Pub Date : 2025-11-05DOI: 10.1186/s41747-025-00649-z
Xiaowei Huang, Xian Gu
{"title":"Letter to the Editor: Advancing deep learning-based segmentation for multiple lung cancer lesions in real-world multicenter CT scans.","authors":"Xiaowei Huang, Xian Gu","doi":"10.1186/s41747-025-00649-z","DOIUrl":"10.1186/s41747-025-00649-z","url":null,"abstract":"","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"110"},"PeriodicalIF":3.6,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12589690/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145446053","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-05DOI: 10.1186/s41747-025-00650-6
Xavier Rafael-Palou, Ana Jimenez-Pastor, Luis Marti-Bonmati, Carlos F Muñoz-Nuñez, Mario Laudazi, Angel Alberich-Bayarri
{"title":"Reply to the letter to the Editor: Advancing deep learning-based segmentation for multiple lung cancer lesions in real-world multicenter CT scans.","authors":"Xavier Rafael-Palou, Ana Jimenez-Pastor, Luis Marti-Bonmati, Carlos F Muñoz-Nuñez, Mario Laudazi, Angel Alberich-Bayarri","doi":"10.1186/s41747-025-00650-6","DOIUrl":"10.1186/s41747-025-00650-6","url":null,"abstract":"","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"109"},"PeriodicalIF":3.6,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12589689/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145445989","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Amyotrophic lateral sclerosis (ALS) is a progressive motor neuron disease with peripheral nerve involvement, but current diagnostics are limited. Diffusion tensor imaging (DTI) may improve microstructural assessment and correlate with clinical markers. We investigated the diffusion properties of the brachial plexus in ALS and examined their relationships with electrophysiological parameters of upper limb nerves.
Materials and methods: We enrolled 25 ALS patients and 22 age- and sex-matched healthy controls. DTI of the brachial plexus was conducted to measure fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD). Differences in DTI parameters between the two groups were analyzed. Correlations between DTI parameters and ALS Functional Rating Scale-Revised (ALSFRS-R) scores, along with electrophysiological measurements, were assessed.
Results: In ALS patients compared to controls, FA and AD values were significantly lower (p ≤ 0.002), while the RD value was significantly higher (p = 0.002). There were no statistically significant differences in MD (p = 0.540). Both FA and AD showed a positive correlation with ALSFRS-R score, ALSFRS-upper limb score, and compound muscle action potential amplitude of median, ulnar, and radial nerves (r ≥ 0.480; p ≤ 0.015). The RD values showed a negative correlation with ALSFRS-upper limb score and motor nerve conduction velocity of median, ulnar, and radial nerves (r ≤ -0.415; p ≤ 0.039).
Conclusion: FA, AD, and RD values of DTI showed the potential to identify microstructural changes in the brachial plexus nerve roots of ALS patients and may serve as potential indicators of nerve conduction function in the upper extremities.
Relevance statement: DTI may reveal microstructural changes in ALS brachial plexus, correlating with nerve dysfunction, offering novel biomarkers for evaluation of upper limb neurodegeneration.
Key points: Lower Fractional anisotropy (FA) and axial diffusivity (AD), and higher radial diffusivity (RD) were shown in amyotrophic lateral sclerosis (ALS) brachial plexus. Diffusion tensor imaging (DTI) parameters correlated with clinical and electrophysiological parameters. FA, AD, and RD detected ALS nerve microstructural changes, indicating abnormal conduction function.
{"title":"DTI changes of brachial plexus nerve roots in amyotrophic lateral sclerosis and their correlation with electrophysiology.","authors":"Shanshan Wang, Yuxin Li, Xuewen Xing, Xiao Man, Yufan Chen, Guangbin Wang","doi":"10.1186/s41747-025-00645-3","DOIUrl":"10.1186/s41747-025-00645-3","url":null,"abstract":"<p><strong>Background: </strong>Amyotrophic lateral sclerosis (ALS) is a progressive motor neuron disease with peripheral nerve involvement, but current diagnostics are limited. Diffusion tensor imaging (DTI) may improve microstructural assessment and correlate with clinical markers. We investigated the diffusion properties of the brachial plexus in ALS and examined their relationships with electrophysiological parameters of upper limb nerves.</p><p><strong>Materials and methods: </strong>We enrolled 25 ALS patients and 22 age- and sex-matched healthy controls. DTI of the brachial plexus was conducted to measure fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD). Differences in DTI parameters between the two groups were analyzed. Correlations between DTI parameters and ALS Functional Rating Scale-Revised (ALSFRS-R) scores, along with electrophysiological measurements, were assessed.</p><p><strong>Results: </strong>In ALS patients compared to controls, FA and AD values were significantly lower (p ≤ 0.002), while the RD value was significantly higher (p = 0.002). There were no statistically significant differences in MD (p = 0.540). Both FA and AD showed a positive correlation with ALSFRS-R score, ALSFRS-upper limb score, and compound muscle action potential amplitude of median, ulnar, and radial nerves (r ≥ 0.480; p ≤ 0.015). The RD values showed a negative correlation with ALSFRS-upper limb score and motor nerve conduction velocity of median, ulnar, and radial nerves (r ≤ -0.415; p ≤ 0.039).</p><p><strong>Conclusion: </strong>FA, AD, and RD values of DTI showed the potential to identify microstructural changes in the brachial plexus nerve roots of ALS patients and may serve as potential indicators of nerve conduction function in the upper extremities.</p><p><strong>Relevance statement: </strong>DTI may reveal microstructural changes in ALS brachial plexus, correlating with nerve dysfunction, offering novel biomarkers for evaluation of upper limb neurodegeneration.</p><p><strong>Key points: </strong>Lower Fractional anisotropy (FA) and axial diffusivity (AD), and higher radial diffusivity (RD) were shown in amyotrophic lateral sclerosis (ALS) brachial plexus. Diffusion tensor imaging (DTI) parameters correlated with clinical and electrophysiological parameters. FA, AD, and RD detected ALS nerve microstructural changes, indicating abnormal conduction function.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"107"},"PeriodicalIF":3.6,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12586801/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145446021","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-04DOI: 10.1186/s41747-025-00644-4
Louise D'hondt, Dimitri Buytaert, Pieter-Jan Kellens, Annemiek Snoeckx, Klaus Bacher
<p><strong>Background: </strong>Oversimplified pulmonary nodule phantoms limit the clinical translation of computed tomography (CT) research. Therefore, we manufactured and preliminarily validated patient-realistic part-solid nodule models with heterogeneous radiodensities using a stereolithography apparatus (SLA) benchtop three-dimensional (3D) printing.</p><p><strong>Materials and methods: </strong>Patient-derived CT images were utilised upon Ethics Committee approval to determine part-solid nodule HU ranges and morphologies. To lower the density of the applied resin (Formlabs Clear V4), we designed variable 3D-beams (340, 510, or 680 µm) into lattice structures with variable gap thicknesses (from 680 to 2,040 µm). These lattice structures were merged with patient-derived nodule segmentations. The 3D-prints were incorporated in a Lungman phantom and evaluated using low-dose CT imaging. A multicentre, single-blinded reader study, involving seventeen radiologists, assessed whether 3D-printed nodules were distinguishable from real part-solid nodules using χ<sup>2</sup> goodness-of-fit testing.</p><p><strong>Results: </strong>Through varying combinations of material thicknesses and void sizes, we reproduced multiple target radiodensities of clinical nodules and successfully manufactured pulmonary nodule phantoms consisting of three different ground-glass components around a solidly printed core. There was significant evidence (χ<sup>2</sup> = 136.13; p = 1.864e-31; 5% confidence level) against readers reliably distinguishing patient nodules from our 3D-printed models. Average accuracy across all radiologists was 53.5%. Moreover, 47.5% of the 3D-printed nodules were incorrectly classified as real nodules.</p><p><strong>Conclusion: </strong>Our SLA 3D-printing workflow produces patient-realistic part-solid pulmonary nodules that are more cost-effective than commercially available counterparts. This methodology could provide customisable ground truth phantom models for CT imaging studies, including software validation, acquisition and reconstruction parameter optimisation and/or image quality evaluation.</p><p><strong>Relevance statement: </strong>This study marks the first successful application of SLA 3D-printing to manufacture part-solid pulmonary nodule phantoms, incorporating multiple radiodensities and mimicking patient-realistic morphologies. Our developed methodology offers potential to 3D-printed phantoms with higher degrees of customisation and adaptation to research-specific objectives in CT imaging compared to commercially available standardised phantoms.</p><p><strong>Key points: </strong>Part-solid pulmonary nodule phantoms with patient-realistic morphologies and multiple radiodensities were manufactured using benchtop SLA 3D-printing. Clinical relevance of our 3D-printed nodules is demonstrated and statistically substantiated in a multicentre, single-blinded reader study including seventeen reading radiologists. Our methodology renders
背景:过度简化的肺结节影限制了计算机断层扫描(CT)研究的临床转化。因此,我们使用立体光刻设备(SLA)台式三维(3D)打印制造并初步验证了具有非均匀放射密度的患者真实部分-实体结节模型。材料和方法:经伦理委员会批准,使用患者CT图像确定部分实性结节的HU范围和形态。为了降低所应用树脂(Formlabs Clear V4)的密度,我们将可变3d梁(340、510或680µm)设计成具有可变间隙厚度(680至2040µm)的晶格结构。这些点阵结构与患者衍生的结节分割合并。将3d打印物与Lungman假体结合,并使用低剂量CT成像进行评估。一项涉及17名放射科医生的多中心单盲阅读研究,使用χ2拟合优度检验评估3d打印结节是否与真实的部分实性结节区分开来。结果:通过不同材料厚度和空洞大小的组合,我们复制了临床结节的多个目标放射密度,并成功地制造了由三种不同的毛玻璃成分组成的肺结节幻象,围绕着固体打印的核心。有显著证据(χ2 = 136.13; p = 1.864e-31; 5%置信水平)表明,读取器能够可靠地将患者结节与我们的3d打印模型区分开来。所有放射科医生的平均准确率为53.5%。此外,47.5%的3d打印结节被错误地归类为真正的结节。结论:我们的SLA 3d打印工作流程产生了患者真实的部分实性肺结节,比市售的同行更具成本效益。该方法可以为CT成像研究提供可定制的ground truth phantom模型,包括软件验证、采集和重建参数优化和/或图像质量评估。相关声明:本研究标志着SLA 3d打印首次成功应用于制造部分实性肺结节幻象,结合多种放射密度并模仿患者真实的形态。与商业上可用的标准化模型相比,我们开发的方法为3d打印模型提供了更高程度的定制和适应CT成像研究特定目标的潜力。重点:采用台式SLA 3d打印技术制造具有患者真实形态和多重放射密度的部分实性肺结节幻象。我们的3d打印结节的临床相关性在一项包括17名阅读放射科医生在内的多中心单盲阅读研究中得到了证明和统计证实。我们的方法使肺结节模型克服了通用的、标准化的、商业上可用的模型的局限性,这些模型通常缺乏复杂性和真实感。人造结节模型可以为软件培训和验证、CT方案优化和(图像)质量保证提供绝对的基础事实。我们改进的3d打印方法很容易被其他团体使用,并且可以根据特定的研究应用进行定制。
{"title":"Part-solid pulmonary nodule phantoms with realistic morphology and densities by stereolithography-based 3D-printing: from design to validation.","authors":"Louise D'hondt, Dimitri Buytaert, Pieter-Jan Kellens, Annemiek Snoeckx, Klaus Bacher","doi":"10.1186/s41747-025-00644-4","DOIUrl":"10.1186/s41747-025-00644-4","url":null,"abstract":"<p><strong>Background: </strong>Oversimplified pulmonary nodule phantoms limit the clinical translation of computed tomography (CT) research. Therefore, we manufactured and preliminarily validated patient-realistic part-solid nodule models with heterogeneous radiodensities using a stereolithography apparatus (SLA) benchtop three-dimensional (3D) printing.</p><p><strong>Materials and methods: </strong>Patient-derived CT images were utilised upon Ethics Committee approval to determine part-solid nodule HU ranges and morphologies. To lower the density of the applied resin (Formlabs Clear V4), we designed variable 3D-beams (340, 510, or 680 µm) into lattice structures with variable gap thicknesses (from 680 to 2,040 µm). These lattice structures were merged with patient-derived nodule segmentations. The 3D-prints were incorporated in a Lungman phantom and evaluated using low-dose CT imaging. A multicentre, single-blinded reader study, involving seventeen radiologists, assessed whether 3D-printed nodules were distinguishable from real part-solid nodules using χ<sup>2</sup> goodness-of-fit testing.</p><p><strong>Results: </strong>Through varying combinations of material thicknesses and void sizes, we reproduced multiple target radiodensities of clinical nodules and successfully manufactured pulmonary nodule phantoms consisting of three different ground-glass components around a solidly printed core. There was significant evidence (χ<sup>2</sup> = 136.13; p = 1.864e-31; 5% confidence level) against readers reliably distinguishing patient nodules from our 3D-printed models. Average accuracy across all radiologists was 53.5%. Moreover, 47.5% of the 3D-printed nodules were incorrectly classified as real nodules.</p><p><strong>Conclusion: </strong>Our SLA 3D-printing workflow produces patient-realistic part-solid pulmonary nodules that are more cost-effective than commercially available counterparts. This methodology could provide customisable ground truth phantom models for CT imaging studies, including software validation, acquisition and reconstruction parameter optimisation and/or image quality evaluation.</p><p><strong>Relevance statement: </strong>This study marks the first successful application of SLA 3D-printing to manufacture part-solid pulmonary nodule phantoms, incorporating multiple radiodensities and mimicking patient-realistic morphologies. Our developed methodology offers potential to 3D-printed phantoms with higher degrees of customisation and adaptation to research-specific objectives in CT imaging compared to commercially available standardised phantoms.</p><p><strong>Key points: </strong>Part-solid pulmonary nodule phantoms with patient-realistic morphologies and multiple radiodensities were manufactured using benchtop SLA 3D-printing. Clinical relevance of our 3D-printed nodules is demonstrated and statistically substantiated in a multicentre, single-blinded reader study including seventeen reading radiologists. Our methodology renders ","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"106"},"PeriodicalIF":3.6,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12586819/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145439439","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-04DOI: 10.1186/s41747-025-00646-2
Renée M Girbig, Anne Rix, Jasmin Baier, Leonie Tix, Anna M Hartmann, Wenjia Liu, Pascal Paschenda, Alexandru Florea, Masoud Sadeghzadeh, Karolin Becker, Rupert Palme, Felix M Mottaghy, René Tolba, Fabian Kiessling
Background: Pain assessment in animal models is challenging, as behavioral tests often lack sensitivity. Particularly under analgesia, it is unclear whether pain occurs without medication. Imaging of pain-associated pathways, such as σ1 receptor (σ1R) expression, offers a promising approach to better understand underlying mechanisms. Therefore, this study evaluated [¹⁸F]fluspidine positron emission tomography/computed tomography (PET/CT) imaging for detecting σ1R-mediated pain after partial liver resection in rats.
Materials and methods: Postoperative pain was assessed in eighteen female Wistar rats undergoing skin incision or partial liver resection. Nine untreated rats served as controls. Carprofen was administered for three consecutive days after surgery. PET/CT imaging was performed on postoperative days 1, 4, and 7. At each time point, organs and incision sites of three animals were harvested for histological analysis. Postoperative pain and welfare were monitored by observational score sheets, the Open Field test, Rat Grimace Scale, Von Frey test, fecal corticosterone metabolites, and hemograms.
Results: Despite analgesic treatment, PET/CT and immunohistochemistry revealed elevated σ1R expression at the abdominal incision site on day 1 after partial liver resection in comparison to the other groups, likely due to the additional peritoneal opening. σ1R expression normalized by day 4. No behavioral indicators of pain or distress were observed, though mechanical hypersensitivity was detected on day 4 in all groups, likely due to carprofen side effects.
Conclusion: [18F]Fluspidine PET/CT imaging sensitively detected postoperative pain-associated σ1R expression independent of analgesia. This imaging modality could remarkably refine pain monitoring, opening to further studies using different pain and analgesia models.
Relevance statement: [¹⁸F]Fluspidine PET/CT imaging demonstrates high sensitivity in detecting pain-associated σ1R upregulation despite non-steroidal anti-inflammatory drug administration. This approach offers valuable insights for refining pain assessment, improving severity grading, and enhancing the reliability and translational value of preclinical pain models.
Key points: PET/CT imaging with [18F]fluspidine sensitively detects pain-associated σ1R expression post-liver resection. Necessary analgesia interferes with some behavioral tests, limiting their reliability for pain assessment. [18F]Fluspidine detects peripheral σ1R upregulation despite non-steroidal anti-inflammatory drug analgesia. Imaging pain-associated receptors provides valuable insights for refining preclinical pain monitoring.
{"title":"[¹⁸F]Fluspidine PET/CT imaging to assess postoperative pain-associated σ1 receptor expression in female rats under analgesia.","authors":"Renée M Girbig, Anne Rix, Jasmin Baier, Leonie Tix, Anna M Hartmann, Wenjia Liu, Pascal Paschenda, Alexandru Florea, Masoud Sadeghzadeh, Karolin Becker, Rupert Palme, Felix M Mottaghy, René Tolba, Fabian Kiessling","doi":"10.1186/s41747-025-00646-2","DOIUrl":"10.1186/s41747-025-00646-2","url":null,"abstract":"<p><strong>Background: </strong>Pain assessment in animal models is challenging, as behavioral tests often lack sensitivity. Particularly under analgesia, it is unclear whether pain occurs without medication. Imaging of pain-associated pathways, such as σ1 receptor (σ1R) expression, offers a promising approach to better understand underlying mechanisms. Therefore, this study evaluated [¹⁸F]fluspidine positron emission tomography/computed tomography (PET/CT) imaging for detecting σ1R-mediated pain after partial liver resection in rats.</p><p><strong>Materials and methods: </strong>Postoperative pain was assessed in eighteen female Wistar rats undergoing skin incision or partial liver resection. Nine untreated rats served as controls. Carprofen was administered for three consecutive days after surgery. PET/CT imaging was performed on postoperative days 1, 4, and 7. At each time point, organs and incision sites of three animals were harvested for histological analysis. Postoperative pain and welfare were monitored by observational score sheets, the Open Field test, Rat Grimace Scale, Von Frey test, fecal corticosterone metabolites, and hemograms.</p><p><strong>Results: </strong>Despite analgesic treatment, PET/CT and immunohistochemistry revealed elevated σ1R expression at the abdominal incision site on day 1 after partial liver resection in comparison to the other groups, likely due to the additional peritoneal opening. σ1R expression normalized by day 4. No behavioral indicators of pain or distress were observed, though mechanical hypersensitivity was detected on day 4 in all groups, likely due to carprofen side effects.</p><p><strong>Conclusion: </strong>[<sup>18</sup>F]Fluspidine PET/CT imaging sensitively detected postoperative pain-associated σ1R expression independent of analgesia. This imaging modality could remarkably refine pain monitoring, opening to further studies using different pain and analgesia models.</p><p><strong>Relevance statement: </strong>[¹⁸F]Fluspidine PET/CT imaging demonstrates high sensitivity in detecting pain-associated σ1R upregulation despite non-steroidal anti-inflammatory drug administration. This approach offers valuable insights for refining pain assessment, improving severity grading, and enhancing the reliability and translational value of preclinical pain models.</p><p><strong>Key points: </strong>PET/CT imaging with [<sup>18</sup>F]fluspidine sensitively detects pain-associated σ1R expression post-liver resection. Necessary analgesia interferes with some behavioral tests, limiting their reliability for pain assessment. [<sup>18</sup>F]Fluspidine detects peripheral σ1R upregulation despite non-steroidal anti-inflammatory drug analgesia. Imaging pain-associated receptors provides valuable insights for refining preclinical pain monitoring.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"108"},"PeriodicalIF":3.6,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12586836/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145446017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-03DOI: 10.1186/s41747-025-00641-7
Gisella Gennaro, Moreno Zanardo, Federico Ambrogi, Francesco Sardanelli
Phantom studies are essential in medical imaging, offering a controlled and reproducible framework for evaluating imaging technologies across all modalities. Phantoms, whether physical (synthetic, biological, or mixed) or computational, simulate human tissues or anatomical structures and serve roles in technology validation, performance benchmarking, protocol optimization, quality assurance, and artificial intelligence development. We provide recommendations for designing and conducting phantom studies in medical imaging (PSMI). Key aspects include phantom selection, image acquisition protocols, and analysis strategies, particularly when image quality is evaluated in relation to radiation dose or contrast agent optimization. Quantitative image analysis is considered with emphasis on signal-to-noise ratio, contrast-to-noise ratio, and spatial resolution (e.g., modulation transfer function). Qualitative assessment is addressed considering reader selection and training, blinding, randomization, and use of absolute or relative Likert scales. Brief recommendations for sample size calculation, data reporting, and statistical analysis are provided, covering continuous/ordinal data, inter-rater agreement, and group comparisons. A checklist is provided to allow authors to document adherence to these recommendations and to identify shortcomings, limitations, and weaknesses in their phantom studies. The PSMI checklist is proposed to promote transparency, reproducibility, and critical appraisal, containing 25 items regarding: title/abstract (1, 2); background/introduction (3); methods/study design (4); methods/phantom description (5-7); methods/imaging protocol (8, 9); methods/image analysis (10, 11); methods/statistics (12-15); results/quantitative analysis (16, 17); results/qualitative analysis (18); results/tables and figures (19); discussion (20-23); and conclusions (24, 25). Finally, the importance of maintaining a clinical perspective is underscored, highlighting how well-designed phantom studies can inform, but not replace, clinical validation. RELEVANCE STATEMENT: This paper provides comprehensive recommendations for designing and conducting PSMI. The use of the PSMI checklist may contribute to increasing the quality of phantom studies. KEY POINTS: Phantom studies provide controlled, reproducible evaluation of imaging technologies. Phantoms simulate human tissues for validation, optimization, and AI development. Good design includes proper phantom selection and analysis strategies. Clinical relevance must guide interpretation; phantoms cannot replace clinical validation. The proposed 25-item PSMI checklist supports transparent and reproducible phantom study reporting.
{"title":"Phantom studies in medical imaging (PSMI): a guide with recommendations and checklist.","authors":"Gisella Gennaro, Moreno Zanardo, Federico Ambrogi, Francesco Sardanelli","doi":"10.1186/s41747-025-00641-7","DOIUrl":"10.1186/s41747-025-00641-7","url":null,"abstract":"<p><p>Phantom studies are essential in medical imaging, offering a controlled and reproducible framework for evaluating imaging technologies across all modalities. Phantoms, whether physical (synthetic, biological, or mixed) or computational, simulate human tissues or anatomical structures and serve roles in technology validation, performance benchmarking, protocol optimization, quality assurance, and artificial intelligence development. We provide recommendations for designing and conducting phantom studies in medical imaging (PSMI). Key aspects include phantom selection, image acquisition protocols, and analysis strategies, particularly when image quality is evaluated in relation to radiation dose or contrast agent optimization. Quantitative image analysis is considered with emphasis on signal-to-noise ratio, contrast-to-noise ratio, and spatial resolution (e.g., modulation transfer function). Qualitative assessment is addressed considering reader selection and training, blinding, randomization, and use of absolute or relative Likert scales. Brief recommendations for sample size calculation, data reporting, and statistical analysis are provided, covering continuous/ordinal data, inter-rater agreement, and group comparisons. A checklist is provided to allow authors to document adherence to these recommendations and to identify shortcomings, limitations, and weaknesses in their phantom studies. The PSMI checklist is proposed to promote transparency, reproducibility, and critical appraisal, containing 25 items regarding: title/abstract (1, 2); background/introduction (3); methods/study design (4); methods/phantom description (5-7); methods/imaging protocol (8, 9); methods/image analysis (10, 11); methods/statistics (12-15); results/quantitative analysis (16, 17); results/qualitative analysis (18); results/tables and figures (19); discussion (20-23); and conclusions (24, 25). Finally, the importance of maintaining a clinical perspective is underscored, highlighting how well-designed phantom studies can inform, but not replace, clinical validation. RELEVANCE STATEMENT: This paper provides comprehensive recommendations for designing and conducting PSMI. The use of the PSMI checklist may contribute to increasing the quality of phantom studies. KEY POINTS: Phantom studies provide controlled, reproducible evaluation of imaging technologies. Phantoms simulate human tissues for validation, optimization, and AI development. Good design includes proper phantom selection and analysis strategies. Clinical relevance must guide interpretation; phantoms cannot replace clinical validation. The proposed 25-item PSMI checklist supports transparent and reproducible phantom study reporting.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"105"},"PeriodicalIF":3.6,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12583249/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145439456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-31DOI: 10.1186/s41747-025-00643-5
Takeshi Fukuda, Akira Ogihara, Takenori Yonenaga, Daisuke Kubota, Hiroteru Hayashi, Ryuichi Itou, Hisashi Kitagawa, Katsutosi Murata, Stefan Sommer
Background: We aimed to evaluate longitudinal changes in ultrashort echo time (UTE) two-component biomarkers reflecting graft ligamentization after anterior cruciate ligament (ACL) reconstruction and to identify associated clinical factors.
Materials and methods: Patients who underwent ACL reconstruction were prospectively included to perform 3-T three-dimensional double-echo UTE sequence at 3, 6, and 12 months postoperatively. Mean values of short T2* (T2*s), long T2* (T2*l), and fast fraction (FF), i.e., the signal proportion attributed to the T2*s component, were calculated by fitting a biexponential model. Changes were analyzed using repeated measures analysis of variance-ANOVA. Multiple linear regression was used to assess associations between clinical factors and UTE parameters at 12 months.
Results: Forty-two patients (20 males), aged 32.7 ± 15.0 years (mean ± standard deviation), were enrolled. T2*s and T2*l increased from 3 to 6 months (T2*s, 5.3 to 5.7 ms; p = 0.017; T2*l, 21.1 to 23.3 ms; p < 0.001), then decreased from 6 to 12 months (T2*s, 5.7 to 5.0 ms; T2*l, 23.3 to 21.1 ms; both p < 0.001). FF followed the opposite trend, decreasing from 0.29 to 0.25, then increasing to 0.30 (both p < 0.001). At 12 months, a higher body mass index (BMI) was associated with elevated T2*s (p = 0.005), while semitendinosus-gracilis (STG) grafts (p = 0.018) and remnant preservation (p = 0.004) were associated with lower T2*s values.
Conclusion: UTE two-component analysis captures temporal changes in graft after ACL reconstruction, suggesting collagen regeneration. Higher BMI may hinder, while STG grafts and remnant preservation may promote ligamentization.
Relevance statement: UTE two-component analysis serves as an imaging biomarker for ACL graft ligamentization, with higher BMI being associated with impaired ligamentization, while the use of STG grafts and remnant preservation may be associated with more favorable graft maturation at 12 months as assessed by UTE two-component MRI. These findings may help tailor rehabilitation protocols and guide graft selection.
Trial registration: This study was prospectively registered with the University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) under the identification number UMIN000045710 in October 2021.
Key points: Ultrashort echo time two-component analysis noninvasively evaluates ligamentization of reconstructed ACL. Graft short T2* significantly decreased between 6 and 12 months postoperatively. Body mass index, graft type, and remnant status may influence graft maturation at 12 months.
{"title":"Prospective UTE two-component MRI analysis of graft ligamentization after ACL reconstruction and association with demographic and surgical factors.","authors":"Takeshi Fukuda, Akira Ogihara, Takenori Yonenaga, Daisuke Kubota, Hiroteru Hayashi, Ryuichi Itou, Hisashi Kitagawa, Katsutosi Murata, Stefan Sommer","doi":"10.1186/s41747-025-00643-5","DOIUrl":"10.1186/s41747-025-00643-5","url":null,"abstract":"<p><strong>Background: </strong>We aimed to evaluate longitudinal changes in ultrashort echo time (UTE) two-component biomarkers reflecting graft ligamentization after anterior cruciate ligament (ACL) reconstruction and to identify associated clinical factors.</p><p><strong>Materials and methods: </strong>Patients who underwent ACL reconstruction were prospectively included to perform 3-T three-dimensional double-echo UTE sequence at 3, 6, and 12 months postoperatively. Mean values of short T2* (T2*<sub>s</sub>), long T2* (T2*<sub>l</sub>), and fast fraction (FF), i.e., the signal proportion attributed to the T2*<sub>s</sub> component, were calculated by fitting a biexponential model. Changes were analyzed using repeated measures analysis of variance-ANOVA. Multiple linear regression was used to assess associations between clinical factors and UTE parameters at 12 months.</p><p><strong>Results: </strong>Forty-two patients (20 males), aged 32.7 ± 15.0 years (mean ± standard deviation), were enrolled. T2*<sub>s</sub> and T2*<sub>l</sub> increased from 3 to 6 months (T2*<sub>s</sub>, 5.3 to 5.7 ms; p = 0.017; T2*<sub>l</sub>, 21.1 to 23.3 ms; p < 0.001), then decreased from 6 to 12 months (T2*<sub>s</sub>, 5.7 to 5.0 ms; T2*<sub>l</sub>, 23.3 to 21.1 ms; both p < 0.001). FF followed the opposite trend, decreasing from 0.29 to 0.25, then increasing to 0.30 (both p < 0.001). At 12 months, a higher body mass index (BMI) was associated with elevated T2*<sub>s</sub> (p = 0.005), while semitendinosus-gracilis (STG) grafts (p = 0.018) and remnant preservation (p = 0.004) were associated with lower T2*<sub>s</sub> values.</p><p><strong>Conclusion: </strong>UTE two-component analysis captures temporal changes in graft after ACL reconstruction, suggesting collagen regeneration. Higher BMI may hinder, while STG grafts and remnant preservation may promote ligamentization.</p><p><strong>Relevance statement: </strong>UTE two-component analysis serves as an imaging biomarker for ACL graft ligamentization, with higher BMI being associated with impaired ligamentization, while the use of STG grafts and remnant preservation may be associated with more favorable graft maturation at 12 months as assessed by UTE two-component MRI. These findings may help tailor rehabilitation protocols and guide graft selection.</p><p><strong>Trial registration: </strong>This study was prospectively registered with the University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) under the identification number UMIN000045710 in October 2021.</p><p><strong>Key points: </strong>Ultrashort echo time two-component analysis noninvasively evaluates ligamentization of reconstructed ACL. Graft short T2* significantly decreased between 6 and 12 months postoperatively. Body mass index, graft type, and remnant status may influence graft maturation at 12 months.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"104"},"PeriodicalIF":3.6,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12579095/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145423195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-23DOI: 10.1186/s41747-025-00638-2
Dmitrij Kravchenko, Muhammad Taha Hagar, Milan Vecsey-Nagy, Ildiko Kabat, Anne Groteklaes, Julian A Luetkens, Daniel Kuetting, Alexander Isaak, Tilman Emrich, Akos Varga-Szemes, Maria Vittoria Spampinato
Recent advances in magnetic resonance imaging (MRI) hardware and software have renewed interest in low-field MRI, challenging the long-held notion that such systems are inherently inferior to high-field counterparts. Traditionally dismissed due to lower signal-to-noise ratios and reduced image quality, low-field MRI was primarily relegated to cost-sensitive or resource-limited settings. However, modern low-field systems now integrate advanced reconstruction algorithms, refined imaging techniques, and improved hardware design, significantly narrowing the performance gap. In some scenarios, these systems offer distinct advantages, such as reduced susceptibility artifacts and improved safety of metallic implants. Their portability, lower operational costs, and reduced infrastructure demands make them especially valuable in point-of-care, remote, or intraoperative environments. This review examines the physical principles of low-field MRI, traces its technological evolution, and evaluates its current and emerging clinical applications. By highlighting both its strengths and limitations, we aim to clarify the growing role of low-field MRI in contemporary diagnostic imaging and underscore its potential in expanding global access to high-quality radiological care. RELEVANCE STATEMENT: Low-field and portable MRI systems offer a cost-effective, accessible, and safer imaging alternative that may expand diagnostic capabilities in underserved, point-of-care, and intraoperative settings, thereby improving global access to essential radiologic services. KEY POINTS: Advanced image reconstruction improves low-field MRI image quality and diagnostic utility. Reduced susceptibility artifacts enhance imaging near metallic hardware and air-tissue interfaces. Low-field systems enable cost-effective, portable imaging in constrained clinical environments.
{"title":"Low-field and portable MRI technology: advancements and innovations.","authors":"Dmitrij Kravchenko, Muhammad Taha Hagar, Milan Vecsey-Nagy, Ildiko Kabat, Anne Groteklaes, Julian A Luetkens, Daniel Kuetting, Alexander Isaak, Tilman Emrich, Akos Varga-Szemes, Maria Vittoria Spampinato","doi":"10.1186/s41747-025-00638-2","DOIUrl":"10.1186/s41747-025-00638-2","url":null,"abstract":"<p><p>Recent advances in magnetic resonance imaging (MRI) hardware and software have renewed interest in low-field MRI, challenging the long-held notion that such systems are inherently inferior to high-field counterparts. Traditionally dismissed due to lower signal-to-noise ratios and reduced image quality, low-field MRI was primarily relegated to cost-sensitive or resource-limited settings. However, modern low-field systems now integrate advanced reconstruction algorithms, refined imaging techniques, and improved hardware design, significantly narrowing the performance gap. In some scenarios, these systems offer distinct advantages, such as reduced susceptibility artifacts and improved safety of metallic implants. Their portability, lower operational costs, and reduced infrastructure demands make them especially valuable in point-of-care, remote, or intraoperative environments. This review examines the physical principles of low-field MRI, traces its technological evolution, and evaluates its current and emerging clinical applications. By highlighting both its strengths and limitations, we aim to clarify the growing role of low-field MRI in contemporary diagnostic imaging and underscore its potential in expanding global access to high-quality radiological care. RELEVANCE STATEMENT: Low-field and portable MRI systems offer a cost-effective, accessible, and safer imaging alternative that may expand diagnostic capabilities in underserved, point-of-care, and intraoperative settings, thereby improving global access to essential radiologic services. KEY POINTS: Advanced image reconstruction improves low-field MRI image quality and diagnostic utility. Reduced susceptibility artifacts enhance imaging near metallic hardware and air-tissue interfaces. Low-field systems enable cost-effective, portable imaging in constrained clinical environments.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"103"},"PeriodicalIF":3.6,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12549457/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1186/s41747-025-00640-8
Tobias Norajitra, Michael A Baumgartner, Lucas R Cusumano, Jesus G Ulloa, Christian S Rizzo, Florian Haag, Alexander Hertel, Nils A Rathmann, Steffen J Diehl, Stefan O Schoenberg, Klaus H Maier-Hein, Johann S Rink
Background: Aortic dissection (AD) is a life-threatening condition. We developed an artificial intelligence (AI) algorithm capable of robust, accurate, and automated AD detection and sub-classification.
Materials and methods: Based on 2010-2023 data from Mannheim University Medical Centre, heterogeneous internal training cases with confirmed AD (n = 70) were manually segmented and, together with non-AD cases (n = 87), used for training of a convolutional neural network (CNN; U-Net architecture) configured using the nnU-Net framework. Internal test dataset was composed of 106 cases. The external test was performed on a public dataset: 100 AD cases from ImageTBAD, Guangdong Provincial People's Hospital, China, and 38 non-AD cases from the AVT dataset (multiple sources). Model performance was evaluated by area under the receiver operating characteristic curve (AUROC), area under the precision-recall curve (AUPRC), sensitivity, specificity, precision, and F1-score, and by investigating performance on different subsets of cases. Confidence intervals were determined using DeLong's method and bootstrapping.
Results: The best-performing algorithm achieved an AUROC of 98.7% (95% CI: 96.1-100.0%) and an AUPRC of 98.9% (96.0-100.0%) on the internal test dataset, 97.0% (94.7-99.3%) and 99.06% (98.0-99.7%) on the external test datasets, respectively. In the internal test dataset, of 15 unsuspected AD cases, 14 (93.3%) were successfully detected by the algorithm. On the external test dataset, sensitivity, specificity, precision, and F1-score were 92.0%, 100.0%, 100.0%, and 95.8%, respectively.
Conclusion: The developed AI pipeline highlighted the capability of optimized CNNs to reliably detect AD across heterogeneous multicenter datasets. The resulting tool will be made publicly available for further scientific evaluation.
Relevance statement: Artificial Intelligence demonstrated promising potential to detect AD on heterogeneous thoracic CT imaging data.
Key points: Early detection of aortic dissection (AD) is crucial for timely treatment. A modern convolutional neural network (CNN) achieved 93.5% sensitivity and 100.0% specificity for AD detection on multicenter, heterogeneous CT data. These results demonstrate the potential of streamlined, optimized CNNs for robust AD detection on CT, supporting fast clinical response.
{"title":"Automated AI detection of thoracic aortic dissection on CT imaging.","authors":"Tobias Norajitra, Michael A Baumgartner, Lucas R Cusumano, Jesus G Ulloa, Christian S Rizzo, Florian Haag, Alexander Hertel, Nils A Rathmann, Steffen J Diehl, Stefan O Schoenberg, Klaus H Maier-Hein, Johann S Rink","doi":"10.1186/s41747-025-00640-8","DOIUrl":"10.1186/s41747-025-00640-8","url":null,"abstract":"<p><strong>Background: </strong>Aortic dissection (AD) is a life-threatening condition. We developed an artificial intelligence (AI) algorithm capable of robust, accurate, and automated AD detection and sub-classification.</p><p><strong>Materials and methods: </strong>Based on 2010-2023 data from Mannheim University Medical Centre, heterogeneous internal training cases with confirmed AD (n = 70) were manually segmented and, together with non-AD cases (n = 87), used for training of a convolutional neural network (CNN; U-Net architecture) configured using the nnU-Net framework. Internal test dataset was composed of 106 cases. The external test was performed on a public dataset: 100 AD cases from ImageTBAD, Guangdong Provincial People's Hospital, China, and 38 non-AD cases from the AVT dataset (multiple sources). Model performance was evaluated by area under the receiver operating characteristic curve (AUROC), area under the precision-recall curve (AUPRC), sensitivity, specificity, precision, and F1-score, and by investigating performance on different subsets of cases. Confidence intervals were determined using DeLong's method and bootstrapping.</p><p><strong>Results: </strong>The best-performing algorithm achieved an AUROC of 98.7% (95% CI: 96.1-100.0%) and an AUPRC of 98.9% (96.0-100.0%) on the internal test dataset, 97.0% (94.7-99.3%) and 99.06% (98.0-99.7%) on the external test datasets, respectively. In the internal test dataset, of 15 unsuspected AD cases, 14 (93.3%) were successfully detected by the algorithm. On the external test dataset, sensitivity, specificity, precision, and F1-score were 92.0%, 100.0%, 100.0%, and 95.8%, respectively.</p><p><strong>Conclusion: </strong>The developed AI pipeline highlighted the capability of optimized CNNs to reliably detect AD across heterogeneous multicenter datasets. The resulting tool will be made publicly available for further scientific evaluation.</p><p><strong>Relevance statement: </strong>Artificial Intelligence demonstrated promising potential to detect AD on heterogeneous thoracic CT imaging data.</p><p><strong>Key points: </strong>Early detection of aortic dissection (AD) is crucial for timely treatment. A modern convolutional neural network (CNN) achieved 93.5% sensitivity and 100.0% specificity for AD detection on multicenter, heterogeneous CT data. These results demonstrate the potential of streamlined, optimized CNNs for robust AD detection on CT, supporting fast clinical response.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"102"},"PeriodicalIF":3.6,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12546231/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348988","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-08DOI: 10.1186/s41747-025-00627-5
Giulio Bagnacci, Armando Perrella, Nunzia Di Meglio, Vito Di Martino, Letizia Sansotta, Francesco Gentili, Susanna Guerrini, Silvia Ruggeri, Cristina Intrieri, Stefania Piccioni, Daniele Marrelli, Maria Antonietta Mazzei
Background: Computed tomography (CT) is widely used to diagnose peritoneal metastases (PM), with debated accuracy. Dual-energy CT (DECT) may improve accuracy, yet its diagnostic performance is still unknown. We explored the potential of DECT for PM detection and quantification.
Materials and methods: We retrospectively included patients undergoing staging DECT for cancers with a high risk of peritoneal involvement, followed by staging laparoscopy/laparotomy, which served as the reference standard. Nine readers with varying experience levels (three expert, three intermediate, and three inexpert) reviewed two sets of images, separated by ≥ 60 days, considering the presence/absence of PM, abdominal region(s) involved, and calculated the radiological peritoneal cancer index (PCI). The first set included contrast-enhanced delayed-DECT scans reconstructed as virtual 120-kVp images; the second set also included virtual monoenergetic, 40-keV images and iodine maps. Performance metrics, receiver operating characteristic (ROC) analysis, McNemar, DeLong, and Wilcoxon tests were applied.
Results: Twenty patients (mean age 64.2 years; 12 females) were included, 10 with PM. At per-patient analysis, the addition of monoenergetic 40-keV images and iodine maps slightly increased the performance and improved inter-reader agreement, with significant benefit for inexperienced readers only (p = 0.010). Per-region analysis demonstrated a significant advantage with an area under the ROC curve ranging from 0.709 to 0.766 (p < 0.001), confirmed for each reader group; in addition, the inter-reader agreement significantly improved. Quantitative analysis showed a reduction in the differences between CT results and surgical PCI by DECT (4 ± 12 versus 2 ± 9, p < 0.001).
Conclusion: DECT-derived reconstructions in the delayed-phase enhanced PM detection and quantification.
Relevance statement: Delayed-phase DECT reconstruction showed superior accuracy over conventional CT in detecting and quantifying peritoneal metastases. These findings could help establish a new standard CT protocol for malignancies with peritoneal tropism.
Key points: CT is the most widely used technique for assessing peritoneal metastases. The accuracy of CT for peritoneal metastases is debated; dual-energy CT shows promise. In our study, delayed-phase dual-energy CT provided significant advantages for all readers.
{"title":"Improved detection and quantification of peritoneal metastases using delayed contrast-enhanced dual-energy CT scans.","authors":"Giulio Bagnacci, Armando Perrella, Nunzia Di Meglio, Vito Di Martino, Letizia Sansotta, Francesco Gentili, Susanna Guerrini, Silvia Ruggeri, Cristina Intrieri, Stefania Piccioni, Daniele Marrelli, Maria Antonietta Mazzei","doi":"10.1186/s41747-025-00627-5","DOIUrl":"10.1186/s41747-025-00627-5","url":null,"abstract":"<p><strong>Background: </strong>Computed tomography (CT) is widely used to diagnose peritoneal metastases (PM), with debated accuracy. Dual-energy CT (DECT) may improve accuracy, yet its diagnostic performance is still unknown. We explored the potential of DECT for PM detection and quantification.</p><p><strong>Materials and methods: </strong>We retrospectively included patients undergoing staging DECT for cancers with a high risk of peritoneal involvement, followed by staging laparoscopy/laparotomy, which served as the reference standard. Nine readers with varying experience levels (three expert, three intermediate, and three inexpert) reviewed two sets of images, separated by ≥ 60 days, considering the presence/absence of PM, abdominal region(s) involved, and calculated the radiological peritoneal cancer index (PCI). The first set included contrast-enhanced delayed-DECT scans reconstructed as virtual 120-kVp images; the second set also included virtual monoenergetic, 40-keV images and iodine maps. Performance metrics, receiver operating characteristic (ROC) analysis, McNemar, DeLong, and Wilcoxon tests were applied.</p><p><strong>Results: </strong>Twenty patients (mean age 64.2 years; 12 females) were included, 10 with PM. At per-patient analysis, the addition of monoenergetic 40-keV images and iodine maps slightly increased the performance and improved inter-reader agreement, with significant benefit for inexperienced readers only (p = 0.010). Per-region analysis demonstrated a significant advantage with an area under the ROC curve ranging from 0.709 to 0.766 (p < 0.001), confirmed for each reader group; in addition, the inter-reader agreement significantly improved. Quantitative analysis showed a reduction in the differences between CT results and surgical PCI by DECT (4 ± 12 versus 2 ± 9, p < 0.001).</p><p><strong>Conclusion: </strong>DECT-derived reconstructions in the delayed-phase enhanced PM detection and quantification.</p><p><strong>Relevance statement: </strong>Delayed-phase DECT reconstruction showed superior accuracy over conventional CT in detecting and quantifying peritoneal metastases. These findings could help establish a new standard CT protocol for malignancies with peritoneal tropism.</p><p><strong>Key points: </strong>CT is the most widely used technique for assessing peritoneal metastases. The accuracy of CT for peritoneal metastases is debated; dual-energy CT shows promise. In our study, delayed-phase dual-energy CT provided significant advantages for all readers.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"9 1","pages":"101"},"PeriodicalIF":3.6,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12508340/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145253101","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}