Karimzadeh Amir, Hansen Kimberley, Hein Stefan, Haller Bernhard, Heck Matthias M, Tauber Robert, D Alessandria Calogero, Eiber Matthias, Rauscher Isabel
Department of Nuclear Medicine, School of Medicine and Health, TUM University Hospital, Munich, Germany.
Department of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
Eur J Nucl Med Mol Imaging. 2025 May 19. doi: 10.1007/s00259-025-07200-7.
This retrospective analysis evaluated the prognostic value of baseline F-flotufolastat-PET bone tumor metrics for severe hematologic toxicity in metastatic castration-resistant prostate cancer (mCRPC) patients treated with [Lu]Lu-PSMA-I&T.
Data from 182 mCRPC patients with baseline F-flotufolastat-PET scans and complete hematologic profiles were analyzed. Bone lesions were semiautomatically delineated, and clinical parameters (e.g., pretreatments, lab results) were assessed. Hematologic adverse events (AEs) were defined per Common Terminology Criteria for Adverse Events version 5.0, with grades 3-4 considered severe. Cox regression was used to identify prognostic factors for AEs.
Baseline bone tumor volume prognosticated leukocytopenia (HR 1.03 per 100 ml, p = 0.036), while the number of bone lesions was prognostic for anemia (HR 1.04 per 10 lesions, p < 0.001) and severe anemia (HR per 10 lesions 1.05, p = 0.009). Higher baseline hemoglobin correlated with reduced leukocytopenia (HR 0.74, p = 0.002), thrombocytopenia (HR 0.80, p = 0.033), and severe anemia (HR 0.52, p < 0.001). Baseline kidney dysfunction was linked to anemia (HR 2.46, p = 0.002) and severe anemia (HR 3.81, p = 0.023). Prior [Ra]Radiumdichloride treatment prognosticated severe thrombocytopenia (HR 6.43, p = 0.021).
Baseline F-flotufolastat-PET metrics and pretherapeutic clinical parameters are key prognostic factors for severe hematologic toxicity in mCRPC patients treated with [Lu]Lu-PSMA-I&T.
本回顾性分析评估了基线F-氟托泊司他-PET骨肿瘤指标对接受[镥]镥-PSMA-I&T治疗的转移性去势抵抗性前列腺癌(mCRPC)患者严重血液学毒性的预后价值。
分析了182例具有基线F-氟托泊司他-PET扫描和完整血液学资料的mCRPC患者的数据。对骨病变进行半自动勾画,并评估临床参数(如预处理、实验室结果)。根据《不良事件通用术语标准》第5.0版定义血液学不良事件(AE),3-4级被视为严重。采用Cox回归确定AE的预后因素。
基线骨肿瘤体积可预测白细胞减少(每100 ml的风险比为1.03,p = 0.036),而骨病变数量可预测贫血(每10个病变的风险比为1.04,p < 0.001)和严重贫血(每10个病变的风险比为1.05,p = 0.009)。较高的基线血红蛋白与白细胞减少(风险比为0.74,p = 0.002)、血小板减少(风险比为0.80,p = 0.033)和严重贫血(风险比为0.52,p < 0.001)的减少相关。基线肾功能不全与贫血(风险比为2.46,p = 0.002)和严重贫血(风险比为3.81,p = 0.023)有关。既往[镭]二氯化镭治疗可预测严重血小板减少(风险比为6.43,p = 0.021)。
基线F-氟托泊司他-PET指标和治疗前临床参数是接受[镥]镥-PSMA-I&T治疗的mCRPC患者严重血液学毒性的关键预后因素。