Analysis of Molecular Imaging Biomarkers Derived from [18F]FDG PET/CT in mCRPC: Whole-Body Total Lesion Glycolysis (TLG) Predicts Overall Survival in Patients Undergoing [225Ac]Ac-PSMA-617-Augmented [177Lu]Lu-PSMA-617 Radioligand Therapy
<b>Background/Objectives:</b> The augmentation of [<sup>177</sup>Lu]Lu-PSMA-617 radioligand therapy by alpha emitting [<sup>225</sup>Ac]Ac-PSMA-617, known as the tandem therapy concept, is a promising escalating treatment option in advanced mCRPC. In this study, we evaluated the value of [<sup>18</sup>F]FDG PET/CT-derived molecular imaging biomarkers for predicting response and outcome to PSMA tandem RLT in <i>n</i> = 33 patients with insufficient response on [<sup>177</sup>Lu]Lu-PSMA-617 monotherapy. <b>Methods:</b> Six different molecular imaging parameters at baseline, i.e., before initiation of PSMA tandem RLT with respect to SUV<sub>max</sub>, SUV<sub>peak</sub>, SUV<sub>5</sub>, SUV<sub>mean</sub>, metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were tested for association with response and overall survival (OS). <b>Results:</b> After the initiation of augmentation, 24.2% of patients with a previously insufficient response experienced partial remission, and 39.4% experienced stable disease. The median OS was 7 months (95% CI: 4-11 months). None of the tested parameters were able to predict the response (all <i>p</i> > 0.529). In contrast, the [<sup>18</sup>F]FDG PET/CT-derived whole-body molecular imaging parameter TLG was significantly (<i>p</i> = 0.029) associated with OS of patients undergoing [<sup>225</sup>Ac]Ac-PSMA-617 augmented [<sup>177</sup>Lu]Lu-PSMA-617 RLT after insufficient response to [<sup>177</sup>Lu]Lu-PSMA-617 monotherapy. <b>Conclusion:</b> Implementing [<sup>18</sup>F]FDG PET/CT in the management of PSMA-RLT in clinical practice may contribute to outcome prediction and provide a route to more individualized management in mCRPC.
Authors
- Caroline Burgard (ORCID: https://orcid.org/0000-0003-1522-8860)
- Arne Blickle (ORCID: https://orcid.org/0009-0009-2460-7249)
- Fadi Khreish (ORCID: https://orcid.org/0000-0002-1036-7477)
- Samer Ezziddin (ORCID: https://orcid.org/0000-0003-4110-3375)
- Stephan Maus (ORCID: https://orcid.org/0000-0003-1679-8080)
- Sven Petto
- Mark Bartholomä (ORCID: https://orcid.org/0000-0002-0361-2833)
- Moritz B. Bastian
- Andrea Schaefer-Schuler (ORCID: https://orcid.org/0000-0002-2439-5786)
- Florian Rosar (ORCID: https://orcid.org/0000-0002-2985-4099)
- Tilman Speicher
- Lukas Dahlmanns
Institutions
- Saarland University (DE)
Publication Details
- Journal
- Cancers
- Published
- 2024-10-19
- DOI
- https://doi.org/10.3390/cancers16203532
- Citations
- 1
- Primary Topic
- Prostate Cancer Treatment and Research
- Type
- article
- Field-Weighted Citation Impact
- 0.42