The supplemental value of mammographic screening over breast MRI alone in BRCA2 mutation carriers.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 12 12 2019
accepted: 10 04 2020
pubmed: 26 4 2020
medline: 20 1 2021
entrez: 26 4 2020
Statut: ppublish

Résumé

BRCA2 mutation carriers are offered annual breast screening with MRI and mammography. The aim of this study was to investigate the supplemental value of mammographic screening over MRI screening alone. In this multicenter study, proven BRCA2 mutation carriers, who developed breast cancer during screening using both digital mammography and state-of-art breast MRI, were identified. Clinical data were reviewed to classify cases in screen-detected and interval cancers. Imaging was reviewed to assess the diagnostic value of mammography and MRI, using the Breast Imaging and Data System (BI-RADS) classification allocated at the time of diagnosis. From January 2003 till March 2019, 62 invasive breast cancers and 23 ductal carcinomas in situ were diagnosed in 83 BRCA2 mutation carriers under surveillance. Overall screening sensitivity was 95.2% (81/85). Four interval cancers occurred (4.7% (4/85)). MRI detected 73 of 85 breast cancers (sensitivity 85.8%) and 42 mammography (sensitivity 49.9%) (p < 0.001). Eight mammography-only lesions occurred. In 1 of 17 women younger than 40 years, a 6-mm grade 3 DCIS, retrospectively visible on MRI, was detected with mammography only in a 38-year-old woman. The other 7 mammography-only breast cancers were diagnosed in women aged 50 years and older, increasing sensitivity in this subgroup from 79.5% (35/44) to 95.5% (42/44) (p ≤ 0.001). In BRCA2 mutation carriers younger than 40 years, the benefit of mammographic screening over MRI was very small. In carriers of 50 years and older, mammographic screening contributed significantly. Hence, we propose to postpone mammographic screening in BRCA2 mutation carriers to at least age 40.

Identifiants

pubmed: 32333294
doi: 10.1007/s10549-020-05642-1
pii: 10.1007/s10549-020-05642-1
pmc: PMC7220868
doi:

Substances chimiques

BRCA2 Protein 0
BRCA2 protein, human 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

581-588

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Auteurs

Inge-Marie Obdeijn (IM)

Department of Radiology and Nuclear Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands. a.obdeijn@erasmusmc.nl.

Ritse M Mann (RM)

Department of Radiology and Nuclear Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Radiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Claudette C E Loo (CCE)

Department of Radiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Marc Lobbes (M)

Department of Medical Imaging, Zuyderland Medical Center, Sittard-Geleen, The Netherlands.
Department of Radiology and Nuclear Medicine, University Medical Center, Maastricht, The Netherlands.
GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, The Netherlands.

Eleonora M C Voormolen (EMC)

Department of Radiology and Nuclear Medicine, Leiden University Medical Center, Leiden, The Netherlands.

Carolien H M van Deurzen (CHM)

Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Geertruida de Bock (G)

Department of Epidemiology, University Medical Center, Groningen, The Netherlands.

Maartje J Hooning (MJ)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

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