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OtherEvidence-based Clinical Medicine

Current Role of Magnetic Resonance Imaging in Breast Imaging: A Primer for the Primary Care Physician

Shinil K. Shah, Shiwan K. Shah and Kathleen V. Greatrex
The Journal of the American Board of Family Practice November 2005, 18 (6) 478-490; DOI: https://doi.org/10.3122/jabfm.18.6.478
Shinil K. Shah
BS
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Shiwan K. Shah
BS
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Kathleen V. Greatrex
MD
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    MR scanning of a patient using a dedicated breast coil

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    Table 1.

    Major Applications of MRI in Breast Imaging

    ApplicationsMEDLINE Search Terms
    Staging of breast cancer (including determining involvement of pectoral musculature)Magnetic resonance imaging AND breast cancer staging
    Determination of recurrent/residual disease after treatmentMagnetic resonance imaging AND breast cancer AND residual disease
    Determination of occult breast cancer (especially in patients with negative mammograms)Magnetic resonance imaging AND breast cancer AND unknown primary
    Possible use as a screening tool in patients at high risk for breast cancerMagnetic resonance imaging AND breast cancer AND high risk
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    Table 2.

    MRI in Staging of Breast Cancer

    StudyType of StudyStudy PopulationNMajor Findings/Comments
    Boetes et al.23RetrospectivePatients with invasive lobular carcinoma treated surgically34 (36 cases of breast cancer)False negative rate for MRI was 0% compared with 3% and 14% for US and XRM, respectively; when 2 radiologists retrospectively reviewed the exam results, the percentage of correctly identified size of cancer was 47% and 75% for MRI (r = 0.81, P < .01); this was the most accurate and most highly correlated method
    Schelfout et al.17ProspectiveWomen with lesions on XRM, US, and/or CBE21296%, 37%, and 41% of multifocal disease was detected by MRI, XRM, and US, respectively; 95%, 18%, and 9% of multicentric disease was detected by MRI, XRM, and US, respectively; 100% of bilateral breast cancers were seen on MRI; 56% of bilateral breast cancers were seen on XRM and US
    Van Goethem et al.24ProspectivePatients with dense breasts planning to undergo surgery6765/67 patients had breast cancer confirmed pathologically; MRI was 98% sensitive for initial lesion compared with 83% and 70.8% for XRM and US, respectively; extent of cancer was underestimated by 12.5% of MRI results as opposed to 37% and 40% for XRM and US results, respectively; multifocal/multicentric disease was picked up 100% of the time by MRI as opposed to 35% and 30% of XRM and US, respectively
    Bedrosian et al.18RetrospectivePatients diagnosed with invasive breast cancer who had MRI preoperatively267MRI was 95% sensitive for detecting primary breast cancer; planned management of 26% of patients (N = 69) were changed due to MRI results—in 49/69 (71%) of the patients, postsurgical pathology confirmed that the change in management was appropriate
    Rieber et al.28ProspectivePatients suspected of having breast malignancy based on results of XRM, US, or CBE43Sensitivity of MR mammography for diagnosis of primary cancer, contralateral cancer, and multifocal disease was 100%, 100%, and 95.2%; similar values were 93%, 100%, and 92.5% for PET, respectively
    Fischer et al.20ProspectivePatients with breast abnormalities after XRM, CBE, PE, and US46366 patients (14.3%) had their planned therapy accurately changed as a result of MRI of the breast with 16 patients (3.5%) undergoing unneeded open biopsy
    Esserman et al.21ProspectivePatients with breast cancer with planned surgical correction57 (58 cases of breast cancer)Preoperative MRI identified degree of disease accurately in 54/58 cases of breast cancer; anatomic detail identified on MRI was accurate 98% of the time whereas anatomic detail identified on XRM was accurate in 55% of cases
    Rodenko et al.22RetrospectivePatients with infiltrating lobular carcinoma who had MRI and XRM performed preoperatively20Postoperative pathology correlated with preoperative MRI findings in 85% of patients; The correlation with preoperative XRM was 32% (P < .0001)
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    Table 3.

    MRI in the Evaluation of Residual Disease

    StudyType of StudyStudy PopulationNMajor Findings/Comments
    Yeh et al.25ProspectivePatients with stage IIb/III breast cancer undergoing neoadjuvant chemotherapy (doxorubicin and paclitaxel)31Correlation with pathology
    Equal to pathology/underestimate/overestimate
        MRI: 71%/23%/6%
        XRM: 26%/52%/23%
        US: 35%/52%/13%
        MRI was best correlated with pathology
        (P < .002)
    Chen et al.26ProspectivePatients with locally advanced breast cancer receiving neoadjuvant therapy (adriamycin, cytoxan, and paclitaxel)15MRI tended to overestimate tumor response; for partial non-responders MRI correlated with pathology 0% of the time compared with 17% for CBE and 83% for PET; however, for responders, MRI correlated with pathology 90% of the time, with 70% correlation for CBE and 90% for PET; MRI size measurements of residual tumors did correlate with pathology (coefficient 0.7 compared with −0.06 for CBE)
    Denis et al.27ProspectivePatients with locally advanced breast cancer receiving neoadjuvant therapy with either 5–5-fluorouracil/epirubicin/ cyclophosphamide; docetaxel only, or docetaxel with epirubicin40Correlation coefficient of MRI measurements with pathology: 5-fluorouracil/E/C: 0.89, DXL: 0.64, DXL/E: 0.16 MRI overestimated tumor response in DXL-based groups, which was believed to be due to antiangiogenic effect of DXL, which would impair MRI contrast enhancement; this was supported by the fact that DXL-based groups had residual disease of microscopic nests of tumor cells on pathology as opposed to single nodular lesions
    Tozaki et al.28ProspectivePatients with locally advanced breast cancer (IIb/III) undergoing neoadjuvant chemotherapy19Accuracy (deviation from pathology of less than 2 mm) of late phase CT and MRI scans (scan 4 minutes after contrast injection) compared with pathology was up to 90% for DCIS and replaced (diffuse pre-NAC contrast enhancement) lesions and 88% for nonreplaced (localized CE) lesions; early phase scans were 0% accurate for DCIS/replaced and 75% accurate for nonreplaced lesions
    Bodini et al.29ProspectivePatients with T2 to 4, N0 M0 breast cancer treated with 3 to 4 cycles of epirubicin79Clinical response correlation with pathology correlation coefficients were 0.72 for MRI and 0.68 for CBE
    Warren et al.30RetrospectivePatients undergoing neoadjuvant therapy67MRI was more sensitive and specific for assessment of complete or partial response (100% and 80%) than conventional assessment methods (CAM), including XRM, US, and CBE (98% and 50%); agreement with pathology was marginally higher in MRI compared with CAM (81% compared to 68%, P = .09); MRI increased diagnostic knowledge in 70% of patients, and increased diagnostic confidence in 52%; however, MRI did not change treatment plan, decreased confidence in 20% of patients, and decreased knowledge in 17%; MRI tended to overestimate response
    Lee et al.31RetrospectivePatients who had excisional biopsy who required definitive surgery, eg, because of positive margins/residual disease and were candidates for breast conservation80MRI sensitivity and specificity for residual disease was 61.2% and 69.7%, respectively; additional lesions were detected by imaging of which 10 were only seen on MRI; of these, 5 were benign, 5 were malignant; MRI changed management of patients in 29% of the cases, because of additional lesions found; whether this led to improved patient outcomes is not known
    Rosen et al.32RetrospectivePatients with locally advanced breast cancer treated with neoadjuvant therapy (paclitaxel, doxorubicin, and breast hyperthermia)21Correlation with pathology equal to pathology/underestimate/overestimate MRI: 57%/10%/33% correlation coefficients were 0.74 for MRI and 0.65 (statistically nonsignificant trend); in contrast to some of the other studies, MRI tended to overestimate the residual tumor (ie, underestimate response)
    Hwang et al.33RetrospectivePatients with histologically confirmed diagnosis of DCIS51MRI was 97% sensitive and 58% specific for detecting residual disease compared with histology; the sensitivity was significantly better than the sensitivity of XRM for residual disease; in addition MRI had a significantly higher NPV compared to XRM
    Belli et al.34ProspectivePatients with locally advanced breast cancer being treated with neoadjuvant chemotherapy45MRI had a 90.2% sensitivity and a 100% specificity for residual disease
    Cheung et al.35ProspectivePatients with locally advanced breast cancer being treated with neoadjuvant chemotherapy33Residual tumor on MRI correlated with microscopic findings (correlation coefficient = 0.982, P < .001)
    Partridge et al.36ProspectivePatients with invasive breast cancer undergoing neoadjuvant therapy with doxorubicin and cyclophosphamide52Decreased tumor enhancement prechemotherapy and postchemotherapy (210% vs 166%, P < .001); MRI had correlation coefficient of 0.89 compared with pathology whereas clinical examination had coefficient of 0.60
    Kawashima et al.37ProspectivePatients who underwent excisional biopsy of breast lesion50MRI in detection of residual disease: sensitivity 66%; specificity 81%; PPV 72%; NPV 83%; accuracy 63%
    Drew et al.38ProspectivePatients with locally advanced breast cancer receiving neoadjuvant therapy17Dynamic CE MRI was 100% accurate in assessing residual disease; CBE and XRM were not sensitivity/specificity/PPV/NPV CBE: 50%/86%/83%/55% XRM: 90%/57%/75%/80%
    Weatherall et al.39RetrospectivePatients with breast cancer with chemotherapy prior to surgery20MRI demonstrated a correlation with pathology (coefficient = 0.93); coefficients for CBE and XRM were 0.72 and 0.63, respectively
    Frei et al.40RetrospectivePatients with excisional biopsy68MRI sensitivity/specificity/PPV/NPV >7 days postbiopsy: 89%/52%/81%/69% >14 days postbiopsy: 88%/58%/82%/69% >21 days postbiopsy: 91%/69%/88%/75% >28 days postbiopsy: 92%/75%/92%/75% >35 days postbiopsy: 95%/75%/91%/86% >42 days postbiopsy: 94%/75%/89%/86%The peak values for PPV and plateau for specificity occurs at >28 days, after which the improvement is not as much; therefore, this may be the best time to perform the MRI as the PPV of positive margins in this study was 69% compared to 92% for MRI at day 28, which may lead to breast-conserving surgery
    Trecate et al.41ProspectivePatients with locally advanced breast cancer receiving chemotherapy30MRI: sensitivity: 96%; specificity: 75%; PPV: 92.5%; NPV 66%; accuracy 90%
    Orel et al.42ProspectivePatients who underwent excisional biopsy47MRI had PPV of 82% and NPV of 61%; false negatives possibly secondary to postsurgical changes
    Soderstrom et al.43)ProspectivePatients who underwent excisional biopsies19MRI had an 84% accuracy in determining whether residual tumor was present in patients postexcisional biopsy
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    Table 4.

    MRI in Occult Breast Cancer

    StudyType of StudyStudy PopulationNMean Age/RangeMajor Findings/Comments
    Olson et al.45ProspectiveWomen with unknown primary and metastatic axillary adenocarcinoma; initial XRM, US, or PE was not diagnostic of malignancy4058(+) MRI correlated with breast tumor in 81% of cases overall; initial XRM, US, or PE was not diagnostic of malignancy
    Henry-Tillman RS et al. (Dec 1999) (54)RetrospectivePatients with unknown primary, (+) axillary/supraclavicular lymphadenopathy, (−) XRM/CBE, and (+) MRI1036 to 68MRI was 100% accurate when correlated with pathology; 80% (N = 8) were (+) and primary breast CA was confirmed; 20% (N = 2) were negative and other primaries (ovarian CA and lymphoma) were identified
    Orel SG et al. (Aug 1999) (55)ProspectivePatients with (+) axillary node metastasis, negative PE and XRM, and unknown primary2249Breast cancer was detected as the primary in 86% (N = 19) of cases; 17 were confirmed by pathology; 2 resolved on MRI follow-up during chemotherapy
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    Table 5.

    MRI as a Screening Tool in High Risk Women

    StudyType of StudyStudy PopulationNMean Age/RangeMajor Findings/Comments
    Leach et al.55ProspectiveWomen at high risk for breast cancer (BRCA 1, 2, or TP53 mutation, 1st degree relative with mutation, family history of breast/ovarian CA, family history of Li-Fraumeni syndrome)64931 to 55Sensitivity for CE MRI and XRM was 77% and 40%, respectively; specificity for CE MRI and XRM was 81% and 93%, respectively; sensitivity and specificity for both methods combined was 94% and 77%, respectively; sensitivity of CE MRI for BRCA 1 and BRCA 2 were 92% and 58%, respectively
    Lehman et al.56ProspectiveWomen ≥25 with high familial or genetic risk of breast cancer367401.1% of patients screened with MRI had breast cancer by pathology as opposed to 0.3% by XRM (difference not statistically significant); PPV of biopsies performed as a result of MRI was 17% (4/24); PPV of biopsies performed as a result of XRM was 25% (1/4)
    Sim et al.58RetrospectiveWomen who were at least at 15% greater risk for breast cancer (Claus model)179Sensitivity for MRI, XRM, and US were 93.3%, 83.3%, and 53.9%, respectively; specificity for MRI, XRM, and US were 63.6%, 65.5%, and 85.7%, respectively; the sensitivity and specificity for combined XRM and US was 92.9% and 62.5%, respectively
    Kriege et al.50ProspectiveWomen who were at least at 15% greater risk for breast cancer due to familial or genetic factors (Claus model)190940Sensitivity for MRI in detecting invasive breast cancer as opposed to CBE and XRM was 79.5%, 17.9%, and 33.3%, respectively; specificity for MRI, CBE, and XRM was 89.8%, 98.1%, and 95.0%, respectively
    Morris et al.54RetrospectiveWomen at high risk for breast cancer (past history, family history, LCIS, atypia) with negative XRM367504% of screened patients had breast cancer by pathology (57% were DCIS); percentage was higher in those women with past and family history (8%), PPV 50%; PPV of biopsy was 24%
    Warner et al.49ProspectiveWomen who were carriers of BRCA 1 and/or BRCA 223625 to 65Sensitivity for MRI as opposed to XRM, US, and CBE were 77%, 36% (P = .02), 33% (P = .006), and 9.1%, respectively; specificity for MRI, XRM, US, and CBE were 95.4%, 99.8%, 96%, and 99.3%, respectively; when all modalities were combined there was a sensitivity of 95% as opposed to 45% with XRM and CBE combined
    Podo et al.57ProspectiveWomen with confirmed BRCA 1 or BRCA 2 mutations or with a 1 in 2 chance of having the mutation10555.38 breast cancers were identified (all by CE MRI); only 1 was detected by XRM and US; total incidence of breast cancer was 7.6%
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The Journal of the American Board of Family Practice: 18 (6)
The Journal of the American Board of Family Practice
Vol. 18, Issue 6
November-December 2005
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Current Role of Magnetic Resonance Imaging in Breast Imaging: A Primer for the Primary Care Physician
Shinil K. Shah, Shiwan K. Shah, Kathleen V. Greatrex
The Journal of the American Board of Family Practice Nov 2005, 18 (6) 478-490; DOI: 10.3122/jabfm.18.6.478

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Current Role of Magnetic Resonance Imaging in Breast Imaging: A Primer for the Primary Care Physician
Shinil K. Shah, Shiwan K. Shah, Kathleen V. Greatrex
The Journal of the American Board of Family Practice Nov 2005, 18 (6) 478-490; DOI: 10.3122/jabfm.18.6.478
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