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dc.date.accessioned2020-07-08T19:30:34Z
dc.date.available2020-07-08T19:30:34Z
dc.date.created2016-07-15T09:59:36Z
dc.date.issued2016
dc.identifier.citationEvans, Dafydd Gareth Harkness, Elaine F. Howell, Anthony Wilson, Mary Hurley, Emma Holmen, Marit Muri Tharmaratnam, Kukatharmini Hagen, Anne Irene Lim, Yit Yoong Maxwell, Anthony James Møller, Pål . Intensive breast screening in BRCA2 mutation carriers is associated with reduced breast cancer specific and all cause mortality. Hereditary Cancer in Clinical Practice. 2016, 14(8)
dc.identifier.urihttp://hdl.handle.net/10852/77669
dc.description.abstractBackground The addition of annual MRI screening to mammography has heightened optimism that intensive screening along with improved treatments may substantially improve life expectancy of women at high risk of breast cancer. However, survival data from BRCA2 mutation carriers undergoing intensive combined breast screening are scarce. Methods We have collated the results of screening with either annual mammography or mammography with MRI in female BRCA2 mutation carriers in Manchester and Oslo and use a Manchester control group of BRCA2 mutation carriers who had their first breast cancer diagnosed without intensive screening. Results Eighty-seven BRCA2 mutation carriers had undergone combined (n = 34) or mammography (n = 53) screening compared to 274 without such intensive screening. Ten year breast cancer specific survival was 100 % in the combined group (95 % CI 82.5–100 %) and 85.5 % (95 % CI 72.6–98.4 %) in the mammography group compared to 74.6 % (95 % CI 66.6–82.6 %) in the control group. Better survival was driven by lymph node status (negative in 67 % of screened vs 39 % of unscreened women; p < 0.001) and a significantly greater proportion of intensively screened women had invasive breast cancers <2 cm at diagnosis (74.6 % vs 50.4 %; p = 0.002). Conclusion Intensive combined breast cancer screening with annual MRI and mammography appears to improve survival from breast cancer in BRCA2 mutation carriers. Data from larger groups are required to confirm the effectiveness of combined screening in BRCA2 carriers.
dc.languageEN
dc.publisherBioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleIntensive breast screening in BRCA2 mutation carriers is associated with reduced breast cancer specific and all cause mortality
dc.typeJournal article
dc.creator.authorEvans, Dafydd Gareth
dc.creator.authorHarkness, Elaine F.
dc.creator.authorHowell, Anthony
dc.creator.authorWilson, Mary
dc.creator.authorHurley, Emma
dc.creator.authorHolmen, Marit Muri
dc.creator.authorTharmaratnam, Kukatharmini
dc.creator.authorHagen, Anne Irene
dc.creator.authorLim, Yit Yoong
dc.creator.authorMaxwell, Anthony James
dc.creator.authorMøller, Pål
cristin.unitcode185,15,13,0
cristin.unitnameMatematisk institutt
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1368121
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Hereditary Cancer in Clinical Practice&rft.volume=14&rft.spage=&rft.date=2016
dc.identifier.jtitleHereditary Cancer in Clinical Practice
dc.identifier.volume14
dc.identifier.issue1
dc.identifier.doihttps://doi.org/10.1186/s13053-016-0048-3
dc.identifier.urnURN:NBN:no-80735
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1731-2302
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/77669/2/Evans.pdf
dc.type.versionPublishedVersion
cristin.articleid8


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