Comparison of Prostate-specific Membrane Antigen Reporting and Data System Version 1.0 versus 2.0 for Prostate Cancer Assessment.
IF 5.6
Q1 ONCOLOGY
Yassir Edrees Almalki, Mohammad Abd Alkhalik Basha, Susan Adil Ali, Ragab Hani Donkol, Maged Abdel Galil Hamed, Maha Ibrahim Metwally, Rania Mostafa A Hassan, Reem Abdel Fattah Frere, Amro Ahmed Esmat Abdul Rahman, Yasmin Ibrahim Libda, Nader E M Mahmoud, Mohamed Hesham Saleh Saleh Radwan, Ibrahim M Eladl, Amgad M Elsheikh, Mohamed M A Zaitoun, Al-Shaimaa Mohamed Mohamed, Ghada Adel AbdelHamid, Heba Fathy Tantawy, Shimaa Elsayed Badr, Walid Mosallam, Mohammad Al-Shatouri, Waleed S Abo Shanab, Tamer Mahmoud Dawoud, Hamada M Khater, Rasha Taha Abouelkheir, Heba Abdelhamed, Ahmed Ali Obaya, Basant Sh Elshafaay, Ahmed M Abdelkhalik Basha, Reem M Abdelkhalik Mohammad, Noha Yahia Ebaid
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{"title":"Comparison of Prostate-specific Membrane Antigen Reporting and Data System Version 1.0 versus 2.0 for Prostate Cancer Assessment.","authors":"Yassir Edrees Almalki, Mohammad Abd Alkhalik Basha, Susan Adil Ali, Ragab Hani Donkol, Maged Abdel Galil Hamed, Maha Ibrahim Metwally, Rania Mostafa A Hassan, Reem Abdel Fattah Frere, Amro Ahmed Esmat Abdul Rahman, Yasmin Ibrahim Libda, Nader E M Mahmoud, Mohamed Hesham Saleh Saleh Radwan, Ibrahim M Eladl, Amgad M Elsheikh, Mohamed M A Zaitoun, Al-Shaimaa Mohamed Mohamed, Ghada Adel AbdelHamid, Heba Fathy Tantawy, Shimaa Elsayed Badr, Walid Mosallam, Mohammad Al-Shatouri, Waleed S Abo Shanab, Tamer Mahmoud Dawoud, Hamada M Khater, Rasha Taha Abouelkheir, Heba Abdelhamed, Ahmed Ali Obaya, Basant Sh Elshafaay, Ahmed M Abdelkhalik Basha, Reem M Abdelkhalik Mohammad, Noha Yahia Ebaid","doi":"10.1148/rycan.240390","DOIUrl":null,"url":null,"abstract":"<p><p>Purpose To assess diagnostic performance and reliability of Prostate-specific Membrane Antigen Reporting and Data System (PSMA-RADS) version 1.0 in evaluating prostate cancer (PCa) and compare it with the updated version (version 2.0). Materials and Methods This prospective, multicenter study was conducted between June 2022 and August 2024. Participants with PCa underwent gallium 68 (<sup>68</sup>Ga) PSMA-11 PET/CT imaging and were divided into three groups: new diagnoses, biochemical recurrence (BCR), and follow-up. Three nuclear medicine radiologists independently interpreted the images using PSMA-RADS version 1.0, followed by a retrospective assessment using PSMA-RADS version 2.0. Diagnostic performance was calculated using linear mixed-model analysis. Histopathology and follow-up data served as reference standards. Interrater agreement was evaluated using the intraclass correlation coefficient (ICC). Results The study included 443 male participants (mean age, 68.6 years ± 8.1 [SD]) divided into new diagnoses (<i>n</i> = 164), BCR (<i>n</i> = 108), and follow-up (<i>n</i> = 171) groups. Compared with PSMA-RADS version 1.0, version 2.0 improved diagnostic accuracy in new diagnoses (95.9% vs 97.4%, <i>P</i> = .02), BCR (92.6% vs 95.7%, <i>P</i> = .004), and follow-up (88.7% vs 94.7%, <i>P</i> < .001). Sensitivity substantially improved in follow-up cases (87.7% vs 95.7%, <i>P</i> < .001). Interrater agreement was comparable between two versions, with lowest reliability in soft tissue evaluation (ICC = 0.36-0.50). Introduction of the PSMA-RADS 5T category to version 2.0 enhanced the characterization of treated metastases, improving correlation with prostate-specific antigen dynamics (<i>r</i><sub>s</sub> = 0.74 vs 0.61, <i>P</i> < .001) and the discrimination of treatment response (88.7% vs 82.3%, <i>P</i> = .02). Conclusion Both PSMA-RADS versions 1.0 and 2.0 were highly accurate and reliable for PCa imaging, with version 2.0 offering significant improvements, particularly in challenging follow-up and BCR cases. <b>Keywords:</b> PET/CT, Urinary, Prostate, Neoplasms-Primary, Oncology, Comparative Studies, Prostate Cancer, PSMA-RADS, Diagnostic Performance, Reliability Clinical trial registration no.: NCT06359717 <i>Supplemental material is available for this article.</i> © RSNA, 2025.</p>","PeriodicalId":20786,"journal":{"name":"Radiology. Imaging cancer","volume":"7 3","pages":"e240390"},"PeriodicalIF":5.6000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12130719/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology. Imaging cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1148/rycan.240390","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
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Abstract
Purpose To assess diagnostic performance and reliability of Prostate-specific Membrane Antigen Reporting and Data System (PSMA-RADS) version 1.0 in evaluating prostate cancer (PCa) and compare it with the updated version (version 2.0). Materials and Methods This prospective, multicenter study was conducted between June 2022 and August 2024. Participants with PCa underwent gallium 68 (68 Ga) PSMA-11 PET/CT imaging and were divided into three groups: new diagnoses, biochemical recurrence (BCR), and follow-up. Three nuclear medicine radiologists independently interpreted the images using PSMA-RADS version 1.0, followed by a retrospective assessment using PSMA-RADS version 2.0. Diagnostic performance was calculated using linear mixed-model analysis. Histopathology and follow-up data served as reference standards. Interrater agreement was evaluated using the intraclass correlation coefficient (ICC). Results The study included 443 male participants (mean age, 68.6 years ± 8.1 [SD]) divided into new diagnoses (n = 164), BCR (n = 108), and follow-up (n = 171) groups. Compared with PSMA-RADS version 1.0, version 2.0 improved diagnostic accuracy in new diagnoses (95.9% vs 97.4%, P = .02), BCR (92.6% vs 95.7%, P = .004), and follow-up (88.7% vs 94.7%, P < .001). Sensitivity substantially improved in follow-up cases (87.7% vs 95.7%, P < .001). Interrater agreement was comparable between two versions, with lowest reliability in soft tissue evaluation (ICC = 0.36-0.50). Introduction of the PSMA-RADS 5T category to version 2.0 enhanced the characterization of treated metastases, improving correlation with prostate-specific antigen dynamics (r s = 0.74 vs 0.61, P < .001) and the discrimination of treatment response (88.7% vs 82.3%, P = .02). Conclusion Both PSMA-RADS versions 1.0 and 2.0 were highly accurate and reliable for PCa imaging, with version 2.0 offering significant improvements, particularly in challenging follow-up and BCR cases. Keywords: PET/CT, Urinary, Prostate, Neoplasms-Primary, Oncology, Comparative Studies, Prostate Cancer, PSMA-RADS, Diagnostic Performance, Reliability Clinical trial registration no.: NCT06359717 Supplemental material is available for this article. © RSNA, 2025.
前列腺特异性膜抗原报告和数据系统1.0版与2.0版在前列腺癌评估中的比较。
目的评价前列腺特异性膜抗原报告与数据系统(PSMA-RADS) 1.0版对前列腺癌(PCa)的诊断效能和可靠性,并与更新后的PSMA-RADS 2.0版进行比较。材料与方法该前瞻性多中心研究于2022年6月至2024年8月进行。前列腺癌患者行68镓(68Ga) PSMA-11 PET/CT显像,并分为三组:新诊断组、生化复发组和随访组。三名核医学放射科医师使用PSMA-RADS 1.0版本独立解释图像,随后使用PSMA-RADS 2.0版本进行回顾性评估。诊断性能采用线性混合模型分析计算。组织病理学及随访资料作为参考标准。用类内相关系数(ICC)评价组间一致性。结果共纳入443例男性受试者(平均年龄68.6±8.1岁[SD]),分为新诊断组(n = 164)、BCR组(n = 108)和随访组(n = 171)。与PSMA-RADS 1.0版本相比,2.0版本提高了新诊断的诊断准确性(95.9% vs 97.4%, P = 0.02)、BCR (92.6% vs 95.7%, P = 0.004)和随访(88.7% vs 94.7%, P < 0.001)。随访患者的敏感性显著提高(87.7% vs 95.7%, P < 0.001)。两种版本之间的一致性相当,软组织评估的可靠性最低(ICC = 0.36-0.50)。在2.0版本中引入PSMA-RADS 5T分类,增强了治疗转移的表征,改善了与前列腺特异性抗原动力学的相关性(rs = 0.74 vs 0.61, P < 0.001)和治疗反应的区分(88.7% vs 82.3%, P = 0.02)。结论PSMA-RADS 1.0和2.0版本对PCa成像的准确性和可靠性都很高,2.0版本有显著的改进,特别是在具有挑战性的随访和BCR病例中。关键词:PET/CT,泌尿,前列腺,原发肿瘤,肿瘤学,比较研究,前列腺癌,PSMA-RADS,诊断性能,可靠性NCT06359717本文有补充材料。©rsna, 2025。
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