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The frequency of missed breast cancers in women participating in a high-risk MRI screening program

PURPOSE: To evaluate the frequency of missed cancers on breast MRI in women participating in a high-risk screening program. METHODS: Patient files from women who participated in an increased risk mammography and MRI screening program (2003–2014) were coupled to the Dutch National Cancer Registry. Fo...

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Autores principales: Vreemann, S., Gubern-Merida, A., Lardenoije, S., Bult, P., Karssemeijer, N., Pinker, K., Mann, R. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945731/
https://www.ncbi.nlm.nih.gov/pubmed/29383629
http://dx.doi.org/10.1007/s10549-018-4688-z
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author Vreemann, S.
Gubern-Merida, A.
Lardenoije, S.
Bult, P.
Karssemeijer, N.
Pinker, K.
Mann, R. M.
author_facet Vreemann, S.
Gubern-Merida, A.
Lardenoije, S.
Bult, P.
Karssemeijer, N.
Pinker, K.
Mann, R. M.
author_sort Vreemann, S.
collection PubMed
description PURPOSE: To evaluate the frequency of missed cancers on breast MRI in women participating in a high-risk screening program. METHODS: Patient files from women who participated in an increased risk mammography and MRI screening program (2003–2014) were coupled to the Dutch National Cancer Registry. For each cancer detected, we determined whether an MRI scan was available (0–24 months before cancer detection), which was reported to be negative. These negative MRI scans were in consensus re-evaluated by two dedicated breast radiologists, with knowledge of the cancer location. Cancers were scored as invisible, minimal sign, or visible. Additionally, BI-RADS scores, background parenchymal enhancement, and image quality (IQ; perfect, sufficient, bad) were determined. Results were stratified by detection mode (mammography, MRI, interval cancers, or cancers in prophylactic mastectomies) and patient characteristics (presence of BRCA mutation, age, menopausal state). RESULTS: Negative prior MRI scans were available for 131 breast cancers. Overall 31% of cancers were visible at the initially negative MRI scan and 34% of cancers showed a minimal sign. The presence of a BRCA mutation strongly reduced the likelihood of visible findings in the last negative MRI (19 vs. 46%, P < 0.001). Less than perfect IQ increased the likelihood of visible findings and minimal signs in the negative MRI (P = 0.021). CONCLUSION: This study shows that almost one-third of cancers detected in a high-risk screening program are already visible at the last negative MRI scan, and even more in women without BRCA mutations. Regular auditing and double reading for breast MRI screening is warranted.
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spelling pubmed-59457312018-05-15 The frequency of missed breast cancers in women participating in a high-risk MRI screening program Vreemann, S. Gubern-Merida, A. Lardenoije, S. Bult, P. Karssemeijer, N. Pinker, K. Mann, R. M. Breast Cancer Res Treat Clinical Trial PURPOSE: To evaluate the frequency of missed cancers on breast MRI in women participating in a high-risk screening program. METHODS: Patient files from women who participated in an increased risk mammography and MRI screening program (2003–2014) were coupled to the Dutch National Cancer Registry. For each cancer detected, we determined whether an MRI scan was available (0–24 months before cancer detection), which was reported to be negative. These negative MRI scans were in consensus re-evaluated by two dedicated breast radiologists, with knowledge of the cancer location. Cancers were scored as invisible, minimal sign, or visible. Additionally, BI-RADS scores, background parenchymal enhancement, and image quality (IQ; perfect, sufficient, bad) were determined. Results were stratified by detection mode (mammography, MRI, interval cancers, or cancers in prophylactic mastectomies) and patient characteristics (presence of BRCA mutation, age, menopausal state). RESULTS: Negative prior MRI scans were available for 131 breast cancers. Overall 31% of cancers were visible at the initially negative MRI scan and 34% of cancers showed a minimal sign. The presence of a BRCA mutation strongly reduced the likelihood of visible findings in the last negative MRI (19 vs. 46%, P < 0.001). Less than perfect IQ increased the likelihood of visible findings and minimal signs in the negative MRI (P = 0.021). CONCLUSION: This study shows that almost one-third of cancers detected in a high-risk screening program are already visible at the last negative MRI scan, and even more in women without BRCA mutations. Regular auditing and double reading for breast MRI screening is warranted. Springer US 2018-01-31 2018 /pmc/articles/PMC5945731/ /pubmed/29383629 http://dx.doi.org/10.1007/s10549-018-4688-z Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Clinical Trial
Vreemann, S.
Gubern-Merida, A.
Lardenoije, S.
Bult, P.
Karssemeijer, N.
Pinker, K.
Mann, R. M.
The frequency of missed breast cancers in women participating in a high-risk MRI screening program
title The frequency of missed breast cancers in women participating in a high-risk MRI screening program
title_full The frequency of missed breast cancers in women participating in a high-risk MRI screening program
title_fullStr The frequency of missed breast cancers in women participating in a high-risk MRI screening program
title_full_unstemmed The frequency of missed breast cancers in women participating in a high-risk MRI screening program
title_short The frequency of missed breast cancers in women participating in a high-risk MRI screening program
title_sort frequency of missed breast cancers in women participating in a high-risk mri screening program
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945731/
https://www.ncbi.nlm.nih.gov/pubmed/29383629
http://dx.doi.org/10.1007/s10549-018-4688-z
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