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双示踪剂 PET/CT 的预后意义:PSMA 配体和 [F]FDG PET/CT 在接受 [Lu]PSMA 放射性配体治疗的患者中的应用。

Prognostic implications of dual tracer PET/CT: PSMA ligand and [F]FDG PET/CT in patients undergoing [Lu]PSMA radioligand therapy.

机构信息

Department of Nuclear Medicine, Faculty of Medicine, Medical Center-University of Freiburg, Freiburg, Germany.

Department of Urology and Paediatric Urology, University Hospital Würzburg, Würzburg, Germany.

出版信息

Eur J Nucl Med Mol Imaging. 2021 Jun;48(6):2024-2030. doi: 10.1007/s00259-020-05160-8. Epub 2020 Dec 18.

Abstract

BACKGROUND

Prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) with Lu-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]fluorodeoxyglucose (FDG) PET/CT for outcome prediction in patients undergoing RLT.

MATERIALS AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

前列腺特异性膜抗原(PSMA)靶向放射性配体治疗(RLT)联合 Lu 标记的 PSMA 配体在转移性去势抵抗性前列腺癌(mCRPC)的晚期疾病阶段取得了显著效果。然而,并非所有患者都能从中受益。不同的治疗反应可以用肿瘤进展和先前治疗次数引起的异质性来解释。PSMA 配体 PET/CT 可能会遗漏 PSMA 阴性病变,从而低估肿瘤负荷。相反,高 FDG 摄取也可能是肿瘤侵袭性的指标,因此是 RLT 反应和总生存期(OS)不良预后标志物。本分析的目的是研究 PSMA 配体 PET/CT 和 [F]氟脱氧葡萄糖(FDG)PET/CT 联合用于预测接受 RLT 的患者预后的价值。

材料和方法

这项双中心分析纳入了 54 例接受 RLT 前进行 FDG 和 PSMA 配体 PET/CT 成像的 mCRPC 患者。所有患者均进行 PSMA 配体和 FDG 摄取的视觉评估。将至少有一个 FDG 阳性但 PSMA 阴性(FDG+/PSMA-)病变的患者与没有任何 FDG+/PSMA-病变的患者进行比较。采用对数秩分析评估亚组之间 OS 的差异。

结果

中位 OS 为 11 ± 1.8 个月(95%CI 7.4-14.6)。在基线 PET/CT 上至少有一个 FDG+/PSMA-病变的患者(n=18)的 OS 显著降低(p<0.001),中位 OS 为 6.0±0.5 个月(95%CI:5.0-7.0 个月)。相比之下,没有任何 FDG+/PSMA-病变的患者(n=36)的中位 OS 为 16.0±2.5 个月(95%CI:11.2-20.8 个月)。

结论

在接受 RLT 的 mCRPC 患者中,FDG+/PSMA-病变是总生存期的负预测因子。然而,尚不确定是否应将 FDG+/PSMA-病变患者排除在 PSMA RLT 之外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98ea/8113196/851bcf453ddb/259_2020_5160_Fig1_HTML.jpg

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