Prognostic value of [18F]FDG- and PSMA-PET in patients evaluated for [177Lu]Lu-PSMA therapy of mCRPC

被引:1
作者
Telli, Tugce [1 ,2 ,3 ,4 ]
Lopes, Leonor [5 ]
Karpinski, Madeleine [1 ,2 ,3 ,4 ]
Pabst, Kim M. [1 ,2 ,3 ,4 ]
Gruenwald, Viktor [2 ,3 ,4 ,6 ]
Shi, Kuangyu [5 ]
Hadaschik, Boris [2 ,3 ,4 ,6 ]
Kesch, Claudia [2 ,3 ,4 ,6 ]
Umutlu, Lale [2 ,3 ,7 ]
Herrmann, Ken [1 ,2 ,3 ,4 ]
Seifert, Robert [1 ,2 ,3 ,4 ,5 ]
Fendler, Wolfgang P. [1 ,2 ,3 ,4 ]
机构
[1] Univ Hosp Essen, Dept Nucl Med, Essen, Germany
[2] German Canc Consortium DKTK, Partner Site Partnership DKFZ, Essen, Germany
[3] Univ Hosp Essenaq, Essen, Germany
[4] West German Canc WTZ, Essen, Germany
[5] Univ Hosp Bern, Dept Nucl Med, Bern, Switzerland
[6] Univ Hosp Essen, Dept Urol, Essen, Germany
[7] Univ Hosp Essen, Dept Diag & Intervent Radiol & Neuroradiol, Essen, Germany
关键词
FDG; PSMA; Prognostics; Biomarkers; Prostate cancer; RESISTANT PROSTATE-CANCER; OUTCOMES; CLASSIFICATION; TOMOGRAPHY; EXPRESSION;
D O I
10.1007/s00259-025-07198-y
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
<bold>Background: </bold>Prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) with Lu-177-labeled PSMA ligands has achieved remarkable results in advanced disease stages of metastatic castration-resistant prostate cancer (mCRPC). However, not all patients benefit from this therapy. Different treatment responses could be explained by tumor heterogeneity triggered by progression and the number of prior treatments. PSMA-negative lesions can be missed on PSMA ligand PET/CT, which subsequently results in an underestimation of tumor burden. Conversely, high FDG uptake may also be an indicator of tumor aggressiveness and thus a poor prognostic marker for response to RLT and overall survival (OS). The aim of this analysis was to investigate the prognostic value of combined PSMA ligand PET/CT and [F-18]fluorodeoxyglucose (FDG) PET/CT for outcome prediction in patients undergoing RLT. <bold>Materials and methods: </bold>This bicentric analysis included 54 patients with mCRPC who underwent both FDG and PSMA ligand PET/CT imaging before RLT. In all patients, the pattern of PSMA ligand and FDG uptake was visually assessed. Patients with at least one FDG-positive, but PSMA-negative (FDG+/PSMA-) lesions were compared to patients without any FDG+/PSMA- lesions. A log-rank analysis was used to assess the difference in OS between subgroups. <bold>Results: </bold>Median OS was 11 +/- 1.8 months (95% CI 7.4-14.6). A significantly lower OS (p < 0.001) was found in patients with at least one FDG+/PSMA- lesion at baseline PET/CTs (n = 18) with a median OS of 6.0 +/- 0.5 months (95% CI: 5.0-7.0 months). In comparison, patients without any FDG+/PSMA- lesions (n = 36) had a median OS of 16.0 +/- 2.5 months (95% CI: 11.2-20.8 months). <bold>Conclusion: </bold>FDG+/PSMA- lesions are a negative predictor of overall survival in patients with mCRPC undergoing RLT. However, it remains to be determined if patients with FDG+/PSMA- lesions should be excluded from PSMA RLT.
引用
收藏
页码:3199 / 3210
页数:12
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