Interactive Transcript
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In terms of performance, we certainly know that by looking through
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many tomosome slices, this increases our reading time compared to standard
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2D demography, has a significant impact on operational workflows and
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staffing. Multiple studies have demonstrated a reduction in recall rate
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and increase in cancer detection rate for DBT compared to 2D alone. Screening
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performance improvements are likely related to DBT ability to detect cancers
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even when obscured by dense tissue and also differentiate true lesions from
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tissue overlap. Best estimates of reducing recall rate is about 15%
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and may increase our cancer detection rate or CDR by about 30%
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and this is true even in patients with
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lower breast density, suggesting that DBT improves cancer conspicuity. Of
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course, people have started to use DBT in the diagnostic setting as well,
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not just screening. And research has shown that this improves abnormal interpretation
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rate, meaning that it decreases that. Increases PPV, both PPV2 and PPV3,
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with a higher proportion of invasive cancers identified. DBT can replace
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standard 2D diagnostic use for non calcified lesions. So your standard mass
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or asymmetry with improved diagnostic accuracy. It also offers the potential
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benefit of more efficient imaging with fewer views, potentially even without
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additional diagnostic mammography and proceeding directly to ultrasound.
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This last point is still, I'd say, talked about a little bit in
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the literature about what is the best method and practices will make up
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their own individual decision about how they feel about this. There are
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some people that argue that screening DBT provides the same
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amount of lesion localization, margin detection as doing additional views
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and therefore the additional diagnostic mammogram views are not necessary
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and you could go directly to ultrasound. There are other practices that
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feel that doing those additional DBT views in the diagnostic setting do
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still improve your ability to describe lesions and identify lesions.
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And also prefer that for an operational reason,
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meaning that it's easier to go ahead and do your mammogram first and
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then ultrasound and you get the benefit of doing additional sort of non
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standard views such as a medial lateral view or maybe an XCCL tomo view
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or something like that to better help you identify or localize that lesion.
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In terms of pathology outcomes, there's increased identification of architectural
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distortion with DBT and these architectural distortions tend to be less
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likely to be malignant compared to 2D, meaning that we probably see more
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radial scars and complex sclerosing lesions, which depending on your practice,
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either be considered benign or high risk, but it also improves diagnosis
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of invasive breast cancers, which tend to be smaller,
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lower grade in earlier stage and no negative. And we also see more
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invasive lobular carcinomas largely due to the fact that they're probably
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just more conspicuous on DBT as those are one of the most difficult
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invasive cancers to identify on mammography.
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