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ECR 2024 Book of Abstracts ECR 2024 摘要集
IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-18 DOI: 10.1186/s13244-024-01766-w
<p><b>Open Access</b> This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.</p><p>Reprints and permissions</p><img alt="Check for updates. Verify currency and authenticity via CrossMark" height="81" loading="lazy" src="data:image/svg+xml;base64,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
开放存取 本文采用知识共享署名 4.0 国际许可协议进行许可,该协议允许以任何媒介或格式使用、共享、改编、分发和复制本文,但需适当注明原作者和出处,提供知识共享许可协议的链接,并说明是否进行了修改。本文中的图片或其他第三方材料均包含在文章的知识共享许可协议中,除非在材料的署名栏中另有说明。如果材料未包含在文章的知识共享许可协议中,且您打算使用的材料不符合法律规定或超出许可使用范围,您需要直接从版权所有者处获得许可。要查看该许可的副本,请访问 http://creativecommons.org/licenses/by/4.0/.Reprints and permissionsCite this article ECR 2024 Book of Abstracts.Insights Imaging 15 (Suppl 2), 223 (2024). https://doi.org/10.1186/s13244-024-01766-wDownload citationPublished: 18 September 2024DOI: https://doi.org/10.1186/s13244-024-01766-wShare this articleAnyone you share the following link with will be able to read this content:Get shareable linkSorry, a shareable link is not currently available for this article.Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative
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引用次数: 0
Focal cortical dysplasia lesion segmentation using multiscale transformer 使用多尺度变换器分割局灶性皮质发育不良病灶
IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-12 DOI: 10.1186/s13244-024-01803-8
Xiaodong Zhang, Yongquan Zhang, Changmiao Wang, Lin Li, Fengjun Zhu, Yang Sun, Tong Mo, Qingmao Hu, Jinping Xu, Dezhi Cao
Accurate segmentation of focal cortical dysplasia (FCD) lesions from MR images plays an important role in surgical planning and decision but is still challenging for radiologists and clinicians. In this study, we introduce a novel transformer-based model, designed for the end-to-end segmentation of FCD lesions from multi-channel MR images. The core innovation of our proposed model is the integration of a convolutional neural network-based encoder-decoder structure with a multiscale transformer to augment the feature representation of lesions in the global field of view. Transformer pathways, composed of memory- and computation-efficient dual-self-attention modules, leverage feature maps from varying depths of the encoder to discern long-range interdependencies among feature positions and channels, thereby emphasizing areas and channels relevant to lesions. The proposed model was trained and evaluated on a public-open dataset including MR images of 85 patients using both subject-level and voxel-level metrics. Experimental results indicate that our model offers superior performance both quantitatively and qualitatively. It successfully identified lesions in 82.4% of patients, with a low false-positive lesion cluster rate of 0.176 ± 0.381 per patient. Furthermore, the model achieved an average Dice coefficient of 0.410 ± 0.288, outperforming five established methods. Integration of the transformer could enhance the feature presentation and segmentation performance of FCD lesions. The proposed model has the potential to serve as a valuable assistive tool for physicians, enabling rapid and accurate identification of FCD lesions. The source code and pre-trained model weights are available at https://github.com/zhangxd0530/MS-DSA-NET . This multiscale transformer-based model performs segmentation of focal cortical dysplasia lesions, aiming to help radiologists and clinicians make accurate and efficient preoperative evaluations of focal cortical dysplasia patients from MR images.
从磁共振图像中准确分割局灶性皮质发育不良(FCD)病变在手术规划和决策中起着重要作用,但对放射科医生和临床医生来说仍具有挑战性。在本研究中,我们介绍了一种基于变压器的新型模型,该模型专为从多通道磁共振图像中对 FCD 病灶进行端到端分割而设计。我们提出的模型的核心创新点是将基于卷积神经网络的编码器-解码器结构与多尺度变换器相结合,以增强病变在全局视野中的特征表示。转换器通路由记忆和计算效率高的双自我注意模块组成,利用来自不同深度编码器的特征图来辨别特征位置和通道之间的长程相互依存关系,从而强调与病变相关的区域和通道。我们在一个公开数据集上使用主体级和体素级指标对所提出的模型进行了训练和评估,该数据集包括 85 名患者的磁共振图像。实验结果表明,我们的模型在定量和定性方面都表现出色。它成功识别了 82.4% 患者的病灶,每位患者的病灶群假阳性率低至 0.176 ± 0.381。此外,该模型的平均 Dice 系数为 0.410 ± 0.288,优于五种既有方法。转换器的集成可以提高 FCD 病变的特征呈现和分割性能。所提出的模型有望成为医生的重要辅助工具,从而快速准确地识别 FCD 病变。源代码和预训练模型权重可在 https://github.com/zhangxd0530/MS-DSA-NET 上获取。这个基于多尺度变换器的模型可对局灶性皮质发育不良病变进行分割,旨在帮助放射科医生和临床医生从磁共振图像中对局灶性皮质发育不良患者进行准确有效的术前评估。
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引用次数: 0
ESHNR 2024 Book of Abstracts ESHNR 2024 摘要集
IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-12 DOI: 10.1186/s13244-024-01789-3
<p><b>Open Access</b> This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.</p><p>Reprints and permissions</p><img alt="Check for updates. Verify currency and authenticity via CrossMark" height="81" loading="lazy" src="data:image/svg+xml;base64,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
开放存取 本文采用知识共享署名 4.0 国际许可协议进行许可,该协议允许以任何媒介或格式使用、共享、改编、分发和复制本文,但需适当注明原作者和出处,提供知识共享许可协议的链接,并说明是否进行了修改。本文中的图片或其他第三方材料均包含在文章的知识共享许可协议中,除非在材料的署名栏中另有说明。如果材料未包含在文章的知识共享许可协议中,且您打算使用的材料不符合法律规定或超出许可使用范围,您需要直接从版权所有者处获得许可。要查看该许可的副本,请访问 http://creativecommons.org/licenses/by/4.0/.Reprints and permissionsCite this article ESHNR 2024 Book of Abstracts.Insights Imaging 15 (Suppl 3), 221 (2024). https://doi.org/10.1186/s13244-024-01789-3Download citationPublished: 12 September 2024DOI: https://doi.org/10.1186/s13244-024-01789-3Share this articleAnyone you share the following link with will be able to read this content:Get shareable linkSorry, a shareable link is not currently available for this article.Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative
{"title":"ESHNR 2024 Book of Abstracts","authors":"","doi":"10.1186/s13244-024-01789-3","DOIUrl":"https://doi.org/10.1186/s13244-024-01789-3","url":null,"abstract":"&lt;p&gt;&lt;b&gt;Open Access&lt;/b&gt; This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.&lt;/p&gt;\u0000&lt;p&gt;Reprints and permissions&lt;/p&gt;&lt;img alt=\"Check for updates. Verify currency and authenticity via CrossMark\" height=\"81\" loading=\"lazy\" src=\"data:image/svg+xml;base64,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","PeriodicalId":13639,"journal":{"name":"Insights into Imaging","volume":"30 1","pages":""},"PeriodicalIF":4.7,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142259344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of proliferative hepatocellular carcinoma using the SMARS score and implications for microwave ablation 使用 SMARS 评分识别增生性肝细胞癌及其对微波消融的影响
IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-09-10 DOI: 10.1186/s13244-024-01792-8
Peng Zhou, Yan Bao, De-Hua Chang, Jun-Xiang Li, Tian-Zhi An, Ya-Ping Shen, Wen-Wu Cai, Lu Wen, Yu-Dong Xiao
To compare therapeutic outcomes of predicted proliferative and nonproliferative hepatocellular carcinoma (HCC) after microwave ablation (MWA) using a previously developed imaging-based predictive model, the SMARS score. This multicenter retrospective study included consecutive 635 patients with unresectable HCC who underwent MWA between August 2013 and September 2020. Patients were stratified into predicted proliferative and nonproliferative phenotypes according to the SMARS score. Overall survival (OS) and recurrence-free survival (RFS) were compared between the predicted proliferative and nonproliferative HCCs before and after propensity score matching (PSM). OS and RFS were also compared between the two groups in subgroups of tumor size smaller than 30 mm and tumor size 30–50 mm. The SMARS score classified 127 and 508 patients into predicted proliferative and nonproliferative HCCs, respectively. The predicted proliferative HCCs exhibited worse RFS but equivalent OS when compared with nonproliferative HCCs before (p < 0.001 for RFS; p = 0.166 for OS) and after (p < 0.001 for RFS; p = 0.456 for OS) matching. Regarding subgroups of tumor size smaller than 30 mm (p = 0.098) and tumor size 30–50 mm (p = 0.680), the OSs were similar between the two groups. However, predicted proliferative HCCs had worse RFS compared to nonproliferative HCCs in the subgroup of tumor size 30–50 mm (p < 0.001), while the RFS did not differ in the subgroup of tumor size smaller than 30 mm (p = 0.141). Predicted proliferative HCCs have worse RFS than nonproliferative ones after MWA, especially in tumor size larger than 30 mm. However, the phenotype of the tumor may not affect the OS. Before performing microwave ablation for hepatocellular carcinoma, the tumor phenotype should be considered because it may affect the therapeutic outcome.
利用之前开发的基于成像的预测模型--SMARS评分,比较微波消融(MWA)术后预测增生性和非增生性肝细胞癌(HCC)的治疗效果。这项多中心回顾性研究纳入了 2013 年 8 月至 2020 年 9 月期间接受微波消融术的 635 例不可切除 HCC 患者。根据SMARS评分,患者被分为预测增殖和非增殖表型。比较了倾向评分匹配(PSM)前后预测增殖型和非增殖型HCC的总生存期(OS)和无复发生存期(RFS)。此外,还比较了肿瘤大小小于 30 毫米和肿瘤大小 30-50 毫米亚组两组患者的 OS 和 RFS。SMARS评分将127名和508名患者分别分为预测增殖性和非增殖性HCC。与匹配前(RFS p < 0.001;OS p = 0.166)和匹配后(RFS p < 0.001;OS p = 0.456)的非增殖性HCC相比,预测增殖性HCC的RFS较差,但OS相当。在肿瘤大小小于30毫米(p = 0.098)和肿瘤大小为30-50毫米(p = 0.680)的亚组中,两组的OS相似。然而,在肿瘤大小为 30-50 mm 的亚组中,预测增殖性 HCC 的 RFS 比非增殖性 HCC 更差(p < 0.001),而在肿瘤大小小于 30 mm 的亚组中,RFS 没有差异(p = 0.141)。预测增殖性 HCC 在 MWA 后的 RFS 比非增殖性 HCC 差,尤其是肿瘤大小大于 30 毫米的 HCC。不过,肿瘤的表型可能不会影响OS。在对肝细胞癌进行微波消融之前,应考虑肿瘤的表型,因为它可能会影响治疗效果。
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引用次数: 0
Critical but commonly neglected factors that affect contrast medium administration in CT. 影响 CT 造影剂使用的关键但通常被忽视的因素。
IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-08-28 DOI: 10.1186/s13244-024-01750-4
Michael C McDermott, Joachim E Wildberger, Kyongtae T Bae

Objective: Past decades of research into contrast media injections and optimization thereof in radiology clinics have focused on scan acquisition parameters, patient-related factors, and contrast injection protocol variables. In this review, evidence is provided that a fourth bucket of crucial variables has been missed which account for previously unexplained phenomena and higher-than-expected variability in data. We propose how these critical factors should be considered and implemented in the contrast-medium administration protocols to optimize contrast enhancement.

Methods: This article leverages a combination of methodologies for uncovering and quantifying confounding variables associated with or affecting the contrast-medium injection. Engineering benchtop equipment such as Coriolis flow meters, pressure transducers, and volumetric measurement devices are combined with small, targeted systematic evaluations querying operators, equipment, and the physics and fluid dynamics that make a seemingly simple task of injecting fluid into a patient a complex and non-linear endeavor.

Results: Evidence is presented around seven key factors affecting the contrast-medium injection including a new way of selecting optimal IV catheters, degraded performance from longer tubing sets, variability associated with the mechanical injection system technology, common operator errors, fluids exchanging places stealthily based on gravity and density, wasted contrast media and inefficient saline flushes, as well as variability in the injected flow rate vs. theoretical expectations.

Conclusion: There remain several critical, but not commonly known, sources of error associated with contrast-medium injections. Elimination of these hidden sources of error where possible can bring immediate benefits and help to drive standardized and optimized contrast-media injections.

Critical relevance statement: This review brings to light the commonly neglected/unknown factors negatively impacting contrast-medium injections and provides recommendations that can result in patient benefits, quality improvements, sustainability increases, and financial benefits by enabling otherwise unachievable optimization.

Key points: How IV contrast media is administered is a rarely considered source of CT imaging variability. IV catheter selection, tubing length, injection systems, and insufficient flushing can result in unintended variability. These findings can be immediately addressed to improve standardization in contrast-enhanced CT imaging.

目的:过去几十年来,放射科诊所对造影剂注射及其优化的研究主要集中在扫描采集参数、患者相关因素和造影剂注射方案变量上。在这篇综述中,我们提供的证据表明,人们忽略了第四类关键变量,而这些变量正是以前无法解释的现象和数据变异性高于预期的原因。我们建议在造影剂给药方案中应如何考虑和实施这些关键因素,以优化造影剂的增强效果:本文利用多种方法来揭示和量化与造影剂注射相关或影响造影剂注射的混杂变量。科里奥利流量计、压力传感器和容积测量装置等工程台式设备与小规模、有针对性的系统评估相结合,对操作人员、设备以及物理和流体动力学进行询问,这些因素使得向患者注射液体这一看似简单的任务变得复杂而非线性:结果:围绕影响造影剂注射的七个关键因素提供了证据,包括选择最佳静脉导管的新方法、较长管道组导致的性能下降、与机械注射系统技术相关的可变性、常见的操作错误、基于重力和密度的液体隐蔽交换位置、造影剂浪费和低效的生理盐水冲洗,以及注射流速与理论期望值之间的可变性:结论:造影剂注射仍存在几个关键但不为人知的误差源。尽可能消除这些隐藏的误差源可带来立竿见影的效果,并有助于推动造影剂注射的标准化和优化:这篇综述揭示了通常被忽视/不为人知的对造影剂注射产生负面影响的因素,并提出了一些建议,通过实现原本无法实现的优化,可为患者带来益处、质量改善、可持续性提高和经济效益:要点:静脉注射造影剂的方式是造成 CT 成像变化的一个很少被考虑的因素。静脉注射导管的选择、管道长度、注射系统和冲洗不足都可能导致意外的变异。这些发现可以立即得到解决,以提高造影剂增强 CT 成像的标准化程度。
{"title":"Critical but commonly neglected factors that affect contrast medium administration in CT.","authors":"Michael C McDermott, Joachim E Wildberger, Kyongtae T Bae","doi":"10.1186/s13244-024-01750-4","DOIUrl":"10.1186/s13244-024-01750-4","url":null,"abstract":"<p><strong>Objective: </strong>Past decades of research into contrast media injections and optimization thereof in radiology clinics have focused on scan acquisition parameters, patient-related factors, and contrast injection protocol variables. In this review, evidence is provided that a fourth bucket of crucial variables has been missed which account for previously unexplained phenomena and higher-than-expected variability in data. We propose how these critical factors should be considered and implemented in the contrast-medium administration protocols to optimize contrast enhancement.</p><p><strong>Methods: </strong>This article leverages a combination of methodologies for uncovering and quantifying confounding variables associated with or affecting the contrast-medium injection. Engineering benchtop equipment such as Coriolis flow meters, pressure transducers, and volumetric measurement devices are combined with small, targeted systematic evaluations querying operators, equipment, and the physics and fluid dynamics that make a seemingly simple task of injecting fluid into a patient a complex and non-linear endeavor.</p><p><strong>Results: </strong>Evidence is presented around seven key factors affecting the contrast-medium injection including a new way of selecting optimal IV catheters, degraded performance from longer tubing sets, variability associated with the mechanical injection system technology, common operator errors, fluids exchanging places stealthily based on gravity and density, wasted contrast media and inefficient saline flushes, as well as variability in the injected flow rate vs. theoretical expectations.</p><p><strong>Conclusion: </strong>There remain several critical, but not commonly known, sources of error associated with contrast-medium injections. Elimination of these hidden sources of error where possible can bring immediate benefits and help to drive standardized and optimized contrast-media injections.</p><p><strong>Critical relevance statement: </strong>This review brings to light the commonly neglected/unknown factors negatively impacting contrast-medium injections and provides recommendations that can result in patient benefits, quality improvements, sustainability increases, and financial benefits by enabling otherwise unachievable optimization.</p><p><strong>Key points: </strong>How IV contrast media is administered is a rarely considered source of CT imaging variability. IV catheter selection, tubing length, injection systems, and insufficient flushing can result in unintended variability. These findings can be immediately addressed to improve standardization in contrast-enhanced CT imaging.</p>","PeriodicalId":13639,"journal":{"name":"Insights into Imaging","volume":"15 1","pages":"219"},"PeriodicalIF":4.1,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11358578/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142080161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Different radiomics annotation methods comparison in rectal cancer characterisation and prognosis prediction: a two-centre study. 直肠癌特征描述和预后预测中不同放射组学注释方法的比较:一项双中心研究。
IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-08-26 DOI: 10.1186/s13244-024-01795-5
Ying Zhu, Yaru Wei, Zhongwei Chen, Xiang Li, Shiwei Zhang, Caiyun Wen, Guoquan Cao, Jiejie Zhou, Meihao Wang

Objectives: To explore the performance differences of multiple annotations in radiomics analysis and provide a reference for tumour annotation in large-scale medical image analysis.

Methods: A total of 342 patients from two centres who underwent radical resection for rectal cancer were retrospectively studied and divided into training, internal validation, and external validation cohorts. Three predictive tasks of tumour T-stage (pT), lymph node metastasis (pLNM), and disease-free survival (pDFS) were performed. Twelve radiomics models were constructed using Lasso-Logistic or Lasso-Cox to evaluate and four annotation methods, 2D detailed annotation along tumour boundaries (2D), 3D detailed annotation along tumour boundaries (3D), 2D bounding box (2DBB), and 3D bounding box (3DBB) on T2-weighted images, were compared. Radiomics models were used to establish combined models incorporating clinical risk factors. The DeLong test was performed to compare the performance of models using the receiver operating characteristic curves.

Results: For radiomics models, the area under the curve values ranged from 0.627 (0.518-0.728) to 0.811 (0.705-0.917) in the internal validation cohort and from 0.619 (0.469-0.754) to 0.824 (0.689-0.918) in the external validation cohort. Most radiomics models based on four annotations did not differ significantly, except between the 3D and 3DBB models for pLNM (p = 0.0188) in the internal validation cohort. For combined models, only the 2D model significantly differed from the 2DBB (p = 0.0372) and 3D models (p = 0.0380) for pDFS.

Conclusion: Radiomics and combined models constructed with 2D and bounding box annotations showed comparable performances to those with 3D and detailed annotations along tumour boundaries in rectal cancer characterisation and prognosis prediction.

Critical relevance statement: For quantitative analysis of radiological images, the selection of 2D maximum tumour area or bounding box annotation is as representative and easy to operate as 3D whole tumour or detailed annotations along tumour boundaries.

Key points: There is currently a lack of discussion on whether different annotation efforts in radiomics are predictively representative. No significant differences were observed in radiomics and combined models regardless of the annotations (2D, 3D, detailed, or bounding box). Prioritise selecting the more time and effort-saving 2D maximum area bounding box annotation.

目的探讨放射组学分析中多种注释的性能差异,为大规模医学图像分析中的肿瘤注释提供参考:方法:对两个中心共 342 名接受直肠癌根治术的患者进行回顾性研究,并将其分为训练组、内部验证组和外部验证组。进行了肿瘤T期(pT)、淋巴结转移(pLNM)和无病生存(pDFS)三项预测任务。使用 Lasso-Logistic 或 Lasso-Cox 构建了 12 个放射组学模型进行评估,并比较了四种注释方法:沿肿瘤边界的二维详细注释(2D)、沿肿瘤边界的三维详细注释(3D)、T2 加权图像上的二维边界框(2DBB)和三维边界框(3DBB)。放射组学模型用于建立包含临床风险因素的综合模型。使用接收者操作特征曲线进行DeLong检验,以比较模型的性能:对于放射组学模型,内部验证队列的曲线下面积值从 0.627(0.518-0.728)到 0.811(0.705-0.917)不等,外部验证队列的曲线下面积值从 0.619(0.469-0.754)到 0.824(0.689-0.918)不等。除了内部验证队列中 pLNM 的 3D 和 3DBB 模型之间的差异(p = 0.0188)外,大多数基于四种注释的放射组学模型没有显著差异。就组合模型而言,只有 2D 模型与 2DBB 模型(p = 0.0372)和 3D 模型(p = 0.0380)在 pDFS 方面存在显著差异:结论:在直肠癌特征描述和预后预测方面,使用二维和边界框注释构建的放射组学模型和组合模型与使用三维和肿瘤边界详细注释构建的模型性能相当:对于放射图像的定量分析,选择二维最大肿瘤面积或边界框注释与三维全肿瘤或沿肿瘤边界的详细注释一样具有代表性且易于操作:要点:关于放射组学中不同的注释方法是否具有预测代表性,目前还缺乏讨论。无论采用何种注释方式(二维、三维、详细注释或边界框),在放射组学和组合模型中均未观察到明显差异。优先选择更省时省力的二维最大面积边界框注释。
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引用次数: 0
Publishing in open access journals. 在开放存取期刊上发表文章。
IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-08-26 DOI: 10.1186/s13244-024-01794-6
Emilio Quaia, Chiara Zanon, Alberto Vieira, Christian Loewe, Luis Marti-Bonmatí
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引用次数: 0
Digital breast tomosynthesis in breast cancer screening: an ethical perspective. 数字乳腺断层合成技术在乳腺癌筛查中的应用:伦理视角。
IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-08-26 DOI: 10.1186/s13244-024-01790-w
Simon Rosenqvist, Johan Brännmark, Magnus Dustler

Although digital breast tomosynthesis has higher sensitivity than digital mammography and at least as high specificity, digital mammography remains the most common method for conducting mammographic screening. At the same time, mammography systems are now delivered "DBT-ready" and can be used for either digital mammography or digital breast tomosynthesis. In this paper, we ask whether it is ethically permissible to use such equipment for digital mammography, given its lower sensitivity. We argue it is not, and that clinics are ethically required to use their DBT-ready equipment to screen with digital breast tomosynthesis whenever this is practically possible. Our argument relies on a comparison between digital breast tomosynthesis and a hypothesized improvement in the image quality of digital mammography. CRITICAL RELEVANCE STATEMENT: Women may lose out on the benefits of screening with digital breast tomosynthesis when DBT-ready equipment is used to screen with digital mammography; we argue that this practice is ethically problematic. KEY POINTS: Digital breast tomosynthesis finds more cases of breast cancer than digital mammography. Mammography equipment can often be used to screen with both digital breast tomosynthesis and digital mammography. When they can, clinics are ethically required to use existing equipment to screen with digital breast tomosynthesis instead of digital mammography.

尽管数字乳腺断层合成技术的灵敏度高于数字乳腺 X 光摄影技术,特异性也至少与之相当,但数字乳腺 X 光摄影技术仍是进行乳腺 X 光摄影筛查的最常用方法。与此同时,乳腺 X 射线摄影系统现在已经可以 "DBT 就绪",既可用于数字乳腺 X 射线摄影,也可用于数字乳腺断层合成。在本文中,我们要问的是,鉴于数字乳腺 X 射线摄影的灵敏度较低,在伦理上是否允许将此类设备用于数字乳腺 X 射线摄影。我们认为这是不允许的,而且在实际可行的情况下,诊所在伦理上必须使用可用于 DBT 的设备进行数字乳腺断层合成检查。我们的论点依赖于数字乳腺断层合成术与数字乳腺 X 射线摄影图像质量假设改进之间的比较。关键相关性声明:如果使用可进行 DBT 的设备进行数字乳腺 X 射线摄影筛查,妇女可能会失去数字乳腺断层摄影筛查的好处;我们认为这种做法在伦理上存在问题。要点:与数字乳腺 X 射线摄影相比,数字乳腺断层合成技术能发现更多的乳腺癌病例。乳腺 X 射线摄影设备通常可同时用于数字乳腺断层摄影和数字乳腺 X 射线摄影筛查。在可以使用的情况下,诊所应根据道德要求使用现有设备进行数字乳腺断层合成术筛查,而不是数字乳腺X光造影术。
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引用次数: 0
Prediction of extracapsular extension of prostate cancer by MRI radiomic signature: a systematic review. 通过磁共振成像放射学特征预测前列腺癌的囊外扩展:系统综述。
IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-08-26 DOI: 10.1186/s13244-024-01776-8
Adalgisa Guerra, Helen Wang, Matthew R Orton, Marianna Konidari, Nickolas K Papanikolaou, Dow Mu Koh, Helena Donato, Filipe Caseiro Alves

The objective of this review is to survey radiomics signatures for detecting pathological extracapsular extension (pECE) on magnetic resonance imaging (MRI) in patients with prostate cancer (PCa) who underwent prostatectomy. Scientific Literature databases were used to search studies published from January 2007 to October 2023. All studies related to PCa MRI staging and using radiomics signatures to detect pECE after prostatectomy were included. Systematic review was performed according to Preferred Reporting Items for Systematic Review and Meta-analyses (PRISMA). The risk of bias and certainty of the evidence was assessed using QUADAS-2 and the radiomics quality score. From 1247 article titles screened, 16 reports were assessed for eligibility, and 11 studies were included in this systematic review. All used a retrospective study design and most of them used 3 T MRI. Only two studies were performed in more than one institution. The highest AUC of a model using only radiomics features was 0.85, for the test validation. The AUC for best model performance (radiomics associated with clinical/semantic features) varied from 0.72-0.92 and 0.69-0.89 for the training and validation group, respectively. Combined models performed better than radiomics signatures alone for detecting ECE. Most of the studies showed a low to medium risk of bias. After thorough analysis, we found no strong evidence supporting the clinical use of radiomics signatures for identifying extracapsular extension (ECE) in pre-surgery PCa patients. Future studies should adopt prospective multicentre approaches using large public datasets and combined models for detecting ECE.

Critical relevant statement: The use of radiomics algorithms, with clinical and AI integration, in predicting extracapsular extension, could lead to the development of more accurate predictive models, which could help improve surgical planning and lead to better outcomes for prostate cancer patients.

Protocol of systematic review registration: PROSPERO CRD42021272088. Published: https://doi.org/10.1136/bmjopen-2021-052342 .

Key points: Radiomics can extract diagnostic features from MRI to enhance prostate cancer diagnosis performance. The combined models performed better than radiomics signatures alone for detecting extracapsular extension. Radiomics are not yet reliable for extracapsular detection in PCa patients.

本综述旨在调查磁共振成像(MRI)上检测接受前列腺切除术的前列腺癌(PCa)患者病理囊外扩展(pECE)的放射组学特征。使用科学文献数据库搜索 2007 年 1 月至 2023 年 10 月期间发表的研究。纳入了所有与 PCa MRI 分期和使用放射组学特征检测前列腺切除术后 pECE 相关的研究。根据《系统综述和荟萃分析首选报告项目》(Preferred Reporting Items for Systematic Review and Meta-analyses,PRISMA)进行系统综述。采用QUADAS-2和放射组学质量评分对证据的偏倚风险和确定性进行评估。从筛选出的 1247 篇文章标题中,有 16 篇报告通过了资格评估,11 项研究被纳入本系统综述。所有研究均采用回顾性研究设计,其中大部分使用 3 T MRI。只有两项研究是在一家以上的机构进行的。在测试验证中,仅使用放射组学特征的模型的最高 AUC 为 0.85。在训练组和验证组中,最佳模型性能(放射组学与临床/语义特征相关)的 AUC 分别为 0.72-0.92 和 0.69-0.89 不等。在检测 ECE 方面,组合模型的表现优于单独的放射组学特征。大多数研究显示存在低至中等程度的偏倚风险。经过全面分析,我们发现没有强有力的证据支持放射组学特征在临床上用于识别手术前PCa患者的囊外扩展(ECE)。未来的研究应采用前瞻性多中心方法,使用大型公共数据集和组合模型来检测ECE:将放射组学算法与临床和人工智能相结合,用于预测囊外扩展,可以开发出更准确的预测模型,有助于改善手术规划,为前列腺癌患者带来更好的治疗效果:系统综述注册协议:PREMCO CRD42021272088。发表于:https://doi.org/10.1136/bmjopen-2021-052342 .关键点:放射组学能从核磁共振成像中提取诊断特征,从而提高前列腺癌的诊断效果。在检测囊外扩展方面,联合模型的表现优于单独的放射组学特征。放射组学在PCa患者的囊外检测方面尚不可靠。
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引用次数: 0
Decoding MRI-informed brain age using mutual information. 利用互信息解码磁共振成像显示的大脑年龄
IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Pub Date : 2024-08-26 DOI: 10.1186/s13244-024-01791-9
Jing Li, Linda Chiu Wa Lam, Hanna Lu

Objective: We aimed to develop a standardized method to investigate the relationship between estimated brain age and regional morphometric features, meeting the criteria for simplicity, generalization, and intuitive interpretability.

Methods: We utilized T1-weighted magnetic resonance imaging (MRI) data from the Cambridge Centre for Ageing and Neuroscience project (N = 609) and employed a support vector regression method to train a brain age model. The pre-trained brain age model was applied to the dataset of the brain development project (N = 547). Kraskov (KSG) estimator was used to compute the mutual information (MI) value between brain age and regional morphometric features, including gray matter volume (GMV), white matter volume (WMV), cerebrospinal fluid (CSF) volume, and cortical thickness (CT).

Results: Among four types of brain features, GMV had the highest MI value (8.71), peaking in the pre-central gyrus (0.69). CSF volume was ranked second (7.76), with the highest MI value in the cingulate (0.87). CT was ranked third (6.22), with the highest MI value in superior temporal gyrus (0.53). WMV had the lowest MI value (4.59), with the insula showing the highest MI value (0.53). For brain parenchyma, the volume of the superior frontal gyrus exhibited the highest MI value (0.80).

Conclusion: This is the first demonstration that MI value between estimated brain age and morphometric features may serve as a benchmark for assessing the regional contributions to estimated brain age. Our findings highlighted that both GMV and CSF are the key features that determined the estimated brain age, which may add value to existing computational models of brain age.

Critical relevance statement: Mutual information (MI) analysis reveals gray matter volume (GMV) and cerebrospinal fluid (CSF) volume as pivotal in computing individuals' brain age.

Key points: Mutual information (MI) interprets estimated brain age with morphometric features. Gray matter volume in the pre-central gyrus has the highest MI value for estimated brain age. Cerebrospinal fluid volume in the cingulate has the highest MI value. Regarding brain parenchymal volume, the superior frontal gyrus has the highest MI value. The value of mutual information underscores the key brain regions related to brain age.

目的:我们旨在开发一种标准化方法,用于研究估计脑年龄与区域形态特征之间的关系:我们旨在开发一种标准化方法来研究估计脑年龄与区域形态特征之间的关系,该方法应符合简便性、通用性和直观可解释性的标准:我们利用剑桥老龄化与神经科学中心项目(N = 609)的 T1 加权磁共振成像(MRI)数据,采用支持向量回归法训练脑年龄模型。预先训练好的脑年龄模型被应用于大脑发育项目的数据集(N = 547)。使用Kraskov(KSG)估计器计算脑年龄与灰质体积(GMV)、白质体积(WMV)、脑脊液体积(CSF)和皮质厚度(CT)等区域形态特征之间的互信息(MI)值:在四种大脑特征中,灰质体积的 MI 值最高(8.71),在中央前回达到峰值(0.69)。脑脊液体积排名第二(7.76),扣带回的 MI 值最高(0.87)。CT 排名第三(6.22),颞上回的 MI 值最高(0.53)。WMV的MI值最低(4.59),岛叶的MI值最高(0.53)。就大脑实质而言,额上回的体积显示出最高的 MI 值(0.80):这是首次证明估计脑年龄与形态特征之间的 MI 值可作为评估区域对估计脑年龄贡献的基准。我们的研究结果突出表明,GMV 和 CSF 是决定估计脑年龄的关键特征,这可能会增加现有脑年龄计算模型的价值:互信息(MI)分析揭示了灰质体积(GMV)和脑脊液(CSF)体积在计算个人脑年龄中的关键作用:要点:互信息(MI)通过形态特征来解释估计的脑年龄。中央前回的灰质体积对估计脑年龄的互信息值最高。扣带回的脑脊液体积具有最高的 MI 值。在脑实质体积方面,额上回的 MI 值最高。互信息值强调了与脑年龄相关的关键脑区。
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Insights into Imaging
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