Evidence map›Paper›PMID 39161644›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering2022

Spatial dependency of lesion detectability in digital breast tomosynthesis.

Chloe J Choi, Bruno Barufaldi, João P V Teixeira, Raymond J Acciavatti, Andrew D A Maidment

Abstract read
In one paragraph

Article in Proceedings of SPIE--the International Society for Optical Engineering, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Chloe J ChoiDepartment of Radiology, University of Pennsylvania, Philadelphia, USA.
Bruno BarufaldiDepartment of Radiology, University of Pennsylvania, Philadelphia, USA.
João P V TeixeiraFederal University of Paraiba, João Pessoa, Brazil.
Raymond J AcciavattiDepartment of Radiology, University of Pennsylvania, Philadelphia, USA.
Andrew D A MaidmentDepartment of Radiology, University of Pennsylvania, Philadelphia, USA.

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
High Performance, Quantitative Breast PET Scanner Integrated With TomosynthesisR01CA196528 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ANDREW DOUGLAS ARNOLD MAIDMENT, Suleman Surti · 2016 to 2026
$5.9M
Training Program in Biomedical Imaging and Information SciencesT32EB009384 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI GEE, JAMES C, IVES, ZACHARY · 2009 to 2023
$4.0M
NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA196528NIBIB NIH HHS T32 EB009384
6 · The paper itself

Abstract

X-ray imaging results in inhomogeneous irradiation of the detector and distortion of structures in the periphery of the image; yet the spatial dependency of tomosynthesis image-quality metrics has not been extensively investigated. In this study, we use virtual clinical trials to quantify the spatial dependency of lesion detectability in our lab's next-generation tomosynthesis (NGT) system. Two geometries were analyzed: a conventional geometry with mediolateral source motion, and a NGT geometry with T-shaped motion. Breast parenchymal texture was simulated using an open-source library with Perlin noise using 400 random seeds and three breast densities. Spherical mass lesions were inserted in the central slice of the phantoms using the voxel additive method. Image acquisition was simulated using in-house ray-tracing software and simple backprojection was performed using commercial reconstruction software. Lesion detectability with Channelized Hotelling Observers (CHOs) was analyzed using receiver operating characteristic curves to measure the detectability index (d') at 154 unique locations for the lesions. We also divided images into three non-overlapping regions (differing in terms of distance from the chest wall). At the 0.05 level of significance, there was a statistically significant difference between the geometries in terms of d' in one of the three regions, with the T geometry offering superior detectability. Examining all 154 lesion locations, the T geometry was found to offer lower spread (standard deviation) in d' values throughout the image area, and superior d' at 83 of 154 locations (53.9%). In summary, the T geometry enables superior lesion detection and mitigates anisotropies.

Indexed as

Breast CancerDigital Breast Tomosynthesis (DBT)Image QualitySensitivitySpecificityVirtual Clinical Trial (VCT)

Identifiers

PMID39161644
PMCPMC11333122

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.