Francesco Lanfranchi, Liliana Belgioia, Domenico Albano, Luca Triggiani, Flavia Linguanti, Luca Urso, Rosario Mazzola, Alessio Rizzo, Elisa D'Angelo, Francesco Dondi, Eneida Mataj, Gloria Pedersoli, Elisabetta Maria Abenavoli, Luca Vaggelli, Beatrice Detti, Naima Ortolan, Antonio Malorgio, Alessia Guarneri, Federico Garrou, Matilde Fiorini, Serena Grimaldi, Pietro Ghedini, Giuseppe Carlo Iorio, Antonella Iudicello, Guido Rovera, Giuseppe Fornarini, Diego Bongiovanni, Michela Marcenaro, Filippo Maria Pazienza, Giorgia Timon, Matteo Salgarello, Manuela Racca, Mirco Bartolomei, Stefano Panareo, Umberto Ricardi, Francesco Bertagna, Filippo Alongi, Salvina Barra, Silvia Morbelli, Gianmario Sambuceti, Matteo Bauckneht
Prospective trials suggest that metastasis-directed therapy (MDT) is an effective treatment for patients with oligometastatic prostate cancer (PCa). Gallium 68 (68Ga) prostate-specific membrane antigen (PSMA)-11 PET/CT-guided MDT seems to improve the oncologic outcome in these patients compared with fluorine 18 (18F)-fluorocholine and 18F-PSMA-1007 PET/CT-guided MDT, but the effects in terms of local or distant disease control remain unclear. Thus, the present subanalysis of the PRECISE-MDT study analyzed patients with hormone-sensitive PCa who underwent MDT guided by PET/CT for nodal or bone oligorecurrent disease and were restaged with the same imaging modality in case of biochemical recurrence after MDT. Among 340 lesions detected in 241 male patients (median age, 74 [IQR, 9] years), 18F-fluorocholine, 68Ga-PSMA-11, and 18F-PSMA-1007 PET/CT-guided MDT was performed in 179, 81, and 80 lesions, respectively. At restaging imaging, the PET/CT imaging modality used to guide MDT was not significantly associated with local recurrence-free survival (LRFS), with median LRFS not reached for 68Ga-PSMA-11 PET/CT, 18F-PSMA-11 PET/CT, and 18F-fluorocholine PET/CT (P = .73). However, the detection rate of a new metastasis was significantly higher if MDT was guided by 18F-fluorocholine PET/CT (119 of 179 lesions, 66.5%) compared with 68Ga-PSMA-11 or 18F-PSMA-1007 PET/CT (23 of 81 lesions, 28%, and 27 of 80, 34%, respectively; P < .001 for both). Moreover, MDT guided by 68Ga-PSMA-11 PET/CT led to an improved median metastasis-free survival (MFS) (not reached) compared with 18F-PSMA-1007 (median MFS, 24.9 months; P < .001) or 18F-fluorocholine PET/CT (median MFS, 18 months; P < .001). These findings suggest that using different PET/CT imaging modalities to guide MDT might impact the distant disease control in this clinical scenario. Keywords: Radiation Therapy, Oncology, Urinary, Prostate, PET/CT Supplemental material is available for this article. Published under a CC BY 4.0 license.
{"title":"Impact of Metastasis-directed Therapy Guided by Different PET/CT Radiotracers on Distant and Local Disease Control in Oligorecurrent Hormone-sensitive Prostate Cancer: A Secondary Analysis of the PRECISE-MDT Study.","authors":"Francesco Lanfranchi, Liliana Belgioia, Domenico Albano, Luca Triggiani, Flavia Linguanti, Luca Urso, Rosario Mazzola, Alessio Rizzo, Elisa D'Angelo, Francesco Dondi, Eneida Mataj, Gloria Pedersoli, Elisabetta Maria Abenavoli, Luca Vaggelli, Beatrice Detti, Naima Ortolan, Antonio Malorgio, Alessia Guarneri, Federico Garrou, Matilde Fiorini, Serena Grimaldi, Pietro Ghedini, Giuseppe Carlo Iorio, Antonella Iudicello, Guido Rovera, Giuseppe Fornarini, Diego Bongiovanni, Michela Marcenaro, Filippo Maria Pazienza, Giorgia Timon, Matteo Salgarello, Manuela Racca, Mirco Bartolomei, Stefano Panareo, Umberto Ricardi, Francesco Bertagna, Filippo Alongi, Salvina Barra, Silvia Morbelli, Gianmario Sambuceti, Matteo Bauckneht","doi":"10.1148/rycan.240150","DOIUrl":"10.1148/rycan.240150","url":null,"abstract":"<p><p>Prospective trials suggest that metastasis-directed therapy (MDT) is an effective treatment for patients with oligometastatic prostate cancer (PCa). Gallium 68 (<sup>68</sup>Ga) prostate-specific membrane antigen (PSMA)-11 PET/CT-guided MDT seems to improve the oncologic outcome in these patients compared with fluorine 18 (<sup>18</sup>F)-fluorocholine and <sup>18</sup>F-PSMA-1007 PET/CT-guided MDT, but the effects in terms of local or distant disease control remain unclear. Thus, the present subanalysis of the PRECISE-MDT study analyzed patients with hormone-sensitive PCa who underwent MDT guided by PET/CT for nodal or bone oligorecurrent disease and were restaged with the same imaging modality in case of biochemical recurrence after MDT. Among 340 lesions detected in 241 male patients (median age, 74 [IQR, 9] years), <sup>18</sup>F-fluorocholine, <sup>68</sup>Ga-PSMA-11, and <sup>18</sup>F-PSMA-1007 PET/CT-guided MDT was performed in 179, 81, and 80 lesions, respectively. At restaging imaging, the PET/CT imaging modality used to guide MDT was not significantly associated with local recurrence-free survival (LRFS), with median LRFS not reached for <sup>68</sup>Ga-PSMA-11 PET/CT, <sup>18</sup>F-PSMA-11 PET/CT, and <sup>18</sup>F-fluorocholine PET/CT (<i>P</i> = .73). However, the detection rate of a new metastasis was significantly higher if MDT was guided by <sup>18</sup>F-fluorocholine PET/CT (119 of 179 lesions, 66.5%) compared with <sup>68</sup>Ga-PSMA-11 or <sup>18</sup>F-PSMA-1007 PET/CT (23 of 81 lesions, 28%, and 27 of 80, 34%, respectively; <i>P</i> < .001 for both). Moreover, MDT guided by <sup>68</sup>Ga-PSMA-11 PET/CT led to an improved median metastasis-free survival (MFS) (not reached) compared with <sup>18</sup>F-PSMA-1007 (median MFS, 24.9 months; <i>P</i> < .001) or <sup>18</sup>F-fluorocholine PET/CT (median MFS, 18 months; <i>P</i> < .001). These findings suggest that using different PET/CT imaging modalities to guide MDT might impact the distant disease control in this clinical scenario. <b>Keywords:</b> Radiation Therapy, Oncology, Urinary, Prostate, PET/CT <i>Supplemental material is available for this article.</i> Published under a CC BY 4.0 license.</p>","PeriodicalId":20786,"journal":{"name":"Radiology. Imaging cancer","volume":"7 3","pages":"e240150"},"PeriodicalIF":5.6,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12130722/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144079877","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}
Iwan Paolucci, Jessica Albuquerque Marques Silva, Yuan-Mao Lin, Alexander Shieh, Anna Maria Ierardi, Gianpaolo Caraffiello, Carlo Gazzera, Kyle A Jones, Paolo Fonio, Reto Bale, Kristy K Brock, Marco Calandri, Bruno C Odisio
Renee Miller, Mark Battle, Kristen Wangerin, Daniel T Huff, Amy J Weisman, Song Chen, Timothy G Perk, Gary A Ulaner
Purpose To evaluate two automated tools for detecting lesions on fluorine 18 (18F) fluoroestradiol (FES) PET/CT images and assess concordance of 18F-FES PET/CT with standard diagnostic CT and/or 18F fluorodeoxyglucose (FDG) PET/CT in patients with breast cancer. Materials and Methods This retrospective analysis of a prospective study included participants with breast cancer who underwent 18F-FES PET/CT examinations (n = 52), 18F-FDG PET/CT examinations (n = 13 of 52), and diagnostic CT examinations (n = 37 of 52). A convolutional neural network was trained for lesion detection using manually contoured lesions. Concordance in lesions labeled by a nuclear medicine physician between 18F-FES and 18F-FDG PET/CT and between 18F-FES PET/CT and diagnostic CT was assessed using an automated software medical device. Lesion detection performance was evaluated using sensitivity and false positives per participant. Wilcoxon tests were used for statistical comparisons. Results The study included 52 participants. The lesion detection algorithm achieved a median sensitivity of 62% with 0 false positives per participant. Compared with sensitivity in overall lesion detection, the sensitivity was higher for detection of high-uptake lesions (maximum standardized uptake value > 1.5, P = .002) and similar for detection of large lesions (volume > 0.5 cm3, P = .15). The artificial intelligence (AI) lesion detection tool was combined with a standardized uptake value threshold to demonstrate a fully automated method of labeling patients as having FES-avid metastases. Additionally, automated concordance analysis showed that 17 of 25 participants (68%) had over half of the detected lesions across two modalities present on 18F-FES PET/CT images. Conclusion An AI model was trained to detect lesions on 18F-FES PET/CT images and an automated concordance tool measured heterogeneity between 18F-FES PET/CT and standard-of-care imaging. Keywords: Molecular Imaging-Cancer, Neural Networks, PET/CT, Breast, Computer Applications-General (Informatics), Segmentation, 18F-FES PET, Metastatic Breast Cancer, Lesion Detection, Artificial Intelligence, Lesion Matching Supplemental material is available for this article. Clinical Trials Identifier: NCT04883814 Published under a CC BY 4.0 license.
{"title":"Evaluating Automated Tools for Lesion Detection on <sup>18</sup>F Fluoroestradiol PET/CT Images and Assessment of Concordance with Standard-of-Care Imaging in Metastatic Breast Cancer.","authors":"Renee Miller, Mark Battle, Kristen Wangerin, Daniel T Huff, Amy J Weisman, Song Chen, Timothy G Perk, Gary A Ulaner","doi":"10.1148/rycan.240253","DOIUrl":"10.1148/rycan.240253","url":null,"abstract":"<p><p>Purpose To evaluate two automated tools for detecting lesions on fluorine 18 (<sup>18</sup>F) fluoroestradiol (FES) PET/CT images and assess concordance of <sup>18</sup>F-FES PET/CT with standard diagnostic CT and/or <sup>18</sup>F fluorodeoxyglucose (FDG) PET/CT in patients with breast cancer. Materials and Methods This retrospective analysis of a prospective study included participants with breast cancer who underwent <sup>18</sup>F-FES PET/CT examinations (<i>n</i> = 52), <sup>18</sup>F-FDG PET/CT examinations (<i>n</i> = 13 of 52), and diagnostic CT examinations (<i>n</i> = 37 of 52). A convolutional neural network was trained for lesion detection using manually contoured lesions. Concordance in lesions labeled by a nuclear medicine physician between <sup>18</sup>F-FES and <sup>18</sup>F-FDG PET/CT and between <sup>18</sup>F-FES PET/CT and diagnostic CT was assessed using an automated software medical device. Lesion detection performance was evaluated using sensitivity and false positives per participant. Wilcoxon tests were used for statistical comparisons. Results The study included 52 participants. The lesion detection algorithm achieved a median sensitivity of 62% with 0 false positives per participant. Compared with sensitivity in overall lesion detection, the sensitivity was higher for detection of high-uptake lesions (maximum standardized uptake value > 1.5, <i>P</i> = .002) and similar for detection of large lesions (volume > 0.5 cm<sup>3</sup>, <i>P</i> = .15). The artificial intelligence (AI) lesion detection tool was combined with a standardized uptake value threshold to demonstrate a fully automated method of labeling patients as having FES-avid metastases. Additionally, automated concordance analysis showed that 17 of 25 participants (68%) had over half of the detected lesions across two modalities present on <sup>18</sup>F-FES PET/CT images. Conclusion An AI model was trained to detect lesions on <sup>18</sup>F-FES PET/CT images and an automated concordance tool measured heterogeneity between <sup>18</sup>F-FES PET/CT and standard-of-care imaging. <b>Keywords:</b> Molecular Imaging-Cancer, Neural Networks, PET/CT, Breast, Computer Applications-General (Informatics), Segmentation, <sup>18</sup>F-FES PET, Metastatic Breast Cancer, Lesion Detection, Artificial Intelligence, Lesion Matching <i>Supplemental material is available for this article.</i> Clinical Trials Identifier: NCT04883814 Published under a CC BY 4.0 license.</p>","PeriodicalId":20786,"journal":{"name":"Radiology. Imaging cancer","volume":"7 3","pages":"e240253"},"PeriodicalIF":5.6,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12134609/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143994915","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}
Purpose To develop and validate a deep multitask network, MultiRecNet, for fully automatic prediction of disease-free survival (DFS) in patients with neoadjuvant chemoradiotherapy (nCRT)-treated locally advanced rectal cancer (LARC). Materials and Methods This retrospective study collected clinical information and baseline multimodal MRI (T2, apparent diffusion coefficient [ADC], Dapp, and Kapp) data from patients with LARC after nCRT at three centers between October 2011 and May 2019. Patients from centers 1 and 2 were divided into training, validation, and internal testing sets, while patients from center 3 served as the external testing set. MultiRecNet is capable of simultaneously performing segmentation, classification, and survival prediction tasks within a single framework. Multiple combinations of data from different clinical stages (pretreatment and postoperative) were input into MultiRecNet to generate different models and identify the model with optimal performance. Evaluation metrics included the Dice similarity coefficient (DSC), the area under the receiver operating characteristic curve (AUC), and the Harrell concordance index (C-index) for the segmentation, classification, and survival prediction tasks, respectively. Results The study included 445 patients: 261 in the training set (median age, 60 years [IQR, 53-67 years]; 172 male), 37 in the validation set (median age, 61 years [IQR, 55-68 years]; 30 male), 75 in the internal testing set (median age, 60 years [IQR, 51-67 years]; 45 male), and 72 in the external testing set (median age, 55 years [IQR, 49-61 years]; 38 male). In the internal testing set, the best model based on MultiRecNet (the All model, with T2-weighted imaging, ADC, Dapp, Kapp, pretreatment clinical indicators, and postoperative pathologic indicators) achieved a DSC of 0.72 for tumor segmentation, an AUC of 0.97 (95% CI: 0.92, >.99) for recurrence or metastasis classification at 3 years, and a C-index of 0.92 for DFS prediction. In the external testing set, the model continued to perform well for survival prediction (C-index = 0.81, P < .001). Conclusion The MultiRecNet-based model enabled prognostic prediction in a fully automated end-to-end manner in patients with LARC following nCRT. Keywords: MR-Imaging, Abdomen/GI, Rectum, Oncology Supplemental material is available for this article. Published under a CC BY 4.0 license.
目的:开发并验证深度多任务网络MultiRecNet,用于全自动预测新辅助放化疗(nCRT)治疗的局部晚期直肠癌(LARC)患者的无病生存期(DFS)。材料与方法本回顾性研究收集了2011年10月至2019年5月三个中心的LARC nCRT术后患者的临床信息和基线多模态MRI (T2、表观扩散系数[ADC]、Dapp和Kapp)数据。中心1和中心2的患者分为训练组、验证组和内部测试组,中心3的患者为外部测试组。MultiRecNet能够在一个框架内同时执行分割、分类和生存预测任务。将不同临床阶段(预处理和术后)的数据多次组合输入到MultiRecNet中,生成不同的模型,并识别性能最优的模型。评估指标包括Dice相似系数(DSC)、受试者工作特征曲线下面积(AUC)和Harrell一致性指数(C-index),分别用于分割、分类和生存预测任务。结果纳入445例患者:训练组261例(中位年龄60岁[IQR, 53-67岁];男性172例),验证组37例(中位年龄61岁[IQR, 55-68岁];男性30例),内测组75例(中位年龄60岁[IQR, 51-67岁];男性45例),外检组72例(中位年龄55岁[IQR, 49-61岁];38名男性)。在内部测试集中,基于MultiRecNet的最佳模型(All模型,包括t2加权成像、ADC、Dapp、Kapp、预处理临床指标和术后病理指标)在肿瘤分割方面的DSC为0.72,在3年复发或转移分类方面的AUC为0.97 (95% CI: 0.92, >.99),在预测DFS方面的c指数为0.92。在外部测试集中,该模型在生存预测方面继续表现良好(C-index = 0.81, P < .001)。结论基于multirecnet的模型能够以完全自动化的端到端方式预测nCRT后LARC患者的预后。关键词:磁共振成像,腹部/胃肠道,直肠,肿瘤学,本文有补充资料。在CC BY 4.0许可下发布。
{"title":"Predicting Recurrence in Locally Advanced Rectal Cancer Using Multitask Deep Learning and Multimodal MRI.","authors":"Zonglin Liu, Runqi Meng, Qiong Ma, Zhen Guan, Rong Li, Caixia Fu, Yanfen Cui, Yiqun Sun, Tong Tong, Dinggang Shen","doi":"10.1148/rycan.240359","DOIUrl":"10.1148/rycan.240359","url":null,"abstract":"<p><p>Purpose To develop and validate a deep multitask network, MultiRecNet, for fully automatic prediction of disease-free survival (DFS) in patients with neoadjuvant chemoradiotherapy (nCRT)-treated locally advanced rectal cancer (LARC). Materials and Methods This retrospective study collected clinical information and baseline multimodal MRI (T2, apparent diffusion coefficient [ADC], <i>D</i><sub>app</sub>, and <i>K</i><sub>app</sub>) data from patients with LARC after nCRT at three centers between October 2011 and May 2019. Patients from centers 1 and 2 were divided into training, validation, and internal testing sets, while patients from center 3 served as the external testing set. MultiRecNet is capable of simultaneously performing segmentation, classification, and survival prediction tasks within a single framework. Multiple combinations of data from different clinical stages (pretreatment and postoperative) were input into MultiRecNet to generate different models and identify the model with optimal performance. Evaluation metrics included the Dice similarity coefficient (DSC), the area under the receiver operating characteristic curve (AUC), and the Harrell concordance index (C-index) for the segmentation, classification, and survival prediction tasks, respectively. Results The study included 445 patients: 261 in the training set (median age, 60 years [IQR, 53-67 years]; 172 male), 37 in the validation set (median age, 61 years [IQR, 55-68 years]; 30 male), 75 in the internal testing set (median age, 60 years [IQR, 51-67 years]; 45 male), and 72 in the external testing set (median age, 55 years [IQR, 49-61 years]; 38 male). In the internal testing set, the best model based on MultiRecNet (the All model, with T2-weighted imaging, ADC, <i>D</i><sub>app</sub>, <i>K</i><sub>app</sub>, pretreatment clinical indicators, and postoperative pathologic indicators) achieved a DSC of 0.72 for tumor segmentation, an AUC of 0.97 (95% CI: 0.92, >.99) for recurrence or metastasis classification at 3 years, and a C-index of 0.92 for DFS prediction. In the external testing set, the model continued to perform well for survival prediction (C-index = 0.81, <i>P</i> < .001). Conclusion The MultiRecNet-based model enabled prognostic prediction in a fully automated end-to-end manner in patients with LARC following nCRT. <b>Keywords:</b> MR-Imaging, Abdomen/GI, Rectum, Oncology <i>Supplemental material is available for this article.</i> Published under a CC BY 4.0 license.</p>","PeriodicalId":20786,"journal":{"name":"Radiology. Imaging cancer","volume":"7 3","pages":"e240359"},"PeriodicalIF":5.6,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12130701/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144187840","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}
{"title":"Estimating the Lifetime Cancer Risk Associated with CT Imaging.","authors":"Saumya Gurbani, Meagan A Bechel","doi":"10.1148/rycan.259011","DOIUrl":"10.1148/rycan.259011","url":null,"abstract":"","PeriodicalId":20786,"journal":{"name":"Radiology. Imaging cancer","volume":"7 3","pages":"e259011"},"PeriodicalIF":5.6,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12130688/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144187836","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}