Prognostic Value of [F]FDG PET Combined with [Ga]Ga-PSMA PET as Pretreatment Imaging in Patients with Metastatic Castration-Resistant Prostate Cancer Treated with [Lu]Lu-PSMA-617.

Fiche publication

Date publication

août 2026

Journal

Journal of nuclear medicine : official publication, Society of Nuclear Medicine

Auteurs

Membres identifiés du Cancéropôle Est :
Pr MARIE Pierre-Yves , Pr OLIVIER Pierre , Pr VERGER Antoine , Dr CLAUDIN Marine

Tous les auteurs :
Bekkhoucha A, Zaragori T, Olivier P, Claudin M, Marie PY, Kunsch J, Verger A, Raymond P, Heyer S, Imbert L, Boursier C

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/42595484

Résumé

Prostate-specific membrane antigen (PSMA)-targeted radiopharmaceutical therapy with [Lu]Lu-PSMA-617 has reshaped the management of metastatic castration-resistant prostate cancer (mCRPC). This study aimed to assess the added prognostic value of [F]FDG PET beyond [Ga]Ga-PSMA-11 PET as pretreatment imaging and to develop an overall survival (OS) nomogram for patients with mCRPC who were treated with [Lu]Lu-PSMA-617. From February 2022 to November 2023, all patients with mCRPC treated with at least 1 cycle of [Lu]Lu-PSMA-617 were analyzed. Baseline [Ga]Ga-PSMA-11 and [F]FDG PET parameters (SUV, SUV, total metabolic tumor volume [TMTV], and total lesion activity) were extracted for both tracers. OS was modeled using 2 hierarchical least absolute shrinkage and selection operator Cox models: clinical covariates plus [Ga]Ga-PSMA-11 PET (M-PSMA) and clinical covariates plus [Ga]Ga-PSMA-11 PET plus [F]FDG PET (M-PSMA + FDG). Model discrimination was assessed using the optimism-corrected Harrell concordance index (C-index), whereas model improvement was assessed with changes in the C-index. The study included 99 patients with mCRPC, and the median OS was 14 mo (95% CI, 11.7-18.2 mo). In M-PSMA, the [Ga]Ga-PSMA-11 PET SUV was the only significant imaging parameter (hazard ratio, 0.897; 95% CI, 0.852-0.945; < 0.001). The addition of TMTV [F]FDG PET in M-PSMA + FDG yielded a modest improvement in prognostic performance (ΔC-index, 0.010; 95% CI, -0.021 to 0.044) but a refined risk prediction for patients with a high TMTV [F]FDG burden. The final model was used to construct a nomogram for predicting 12-mo OS probability. Quantitative [Ga]Ga-PSMA-11 PET parameters provide strong prognostic stratification in patients with mCRPC who were treated with [Lu]Lu-PSMA-617. Tumor burden, as measured on [F]FDG PET, adds incremental prognostic information beyond [Ga]Ga-PSMA-11 PET, resulting in a modest improvement in risk prediction and potential refinement of prognosis in selected high-risk patients.