Vishnu Murthy, Koichiro Kimura, Lela Theus, Andrew Nguyen, Ojaswita Lokre, Timothy Perk, Pan Thin, Kathleen Nguyen, Vinicius Ludwig, Lucia Chen, Andrei Gafita, Johannes Czernin, Jeremie Calais
{"title":"人工智能辅助PSMA PET对177Lu-PSMA治疗的mCRPC患者的预后价值:一项回顾性单中心研究","authors":"Vishnu Murthy, Koichiro Kimura, Lela Theus, Andrew Nguyen, Ojaswita Lokre, Timothy Perk, Pan Thin, Kathleen Nguyen, Vinicius Ludwig, Lucia Chen, Andrei Gafita, Johannes Czernin, Jeremie Calais","doi":"10.2967/jnumed.125.269971","DOIUrl":null,"url":null,"abstract":"<p>This study aimed to explore the prognostic value of the artificial intelligence–assisted lesion tracking applied to prostate-specific membrane antigen (PSMA) PET in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with PSMA radiopharmaceutical therapy. <strong>Methods:</strong> TRAQinform IQ was applied to baseline and end-of-treatment <sup>68</sup>Ga-PSMA-11 PET scans from 20 patients with mCRPC treated with <sup>177</sup>Lu-PSMA-617. Lesion response parameters and the TRAQinform Profile score—designed for early treatment response assessment—were generated. Survival analyses were performed. <strong>Results:</strong> A higher percentage of “new” lesions was associated with a shorter overall survival (OS) (hazard ratio, 1.03; <em>P</em> = 0.002), whereas a higher percentage of “disappeared” lesions was linked to improved OS (hazard ratio, 0.98; <em>P</em> = 0.028). Patients with a TRAQinform Profile score of 2.7 or greater had a shorter OS than those with a score of less than 2.7 (10.9 mo vs. 44.3 mo; <em>P</em> = 0.027). <strong>Conclusion:</strong> Artificial intelligence–assisted lesion-tracking analysis of PSMA PET is prognostic for OS in patients with mCRPC undergoing PSMA radiopharmaceutical therapy.</p>","PeriodicalId":22820,"journal":{"name":"The Journal of Nuclear Medicine","volume":"3 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prognostic Value of AI-Assisted Lesion Tracking on End-of-Treatment PSMA PET in mCRPC Patients Treated with 177Lu-PSMA: A Retrospective, Single-Center Study\",\"authors\":\"Vishnu Murthy, Koichiro Kimura, Lela Theus, Andrew Nguyen, Ojaswita Lokre, Timothy Perk, Pan Thin, Kathleen Nguyen, Vinicius Ludwig, Lucia Chen, Andrei Gafita, Johannes Czernin, Jeremie Calais\",\"doi\":\"10.2967/jnumed.125.269971\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This study aimed to explore the prognostic value of the artificial intelligence–assisted lesion tracking applied to prostate-specific membrane antigen (PSMA) PET in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with PSMA radiopharmaceutical therapy. <strong>Methods:</strong> TRAQinform IQ was applied to baseline and end-of-treatment <sup>68</sup>Ga-PSMA-11 PET scans from 20 patients with mCRPC treated with <sup>177</sup>Lu-PSMA-617. Lesion response parameters and the TRAQinform Profile score—designed for early treatment response assessment—were generated. Survival analyses were performed. <strong>Results:</strong> A higher percentage of “new” lesions was associated with a shorter overall survival (OS) (hazard ratio, 1.03; <em>P</em> = 0.002), whereas a higher percentage of “disappeared” lesions was linked to improved OS (hazard ratio, 0.98; <em>P</em> = 0.028). Patients with a TRAQinform Profile score of 2.7 or greater had a shorter OS than those with a score of less than 2.7 (10.9 mo vs. 44.3 mo; <em>P</em> = 0.027). <strong>Conclusion:</strong> Artificial intelligence–assisted lesion-tracking analysis of PSMA PET is prognostic for OS in patients with mCRPC undergoing PSMA radiopharmaceutical therapy.</p>\",\"PeriodicalId\":22820,\"journal\":{\"name\":\"The Journal of Nuclear Medicine\",\"volume\":\"3 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Nuclear Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2967/jnumed.125.269971\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Nuclear Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2967/jnumed.125.269971","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Prognostic Value of AI-Assisted Lesion Tracking on End-of-Treatment PSMA PET in mCRPC Patients Treated with 177Lu-PSMA: A Retrospective, Single-Center Study
This study aimed to explore the prognostic value of the artificial intelligence–assisted lesion tracking applied to prostate-specific membrane antigen (PSMA) PET in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with PSMA radiopharmaceutical therapy. Methods: TRAQinform IQ was applied to baseline and end-of-treatment 68Ga-PSMA-11 PET scans from 20 patients with mCRPC treated with 177Lu-PSMA-617. Lesion response parameters and the TRAQinform Profile score—designed for early treatment response assessment—were generated. Survival analyses were performed. Results: A higher percentage of “new” lesions was associated with a shorter overall survival (OS) (hazard ratio, 1.03; P = 0.002), whereas a higher percentage of “disappeared” lesions was linked to improved OS (hazard ratio, 0.98; P = 0.028). Patients with a TRAQinform Profile score of 2.7 or greater had a shorter OS than those with a score of less than 2.7 (10.9 mo vs. 44.3 mo; P = 0.027). Conclusion: Artificial intelligence–assisted lesion-tracking analysis of PSMA PET is prognostic for OS in patients with mCRPC undergoing PSMA radiopharmaceutical therapy.