Prognostic Value of Early Follow-Up PSMA PET/CT After 2 Cycles of [ <sup>177</sup> Lu]Lu-PSMA RPT in Patients with mCRPC: Comparison with PSA Dynamics
Prostate-specific membrane antigen (PSMA) PET/CT is recommended for response evaluation during [<sup>177</sup>Lu]Lu-PSMA radiopharmaceutical therapy (RPT) in patients with metastatic castration-resistant prostate cancer (mCRPC). Evidence supporting the predictive value of such a follow-up PSMA PET/CT relative to changes in prostate-specific antigen (PSA) monitoring is limited. <b>Methods:</b> This retrospective study evaluated 109 patients with mCRPC receiving [<sup>177</sup>Lu]Lu-PSMA RPT. Patients underwent [<sup>18</sup>F]F-PSMA-1007 PET/CT at baseline and after 2 cycles of RPT. We compared baseline and follow-up scans to assess relative changes in PSMA tumor volume (PSMA-TV), SUV<sub>mean</sub>, and total lesion PSMA (TL-PSMA, defined as PSMA-TV × SUV<sub>mean</sub>). PSA change was also defined as the change from baseline to follow-up after the second cycle. The prognostic performance of laboratory and image-based changes for overall survival (OS) were then tested using univariate Cox regression. We also performed Kaplan-Meier analysis, applying a 25% threshold for increases in PSA level and PET-based parameters. Finally, direct comparison of the predictive value was tested in multivariate Cox regression, applying the same cutoff. <b>Results:</b> Relative changes in volumetric PET-based parameters after 2 cycles of RPT correlated significantly with the change in PSA level (<i>P</i> ≤ 0.006 for each), validating the reliability of PET quantification of changes for response evaluation. In a univariate analysis, changes in PSMA-TV (<i>P</i> = 0.012) and TL-PSMA (<i>P</i> = 0.014) were predictive for OS, with PSA change providing comparable significance (<i>P</i> = 0.012). Applying the established 25% threshold for increase, TL-PSMA change best identified patients at risk for shorter OS (hazard ratio [HR], 2.298; <i>P</i> = 0.004), outperforming both PSA change (HR, 1.292; <i>P</i> = 0.369) and PSMA-TV change (HR, 1.798; <i>P</i> = 0.024). Further, TL-PSMA change emerged as the sole independent predictor of OS in multivariate analysis (<i>P</i> = 0.016). <b>Conclusion:</b> During RPT, relative changes in volumetric PET metrics from baseline to follow-up PSMA PET/CT demonstrated superior predictive value over PSA monitoring. These results highlight the clinical utility of repeat PSMA PET/CT in patients with mCRPC and indicate that follow-up scans during treatment should not be omitted.
Authors
- Steven P. Rowe (ORCID: https://orcid.org/0000-0003-2897-4694)
- Liam Widjaja (ORCID: https://orcid.org/0000-0002-0243-9338)
- Konrad Klimek
- Astrid Delker
- Mathias J. Zacherl
- Johannes Hornfeck
- Sophie C. Siegmund
- Franz J. Gildehaus
- Jozefina Casuscelli
- Rudolf A. Werner
- Nina-Sophie Schmidt-Hegemann
- Christian Stief
Institutions
- LMU Klinikum (DE)
- German Center for Infection Research (DE)
- Huawei German Research Center (DE)
- Ludwig-Maximilians-Universität München (DE)
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- Journal of Nuclear Medicine
- Published
- 2026-03-26
- DOI
- https://doi.org/10.2967/jnumed.125.271859
- Primary Topic
- Prostate Cancer Treatment and Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00