Abstract
BackgroundIn an effort to reduce necessary acquisition time to perform molecular breast imaging (MBI), we compared diagnostic performance of MBI performed with standard 10-min-per-view acquisitions and half-time 5-min-per-view acquisitions, with and without wide beam reconstruction (WBR) processing.MethodsEighty-two bilateral, two-view MBI studies were reviewed. Studies were performed with 300 MBq Tc-99 m sestamibi and a direct conversion molecular breast imaging (DC-MBI) system. Acquisitions were 10 min-per-view; the first half of each was extracted to create 5-min-per-view datasets, and WBR processing was applied.The 10-min-, 5-min-, and 5-min-per-view WBR studies were independently interpreted in a randomized, blinded fashion by two radiologists. Assessments of 1 to 5 were assigned; 4 and 5 were considered test positive. Background parenchymal uptake, lesion type, distribution of non-mass lesions, lesion intensity, and image quality were described.ResultsConsidering detection of all malignant and benign lesions, 5 min-per-view MBI had lower sensitivity (mean of 70% vs. 85% (p ≤ 0.04) for two readers) and lower area under curve (AUC) (mean of 92.7 vs. 99.6, p ≤ 0.01) but had similar specificity (p = 1.0). WBR processing did not alter sensitivity, specificity, or AUC obtained at 5 min-per-view.Overall agreement in final assessment between 5-min-per-view and 10-min-per-view acquisition types was near perfect (κ = 0.82 to 0.89); however, fair to moderate agreement was observed for assessment category 3 (probably benign) (κ = 0.24 to 0.48). Of 33 malignant lesions, 6 (18%) were changed from assessment of 4 or 5 with 10-min-per-view MBI to assessment of 3 with 5-min-per-view MBI. Image quality of 5-min-per-view studies was reduced compared to 10-min-per-view studies for both readers (3.24 vs. 3.98, p < 0.0001 and 3.60 vs. 3.91, p < 0.0001). WBR processing improved image quality for one reader (3.85 vs. 3.24, p < 0.0001).ConclusionsAlthough similar radiologic interpretations were obtained with 10-min- and 5-min-per-view DC-MBI, resulting in substantial agreement in final assessment, notable exceptions were found: (1) perceived image quality at 5 min-per-view was lower than that for 10-min-per-view studies and (2) in a number of cases, assessment was downgraded from a recommendation of biopsy to that of short interval follow-up.
Highlights
In an effort to reduce necessary acquisition time to perform molecular breast imaging (MBI), we compared diagnostic performance of MBI performed with standard 10-min-per-view acquisitions and half-time 5-min-per-view acquisitions, with and without wide beam reconstruction (WBR) processing
Following the implementation of a registered highsensitivity collimation designed for dual-head direct conversion molecular breast imaging (DC-MBI) systems [6] and a cadmium zinc telluride (CZT)-specific energy acceptance window to capture additional photopeak counts [7], DCMBI is routinely performed at our institution with injection of approximately 220 to 300 MBq (6 to 8 mCi) Tc-99 m sestamibi, which corresponds to an effective radiation dose of 1.8 to 2.4 mSv
In the 82 patients, reference standard was positive for breast cancer in 33 and negative in 49
Summary
In an effort to reduce necessary acquisition time to perform molecular breast imaging (MBI), we compared diagnostic performance of MBI performed with standard 10-min-per-view acquisitions and half-time 5-min-per-view acquisitions, with and without wide beam reconstruction (WBR) processing. Following the implementation of a registered highsensitivity collimation designed for dual-head DC-MBI systems [6] and a CZT-specific energy acceptance window to capture additional photopeak counts [7], DCMBI is routinely performed at our institution with injection of approximately 220 to 300 MBq (6 to 8 mCi) Tc-99 m sestamibi, which corresponds to an effective (whole-body) radiation dose of 1.8 to 2.4 mSv. A similar cancer detection rate of 12.0 per 1,000 has been obtained with addition of this low-dose MBI to screening mammography in women with dense breasts [8]. In an effort to keep doses from medical imaging as low as reasonably achievable and to promote acceptance of MBI in the screening environment, further dose reductions may be desirable
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