Dedicated Photon-Counting CT for Detection and Classification of Microcalcifications: An Intraindividual Comparison With Digital Breast Tomosynthesis.

IF 7 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Investigative Radiology Pub Date : 2024-12-01 Epub Date: 2024-06-27 DOI:10.1097/RLI.0000000000001097
Luisa Charlotte Huck, Maike Bode, Eloisa Zanderigo, Caroline Wilpert, Vanessa Raaff, Ebba Dethlefsen, Evelyn Wenkel, Christiane Katharina Kuhl
{"title":"Dedicated Photon-Counting CT for Detection and Classification of Microcalcifications: An Intraindividual Comparison With Digital Breast Tomosynthesis.","authors":"Luisa Charlotte Huck, Maike Bode, Eloisa Zanderigo, Caroline Wilpert, Vanessa Raaff, Ebba Dethlefsen, Evelyn Wenkel, Christiane Katharina Kuhl","doi":"10.1097/RLI.0000000000001097","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Clinical experience regarding the use of dedicated photon-counting breast CT (PC-BCT) for diagnosis of breast microcalcifications is scarce. This study systematically compares the detection and classification of breast microcalcifications using a dedicated breast photon-counting CT, especially designed for examining the breast, in comparison with digital breast tomosynthesis (DBT).</p><p><strong>Materials and methods: </strong>This is a prospective intraindividual study on women with DBT screening-detected BI-RADS-4/-5 microcalcifications who underwent PC-BCT before biopsy. PC-BCT images were reconstructed with a noninterpolated spatial resolution of 0.15 × 0.15 × 0.15 mm (reconstruction mode 1 [RM-1]) and with 0.3 × 0.3 × 0.3 mm (reconstruction mode 2 [RM-2]), plus thin-slab maximum intensity projection (MIP) reconstructions. Two radiologists independently rated the detection of microcalcifications in direct comparison with DBT on a 5-point scale. The distribution and morphology of microcalcifications were then rated according to BI-RADS. The size of the smallest discernible microcalcification particle was measured. For PC-BCT, the average glandular dose was determined by Monte Carlo simulations; for DBT, the information provided by the DBT system was used.</p><p><strong>Results: </strong>Between September 2022 and July 2023, 22 participants (mean age, 61; range, 42-85 years) with microcalcifications (16 malignant; 6 benign) were included. In 2/22 with microcalcifications in the posterior region, microcalcifications were not detectable on PC-BCT, likely because they were not included in the PC-BCT volume. In the remaining 20 participants, microcalcifications were detectable. With high between-reader agreement (κ > 0.8), conspicuity of microcalcifications was rated similar for DBT and MIPs of RM-1 (mean, 4.83 ± 0.38 vs 4.86 ± 0.35) ( P = 0.66), but was significantly lower ( P < 0.05) for the remaining PC-BCT reconstructions: 2.11 ± 0.92 (RM-2), 2.64 ± 0.80 (MIPs of RM-2), and 3.50 ± 1.23 (RM-1). Identical distribution qualifiers were assigned for PC-BCT and DBT in 18/20 participants, with excellent agreement (κ = 0.91), whereas identical morphologic qualifiers were assigned in only 5/20, with poor agreement (κ = 0.44). The median size of smallest discernible microcalcification particle was 0.2 versus 0.6 versus 1.1 mm in DBT versus RM-1 versus RM-2 ( P < 0.001), likely due to blooming effects. Average glandular dose was 7.04 mGy (PC-BCT) versus 6.88 mGy (DBT) ( P = 0.67).</p><p><strong>Conclusions: </strong>PC-BCT allows reliable detection of in-breast microcalcifications as long as they are not located in the posterior part of the breast and allows assessment of their distribution, but not of their individual morphology.</p>","PeriodicalId":14486,"journal":{"name":"Investigative Radiology","volume":" ","pages":"838-844"},"PeriodicalIF":7.0000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Investigative Radiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/RLI.0000000000001097","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Clinical experience regarding the use of dedicated photon-counting breast CT (PC-BCT) for diagnosis of breast microcalcifications is scarce. This study systematically compares the detection and classification of breast microcalcifications using a dedicated breast photon-counting CT, especially designed for examining the breast, in comparison with digital breast tomosynthesis (DBT).

Materials and methods: This is a prospective intraindividual study on women with DBT screening-detected BI-RADS-4/-5 microcalcifications who underwent PC-BCT before biopsy. PC-BCT images were reconstructed with a noninterpolated spatial resolution of 0.15 × 0.15 × 0.15 mm (reconstruction mode 1 [RM-1]) and with 0.3 × 0.3 × 0.3 mm (reconstruction mode 2 [RM-2]), plus thin-slab maximum intensity projection (MIP) reconstructions. Two radiologists independently rated the detection of microcalcifications in direct comparison with DBT on a 5-point scale. The distribution and morphology of microcalcifications were then rated according to BI-RADS. The size of the smallest discernible microcalcification particle was measured. For PC-BCT, the average glandular dose was determined by Monte Carlo simulations; for DBT, the information provided by the DBT system was used.

Results: Between September 2022 and July 2023, 22 participants (mean age, 61; range, 42-85 years) with microcalcifications (16 malignant; 6 benign) were included. In 2/22 with microcalcifications in the posterior region, microcalcifications were not detectable on PC-BCT, likely because they were not included in the PC-BCT volume. In the remaining 20 participants, microcalcifications were detectable. With high between-reader agreement (κ > 0.8), conspicuity of microcalcifications was rated similar for DBT and MIPs of RM-1 (mean, 4.83 ± 0.38 vs 4.86 ± 0.35) ( P = 0.66), but was significantly lower ( P < 0.05) for the remaining PC-BCT reconstructions: 2.11 ± 0.92 (RM-2), 2.64 ± 0.80 (MIPs of RM-2), and 3.50 ± 1.23 (RM-1). Identical distribution qualifiers were assigned for PC-BCT and DBT in 18/20 participants, with excellent agreement (κ = 0.91), whereas identical morphologic qualifiers were assigned in only 5/20, with poor agreement (κ = 0.44). The median size of smallest discernible microcalcification particle was 0.2 versus 0.6 versus 1.1 mm in DBT versus RM-1 versus RM-2 ( P < 0.001), likely due to blooming effects. Average glandular dose was 7.04 mGy (PC-BCT) versus 6.88 mGy (DBT) ( P = 0.67).

Conclusions: PC-BCT allows reliable detection of in-breast microcalcifications as long as they are not located in the posterior part of the breast and allows assessment of their distribution, but not of their individual morphology.

用于微钙化检测和分类的专用光子计数 CT:与数字乳腺断层扫描的个体内比较。
目的:使用专用光子计数乳腺 CT(PC-BCT)诊断乳腺微钙化的临床经验很少。本研究系统地比较了使用专门用于检查乳腺的专用乳腺光子计数 CT 与数字乳腺断层扫描(DBT)对乳腺微小钙化的检测和分类:这是一项前瞻性个体内研究,研究对象是 DBT 筛查发现 BI-RADS-4/-5 微钙化并在活检前接受 PC-BCT 检查的女性。PC-BCT图像的非插值空间分辨率为0.15 × 0.15 × 0.15 mm(重建模式1 [RM-1])和0.3 × 0.3 × 0.3 mm(重建模式2 [RM-2]),加上薄板最大强度投影(MIP)重建。与 DBT 直接比较微钙化的检出率,由两名放射科医生以 5 分制独立评分。然后根据 BI-RADS 对微钙化的分布和形态进行评分。测量可辨认的最小微钙化颗粒的大小。对于 PC-BCT,平均腺体剂量通过蒙特卡洛模拟确定;对于 DBT,则使用 DBT 系统提供的信息:结果:2022 年 9 月至 2023 年 7 月间,22 名参与者(平均年龄 61 岁;年龄范围 42-85 岁)患有微钙化(16 例恶性;6 例良性)。在 2/22 名后部微钙化患者中,PC-BCT 无法检测到微钙化,这可能是因为微钙化未包括在 PC-BCT 容量中。其余 20 名参与者均可检测到微钙化。阅片者之间的一致性很高(κ > 0.8),DBT 和 RM-1 的 MIP(平均值为 4.83 ± 0.38 vs 4.86 ± 0.35)(P = 0.66)对微钙化的明显性评价相似,但其余 PC-BCT 重建的微钙化明显较低(P < 0.05):2.11 ± 0.92(RM-2)、2.64 ± 0.80(RM-2 的 MIPs)和 3.50 ± 1.23(RM-1)。在 18/20 名参与者中,PC-BCT 和 DBT 分配了相同的分布限定词,一致性极佳(κ = 0.91),而只有 5/20 名参与者分配了相同的形态限定词,一致性较差(κ = 0.44)。DBT与RM-1和RM-2相比,可辨认的最小微钙化颗粒的中位尺寸分别为0.2和0.6和1.1毫米(P < 0.001),这可能是由于开花效应造成的。平均腺体剂量为 7.04 mGy(PC-BCT)对 6.88 mGy(DBT)(P = 0.67):PC-BCT能可靠地检测出乳房内的微钙化,只要它们不位于乳房后部,并能评估它们的分布,但不能评估它们的个体形态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Investigative Radiology
Investigative Radiology 医学-核医学
CiteScore
15.10
自引率
16.40%
发文量
188
审稿时长
4-8 weeks
期刊介绍: Investigative Radiology publishes original, peer-reviewed reports on clinical and laboratory investigations in diagnostic imaging, the diagnostic use of radioactive isotopes, computed tomography, positron emission tomography, magnetic resonance imaging, ultrasound, digital subtraction angiography, and related modalities. Emphasis is on early and timely publication. Primarily research-oriented, the journal also includes a wide variety of features of interest to clinical radiologists.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信