spatial encoding and concludes with a development of basic pulse sequences and the factors defining image contrast.

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Fast imaging applications in magnetic resonance imaging (MRI) frequently involve undersampling of k-space data to achieve the desired temporal resolution. However, high temporal resolution images generated from undersampled data suffer from aliasing artifacts. In radial k-space sampling, this manifests as undesirable streaks that obscure image detail. Compressed sensing reconstruction has been shown to reduce such streak artifacts, based on the assumption of image sparsity. Here, compressed sensing is implemented with three different radial sampling schemes (golden-angle, bit-reversed, and random sampling), which are compared over a range of spatiotemporal resolutions. The sampling methods are implemented in static scenarios where different undersampling patterns could be compared. Results from point spread function studies, simulations, phantom and in vivo experiments show that the choice of radial sampling pattern influences the quality of the final image reconstructed by the compressed sensing algorithm. While evenly undersampled radial trajectories are best for specific temporal resolutions, golden-angle radial sampling results in the least overall error when various temporal resolutions are considered. Reduced temporal fluctuations from aliasing artifacts in golden-angle sampling translates to improved compressed sensing reconstructions overall.

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PURPOSE: To achieve high-quality unilateral supine breast magnetic resonance imaging (MRI) as a step to facilitate image aiding of clinical applications, which are often performed in the supine position. Contrast-enhanced breast MRI is a powerful tool for the diagnosis of cancer. However, prone patient positioning typically used for breast MRI hinders its use for image aiding. MATERIALS AND METHODS: A fixture and a flexible four-element receive coil were designed for patient-specific shaping and placement of the coil in close conformity to the supine breast. A 3D spoiled gradient sequence was modified to incorporate compensation of respiratory motion. The entire setup was tested in volunteer experiments and in a pilot patient study. RESULTS: The flexible coil design and the motion compensation produced supine breast MR images of high diagnostic value. Variations in breast shape and in tissue morphology within the breast were observed between a supine and a diagnostic prone MRI of a patient. CONCLUSION: The presented supine breast MRI achieved an image quality comparable to diagnostic breast MRI. Since supine positioning is common in many clinical applications such as ultrasound-guided breast biopsy or breast-conserving surgery, the registration of the supine images will aid these applications.

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Although magnetic resonance imaging (MRI) is much more sensitive than mammography for detecting early invasive breast cancer, in many high-risk screening studies MRI was less sensitive than mammography for detecting ductal carcinoma in situ (DCIS). We reviewed our experience detecting DCIS in our single center study of annual MRI, mammography, ultrasound and clinical breast examination (CBE) for screening very high-risk women. All cases of DCIS±microinvasion and invasive cancer were compared in two time frames: before (period A) and after (period B) July 2001-when we acquired expertise in the detection of DCIS with MRI-with respect to patient demographics, method of detection, and rates of detection of invasive cancer and DCIS. In period A there were 15 cases (3.1% of 486 screens) in 223 women, of which 2 (13%) were DCIS-one with microinvasion-neither detected by MRI. In period B there were 29 cases (3.3% of 877 screens) in 391 women, of which 10 (34%) were DCIS±microinvasion (p=0.04), all 10 detected by MRI but only one by mammography. No DCIS cases were detected by ultrasound or CBE. Specificity was lower in period B than in period A but acceptable. The ability to detect DCIS with screening MRI improves significantly with experience. MRI-guided biopsy capability is essential for a high-risk screening program. In experienced centers the increased sensitivity of MRI relative to mammography is at least as high for DCIS as it is for invasive breast cancer.

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PURPOSE: To evaluate three multicoil breast arrays for both conventional and SENSE-accelerated imaging. MATERIALS AND METHODS: Two commercially available 8-element coils and a prototype 16-element coil were compared. One 8-element array had adjustable coils located next to the breast tissue and the other had a fixed coil arrangement; both were designed to allow parallel imaging in the left-right direction. The 16-element coil was designed to have coil sensitivity variation in both the left-right and superior-inferior directions, and also had adjustable coils. Their performance was assessed in terms of signal-to-noise ratio (SNR), g-factor, and uniformity with a custom-built phantom. RESULTS: The 16-element array with adjustable coils provided the highest SNR, while the 8-element coil with a fixed coil arrangement had the best uniformity. All coils performed well for SENSE acceleration in the left-right direction. The 8-element coils did not have the capability for acceleration in the superior-inferior direction across the whole volume. The 16-element coil enabled acceleration in the superior-inferior direction in addition to the left-right direction. CONCLUSION: Smaller, adjustable coil elements located next to breast tissue can provide greater SNR than larger, fixed coil elements. A multicoil breast array with high intrinsic SNR and low g-factors enables high-quality parallel imaging.

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MR acoustic radiation force (ARF) imaging was developed for measuring tiSsue elastic properties using focused ultrasound to deliver a localized tissue motion. In this study, an imaging ultrasound transducer was mounted on the focused ultrasound transducer and ultrasound motion tracking was performed simultaneously to MR ARF imaging to validate the measurement results. In vivo studies on rabbit thigh muscle were performed and results showed a general agreement between the two modalities (slope=0.96 and R2=0.67). The temporal information by the ultrasound measurement indicates that the parameters in MR ARF imaging should be optimized according to the tissue type, acoustic power, and envelope and frequency of the ARF modulation.

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Breast tumor diagnosis requires both high spatial resolution to obtain information about tumor morphology and high temporal resolution to probe the kinetics of contrast uptake. Adaptive sampling of k-space allows images in dynamic contrast-enhanced (DCE)-magnetic resonance imaging (MRI) to be reconstructed at various spatial or temporal resolutions from the same dataset. However, conventional radial approaches have limited flexibility that restricts image reconstruction to predetermined resolutions. Golden-angle radial k-space sampling achieves flexibility in-plane with samples that are incremented by the golden angle, which fills two-dimensional (2D) k-space with radial spokes that have a relatively uniform angular distribution for any time interval. We extend this method to three-dimensional (3D) radial sampling, or 3D-Projection Reconstruction (3D-PR) using multidimensional golden means, which are derived from modified Fibonacci sequences by an eigenvalue approach. We quantitatively compare this technique to conventional 3D radial methods in terms of the fluctuation in error caused by undersampling artifacts, and show that the golden 3D-PR method can substantially improve the temporal stability of quantitative measurements made from dynamic images when compared to conventional 3D radial approaches of k-space sampling.

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OBJECTIVE: Sonographic correlation of breast MRI findings is often challenging. We present a preliminary in vivo feasibility study evaluating the degree of error of a new MRI-sonography coregistration system for showing MRI and sonographically visible breast lesions. CONCLUSION: In 10 patients with 13 lesions, the system was found to be an accurate means for targeting sonography to MRI of the same breast lesions.

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BACKGROUND: Several observational studies have shown that magnetic resonance imaging (MRI) is significantly more sensitive than mammography for screening women over age 25 at high risk for hereditary breast cancer; however, MRI is more costly and less specific than mammography. We sought to determine the extent to which the low sensitivity of mammography is due to greater breast density. METHODS: Breast density was evaluated for all patients on a high-risk screening study who were diagnosed with breast cancer between November 1997 and July 2006. Density was measured in two ways: qualitatively using the four categories characterized by the Breast Imaging Reporting and Data System and quantitatively using a computer-aided technique and classified as (a) 50% density. Comparison of sensitivity of mammography (and MRI) for each individual density category and after combining the highest two and lowest two density categories was done using Fisher's exact test. RESULTS: A total of 46 breast cancers [15 ductal carcinoma in situ (DCIS) and 31 invasive] were diagnosed in 45 women (42 with BRCA mutations). Mean age was 48.3 (range, 32-68) years. Overall, sensitivity of mammography versus MRI was 20% versus 87% for DCIS and 26% versus 90% for invasive cancer. There was a trend towards greater mammographic sensitivity for invasive cancer in women with fattier breasts compared with those with greater breast density (37-43% versus 8-12%; P = 0.1), but this trend was not seen for DCIS. CONCLUSION: It is necessary to add MRI to mammography for screening women with BRCA mutations even if their breast density is low.

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A single-point Dixon (SPD) fat/water separation method is proposed for breast dynamic contrast-enhanced MRI (DCE-MRI) in which field inhomogeneities and phase offsets measured prior to the injection of gadopentate dimeglumine (Gd-DTPA) are used to correct the postinjection images. A breast phantom study was conducted to demonstrate this technique, in which varying excess concentrations of Gd-DTPA (0-3 mM) were introduced into a 25-cm(3) breast lesion. The presence of excess Gd-DTPA in the lesion was found to create magnetic field perturbations of up to 0.35 microT per mM excess Gd-DTPA around the lesion. However, these perturbations had a negligible effect on the quality of the fat/water separation for Gd-DTPA concentrations in the range of, and exceeding, those observed in breast tumors following a standard 0.1 mmole/kg injection. Therefore, we conclude that the preinjection phase data is adequate for the correction of the postinjection images in breast exams.

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PURPOSE: To optimize a reordered k-space acquisition that applies intermittent fat saturation (FS) pulses to allow for a time-efficient reduction of fat signal in breast MR images, and compare it with an elliptic-centric biphasic FS method in terms of the degree of fat suppression and speed. MATERIALS AND METHODS: The behavior of the fat and water signals under the influence of the reordered sequence was characterized. This allowed us to optimize the flip angle and visualize the expected artifacts by deriving the point spread function (PSF) of the fat signal. We compared the two sequences by acquiring images with a varying number of FS pulses, with a corresponding difference in scan time. The quality of the images was assessed by comparison with images obtained with full fat suppression as measured by a root-mean-square (RMS) error metric. RESULTS: The reordered sequence allowed for an approximately twofold reduction in error compared to the biphasic sequence for the same scan time. With the reordered sequence and optimized scan parameters, we were able to reduce the time spent on fat suppression by as much as 99% with no discernible reduction in image quality. CONCLUSION: This method will allow robust fat suppression with virtually no extension in imaging time for dynamic contrast-enhanced (DCE)-MRI.

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A new interstitial breast localization marker is proposed which exhibits positive contrast in T1-weighted MRI, ultrasound and x-ray mammography. Unlike previous markers which provide MRI contrast on the basis of a susceptibility-induced signal void, this marker provides a clear positive contrast without any loss of signal or spatial distortion. The marker is composed of 400 microm diameter copper microspheres suspended in a Gd-DTPA-doped gel matrix. Optimal contrast in T1-weighted spoiled gradient recalled MRI was found to occur with the addition of 10 mM Gd-DTPA. Ultrasound contrast was generated on the basis of scattering from the copper microspheres. X-ray contrast was provided by the high x-ray attenuation properties of the copper microspheres. The study demonstrates potential suitability of the marker for use as a breast localization marker based on ex vivo studies of chicken breast.

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The benefit of screening with breast magnetic resonance (MR) imaging for certain patient populations at high risk for breast cancer, most notably patients with a genetic mutation in the BRCA1 or BRCA2 gene, has been established in numerous studies and is now becoming part of routine clinical practice. Despite the lower sensitivity of mammography compared with that of MR imaging, the former remains the standard of care for screening any patient population. In the BRCA1 and BRCA2 populations, the inferior sensitivity and specificity of ultrasonography (US) limit its role as a screening tool, but US remains a vital diagnostic tool because of its ability to provide guidance for biopsy of many suspicious lesions detected with MR imaging. Important features of a screening program with breast MR imaging include the following: optimization of the MR imaging technique, an awareness of the imaging features of invasive and noninvasive breast cancers detected with MR imaging, an understanding of the limitations of the various imaging modalities in both the initial screening and subsequent diagnostic work-up evaluations, and the requirement for MR imaging-guided biopsy.

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PURPOSE: To evaluate the degree of error of the authors' magnetic resonance (MR) imaging-guided needle localization system for biopsy of suspicious lesions visualized only with MR imaging, by using both prospectively recorded and retrospectively reviewed data, including MR imaging lesion coordinates as the reference standard, and to determine whether any lesion or breast characteristics affect this error. MATERIALS AND METHODS: Institutional review board approval, along with informed consent, was obtained as directed by the board. In 31 patients (age range, 34-64 years; mean age, 54.5 years), 38 wires were placed for 35 lesions by means of an MR-guided needle localization system with medial or lateral access and computer software assistance for needle placement calculation. Needle and wire placement error measurements were calculated before and after necessary placement correction, accounting for tissue shift in the z plane. The error was statistically correlated with MR imaging lesion variables, breast density, and histopathologic findings by means of univariate and multivariate linear regression analyses or two-tailed paired t test. Procedure times and the frequency of medial or lateral approaches were recorded. RESULTS: Eleven of 35 localizations (31%) were medial, and 24 of 35 (69%) were lateral. The mean total magnet time was 61.6 minutes, and the mean needle deployment time was 9 minutes (range, 4-17 minutes). Sixteen of 35 lesions (46%) were malignant (seven ductal carcinoma in situ, six invasive ductal, two invasive lobular, and one lymphoma). The mean uncorrected needle placement error was 1.3 mm (range, 0-6 mm) for the x plane, 2.4 mm (range, 0-6.5 mm) for the y plane, and 5.6 mm (range, 0-15.6 mm) for the z plane. Fourteen of 38 needles (37%) required repositioning for z-plane error. The corrected z-plane error improved to 3.2 mm (range, 0-10.0 mm). Factors that significantly increased the uncorrected error included tissue shift in the z plane (R = 0.7), small lesion size (R = -0.59), and fatty breast density (P = .029). CONCLUSION: The authors' system is accurate for performing MR-guided needle localizations for both medial and lateral approaches. Factors that increased the uncorrected needle placement error included small lesion size, fatty breast density, and tissue shift in the z plane.

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In this paper we propose a method for the nonrigid registration of contrast-enhanced dynamic sequences of magnetic resonance(MR) images. The algorithm has been developed with accuracy in mind, but also has a clinically viable execution time (i.e. a few minutes) as a goal. The algorithm is driven by multiresolution optical flow with the brightness consistency assumption relaxed, subject to a regularized best-fit within a family of transforms. The particular family of transforms we have employed uses a grid of control points and trilinear interpolation. We present validation results from a study simulating non-rigid deformation by a biomechanical model of the breast, with simulated uptake of a contrast agent. We further present results from applying the algorithm as part of a routine breast cancer screening protocol.

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RATIONALE AND OBJECTIVES: An in vivo evaluation of a new trimodality breast localization marker was performed with magnetic resonance imaging (MRI), ultrasound (US), x-ray, and histopathology. The evaluation of the marker in animal tests should help define its utility for surgical biopsy localization in humans. MATERIALS AND METHODS: Five rabbits were used and sacrificed at 2 days, 1 week, 2 weeks, 4 weeks, and 7 weeks after marker implantation. The marker placement and tissue biopsies were performed under US guidance. MRI, US, and x-ray imaging were performed to monitor the contrast of the marker, track marker migration. The biologic compatibility of the marker was demonstrated by histopathologic analysis. RESULTS: The contrast of the marker was clear and stable on each imaging modality over the 7-week study period. Acute inflammation was visible by 2 days after marker injection, with evidence of granulation tissue and angiogenesis at 2 weeks after implantation. A modest degree of chronic inflammation and angiogenesis remained evident at 4 weeks after procedure, and fibrosis persisted 7 weeks after procedure with no further tissue changes. These results suggest that the new marker is biocompatible and can remain interstitial for up to 7 weeks. Furthermore, very little marker migration was observed. On removal, the marker was found to be mechanically stable. CONCLUSION: This in vivo animal study demonstrates that the new marker may be appropriate for in vivo human testing and as an alternative to traditional wire localization currently used for breast surgery.

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