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dc.contributor.authorHoussami, Nehmat
dc.contributor.authorSolveig, Hofvind
dc.contributor.authorSoerensen, Anne L
dc.contributor.authorRobledo, Kristy P
dc.contributor.authorHunter, Kylie
dc.contributor.authorBernardi, Daniela
dc.contributor.authorLang, Kristina
dc.contributor.authorJohnson, Kristin
dc.contributor.authorAglen, Camilla
dc.contributor.authorZackrisson, Sophia
dc.date.accessioned2021-07-14T05:15:53Z
dc.date.available2021-07-14T05:15:53Z
dc.date.issued2021en_AU
dc.identifier.urihttps://hdl.handle.net/2123/25686
dc.description.abstractBackground: Digital breast tomosynthesis (DBT) improves breast cancer (BC) detection compared to mammography, however, it is unknown whether this reduces interval cancer rate (ICR) at follow-up. Methods: Using individual participant data (IPD) from DBT screening studies (identified via periodic literature searches July 2016 to November 2019) we performed an IPD meta-analysis. We estimated ICR for DBT-screened participants and the difference in pooled ICR for DBT and mammography-only screening, and compared interval BC characteristics. Two-stage meta-analysis (study-specific estimation, pooled synthesis) of ICR included random-effects, adjusting for study and age, and was estimated in age and density subgroups. Comparative screening sensitivity was calculated using screen-detected and interval BC data. Findings: Four prospective DBT studies, from European population-based programs, contributed IPD for 66,451 DBT-screened participants: age-adjusted pooled ICR was 13.17/10,000 (95%CI: 8.25-21.02). Pooled ICR was higher in the high-density (21.08/10,000; 95%CI: 6.71-66.27) than the low-density (8.63/10,000; 95%CI: 5.25-14.192) groups (P = 0.03) however estimates did not differ across age-groups (P = 0.32). Based on two studies that also provided data for 153,800 mammography screens (age-adjusted ICR 17.69/10,000; 95%CI: 13.22-23.66), DBT's pooled ICR was 16.83/10,000 (95%CI: 11.89-23.82). Comparative meta-analysis showed a non-significant difference in ICR (-0.44/10,000; 95%CI: -11.00-10.11) and non-significant difference in screening sensitivity (6.79%; 95%CI: -0.73-14.87%) between DBT and DM but a significant pooled difference in cancer detection rate of 33.49/10,000 (95%CI: 23.88-43.10). Distribution of interval BC prognostic characteristics did not differ between screening modalities except that those occurring in DBT-screened participants were significantly more likely to be negative for axillary-node metastases (P = 0.005). Interpretation: Although heterogeneity in ICR estimates and few datasets limit recommendations, there was no difference between DBT and mammography in pooled ICR despite DBT increasing cancer detection. (C) 2021 The Author(s). Published by Elsevier Ltd.en_AU
dc.language.isoenen_AU
dc.publisherElsevieren_AU
dc.relation.ispartofEClinicalMedicineen_AU
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en_AU
dc.subjectbreast canceren_AU
dc.subjectcancer screeningen_AU
dc.subjectdigital breast tomosynthesisen_AU
dc.subjectinterval canceren_AU
dc.subjectmammographyen_AU
dc.subjectmeta-analysisen_AU
dc.titleInterval breast cancer rates for digital breast tomosynthesis versus digital mammography population screening: An individual participant data meta-analysisen_AU
dc.typeArticleen_AU
dc.subject.asrc11 Medical and Health Sciencesen_AU
dc.identifier.doi10.1016/j.eclinm.2021.100804
dc.relation.otherNational Breast Cancer Foundation
dc.relation.otherBreast Cancer Research Leadership Fellowship (Awarded to NH)
usyd.facultyFaculty of Medicine and Health, Sydney School of Public Healthen_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::NHMRC Clinical Trials Centreen_AU
usyd.citation.volume34en_AU
workflow.metadata.onlyNoen_AU


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