Rapid MRI of the breast in evaluating lesions discovered on screening
Background In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader...
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Published in | The breast journal Vol. 24; no. 6; pp. 986 - 991 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.11.2018
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Abstract | Background
In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader time. In this study, we evaluate a rapid MRI protocol for breast cancer screening within a breast screening population.
Methods
A series of 100 MRI studies performed in a high‐risk breast cancer population were selected, ensuring a mix of malignant and benign pathology and normal cases. These were presented as full and abbreviated MRI protocols to 3 breast‐trained radiologists. Each case was evaluated for Breast Imaging Reporting and Data Systems (BIRADS) category and the presence or absence of cancer. The time taken to complete and interpret each study was also recorded.
Results
Of the 100 cases, 17 were of histopathology‐proven invasive carcinoma, 6 were ductal carcinoma in situ, 33 were benign, and 44 were normal cases. Sensitivity using the rapid protocol was 69.6% (CI: 47.1‐86.8) vs 83% (CI: 61.2‐95.1) using the full protocol. Specificity using the rapid protocol was 77.9% (CI: 67.0‐86.6) vs 83% (CI: 61.2‐95.1) using the full protocol. Intra‐observer agreement of BIRADS category and cancer detection was very good (0.82‐0.93 weighted Kappa and 0.81‐0.9 weighted Kappa, respectively). Inter‐observer variability of BIRADS category and cancer detection was moderate (0.54‐0.59 and 0.53‐0.58, respectively).
Conclusion
Our study suggests that a rapid MRI protocol is comparable in performance to that of a standard MRI protocol. In addition, breast imagers are unlikely to change their BIRADS assessment of a study based on the additional sequences provided by the lengthier study. The use of a rapid MRI protocol can improve accessibility, thus making breast MRI a more utilized tool for breast cancer screening. |
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AbstractList | Background
In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader time. In this study, we evaluate a rapid MRI protocol for breast cancer screening within a breast screening population.
Methods
A series of 100 MRI studies performed in a high‐risk breast cancer population were selected, ensuring a mix of malignant and benign pathology and normal cases. These were presented as full and abbreviated MRI protocols to 3 breast‐trained radiologists. Each case was evaluated for Breast Imaging Reporting and Data Systems (BIRADS) category and the presence or absence of cancer. The time taken to complete and interpret each study was also recorded.
Results
Of the 100 cases, 17 were of histopathology‐proven invasive carcinoma, 6 were ductal carcinoma in situ, 33 were benign, and 44 were normal cases. Sensitivity using the rapid protocol was 69.6% (CI: 47.1‐86.8) vs 83% (CI: 61.2‐95.1) using the full protocol. Specificity using the rapid protocol was 77.9% (CI: 67.0‐86.6) vs 83% (CI: 61.2‐95.1) using the full protocol. Intra‐observer agreement of BIRADS category and cancer detection was very good (0.82‐0.93 weighted Kappa and 0.81‐0.9 weighted Kappa, respectively). Inter‐observer variability of BIRADS category and cancer detection was moderate (0.54‐0.59 and 0.53‐0.58, respectively).
Conclusion
Our study suggests that a rapid MRI protocol is comparable in performance to that of a standard MRI protocol. In addition, breast imagers are unlikely to change their BIRADS assessment of a study based on the additional sequences provided by the lengthier study. The use of a rapid MRI protocol can improve accessibility, thus making breast MRI a more utilized tool for breast cancer screening. BackgroundIn Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader time. In this study, we evaluate a rapid MRI protocol for breast cancer screening within a breast screening population.MethodsA series of 100 MRI studies performed in a high‐risk breast cancer population were selected, ensuring a mix of malignant and benign pathology and normal cases. These were presented as full and abbreviated MRI protocols to 3 breast‐trained radiologists. Each case was evaluated for Breast Imaging Reporting and Data Systems (BIRADS) category and the presence or absence of cancer. The time taken to complete and interpret each study was also recorded.ResultsOf the 100 cases, 17 were of histopathology‐proven invasive carcinoma, 6 were ductal carcinoma in situ, 33 were benign, and 44 were normal cases. Sensitivity using the rapid protocol was 69.6% (CI: 47.1‐86.8) vs 83% (CI: 61.2‐95.1) using the full protocol. Specificity using the rapid protocol was 77.9% (CI: 67.0‐86.6) vs 83% (CI: 61.2‐95.1) using the full protocol. Intra‐observer agreement of BIRADS category and cancer detection was very good (0.82‐0.93 weighted Kappa and 0.81‐0.9 weighted Kappa, respectively). Inter‐observer variability of BIRADS category and cancer detection was moderate (0.54‐0.59 and 0.53‐0.58, respectively).ConclusionOur study suggests that a rapid MRI protocol is comparable in performance to that of a standard MRI protocol. In addition, breast imagers are unlikely to change their BIRADS assessment of a study based on the additional sequences provided by the lengthier study. The use of a rapid MRI protocol can improve accessibility, thus making breast MRI a more utilized tool for breast cancer screening. In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader time. In this study, we evaluate a rapid MRI protocol for breast cancer screening within a breast screening population. A series of 100 MRI studies performed in a high-risk breast cancer population were selected, ensuring a mix of malignant and benign pathology and normal cases. These were presented as full and abbreviated MRI protocols to 3 breast-trained radiologists. Each case was evaluated for Breast Imaging Reporting and Data Systems (BIRADS) category and the presence or absence of cancer. The time taken to complete and interpret each study was also recorded. Of the 100 cases, 17 were of histopathology-proven invasive carcinoma, 6 were ductal carcinoma in situ, 33 were benign, and 44 were normal cases. Sensitivity using the rapid protocol was 69.6% (CI: 47.1-86.8) vs 83% (CI: 61.2-95.1) using the full protocol. Specificity using the rapid protocol was 77.9% (CI: 67.0-86.6) vs 83% (CI: 61.2-95.1) using the full protocol. Intra-observer agreement of BIRADS category and cancer detection was very good (0.82-0.93 weighted Kappa and 0.81-0.9 weighted Kappa, respectively). Inter-observer variability of BIRADS category and cancer detection was moderate (0.54-0.59 and 0.53-0.58, respectively). Our study suggests that a rapid MRI protocol is comparable in performance to that of a standard MRI protocol. In addition, breast imagers are unlikely to change their BIRADS assessment of a study based on the additional sequences provided by the lengthier study. The use of a rapid MRI protocol can improve accessibility, thus making breast MRI a more utilized tool for breast cancer screening. In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader time. In this study, we evaluate a rapid MRI protocol for breast cancer screening within a breast screening population.BACKGROUNDIn Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been emerging as an instrument for breast screening. However, its utilization is limited by increased relative cost and increased reader time. In this study, we evaluate a rapid MRI protocol for breast cancer screening within a breast screening population.A series of 100 MRI studies performed in a high-risk breast cancer population were selected, ensuring a mix of malignant and benign pathology and normal cases. These were presented as full and abbreviated MRI protocols to 3 breast-trained radiologists. Each case was evaluated for Breast Imaging Reporting and Data Systems (BIRADS) category and the presence or absence of cancer. The time taken to complete and interpret each study was also recorded.METHODSA series of 100 MRI studies performed in a high-risk breast cancer population were selected, ensuring a mix of malignant and benign pathology and normal cases. These were presented as full and abbreviated MRI protocols to 3 breast-trained radiologists. Each case was evaluated for Breast Imaging Reporting and Data Systems (BIRADS) category and the presence or absence of cancer. The time taken to complete and interpret each study was also recorded.Of the 100 cases, 17 were of histopathology-proven invasive carcinoma, 6 were ductal carcinoma in situ, 33 were benign, and 44 were normal cases. Sensitivity using the rapid protocol was 69.6% (CI: 47.1-86.8) vs 83% (CI: 61.2-95.1) using the full protocol. Specificity using the rapid protocol was 77.9% (CI: 67.0-86.6) vs 83% (CI: 61.2-95.1) using the full protocol. Intra-observer agreement of BIRADS category and cancer detection was very good (0.82-0.93 weighted Kappa and 0.81-0.9 weighted Kappa, respectively). Inter-observer variability of BIRADS category and cancer detection was moderate (0.54-0.59 and 0.53-0.58, respectively).RESULTSOf the 100 cases, 17 were of histopathology-proven invasive carcinoma, 6 were ductal carcinoma in situ, 33 were benign, and 44 were normal cases. Sensitivity using the rapid protocol was 69.6% (CI: 47.1-86.8) vs 83% (CI: 61.2-95.1) using the full protocol. Specificity using the rapid protocol was 77.9% (CI: 67.0-86.6) vs 83% (CI: 61.2-95.1) using the full protocol. Intra-observer agreement of BIRADS category and cancer detection was very good (0.82-0.93 weighted Kappa and 0.81-0.9 weighted Kappa, respectively). Inter-observer variability of BIRADS category and cancer detection was moderate (0.54-0.59 and 0.53-0.58, respectively).Our study suggests that a rapid MRI protocol is comparable in performance to that of a standard MRI protocol. In addition, breast imagers are unlikely to change their BIRADS assessment of a study based on the additional sequences provided by the lengthier study. The use of a rapid MRI protocol can improve accessibility, thus making breast MRI a more utilized tool for breast cancer screening.CONCLUSIONOur study suggests that a rapid MRI protocol is comparable in performance to that of a standard MRI protocol. In addition, breast imagers are unlikely to change their BIRADS assessment of a study based on the additional sequences provided by the lengthier study. The use of a rapid MRI protocol can improve accessibility, thus making breast MRI a more utilized tool for breast cancer screening. |
Author | Jong, Roberta Betel, Carrie Skarpathiotakis, Mia Hack, Kalesha Thornhill, Rebecca Curpen, Belinda Richmond, Lara Seppala, Nicholas Fallah Rastegar, Rashin |
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CitedBy_id | crossref_primary_10_1155_2022_8705531 crossref_primary_10_1016_j_crad_2020_08_036 crossref_primary_10_2463_mrms_rev_2024_0158 crossref_primary_10_1016_j_ejro_2020_100307 crossref_primary_10_1148_radiol_221822 crossref_primary_10_5114_pjr_2024_135474 crossref_primary_10_1007_s00330_022_08622_9 crossref_primary_10_31083_j_ceog5006115 crossref_primary_10_1016_j_crad_2020_08_032 crossref_primary_10_17656_jsmc_10228 |
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In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI... In Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI has been... BackgroundIn Canada, breast MRI has traditionally been reserved for evaluation of disease extent in patients with known breast malignancy. More recently, MRI... |
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SubjectTerms | abbreviated protocol Benign Breast cancer Breast Neoplasms - diagnostic imaging Breast Neoplasms - pathology Cancer Cancer screening Data systems Female Health risks Histopathology Humans Invasiveness Lesions Magnetic resonance imaging Magnetic Resonance Imaging - methods Malignancy Mass Screening - methods Medical screening MRI Observer Variation screening Sensitivity and Specificity Sequences Time Factors |
Title | Rapid MRI of the breast in evaluating lesions discovered on screening |
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