Normal-organ distribution of PSMA-targeting PET radiopharmaceutical 18F-flotufolastat: a post hoc analysis of the LIGHTHOUSE and SPOTLIGHT studies.

IF 2 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING American journal of nuclear medicine and molecular imaging Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.62347/INCG3525
Ross Penny, Benjamin Fongenie, Phillip Davis, James Sykes
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Abstract

Background: High-affinity radiohybrid PSMA-targeting radiopharmaceutical 18F-flotufolastat (18F-rhPSMA-7.3) is newly approved for diagnostic imaging of prostate cancer. Here, we conduct a post hoc analysis of two phase 3 studies to quantify 18F-flotufolastat uptake in a range of normal organs.

Methods: All 718 evaluable 18F-flotufolastat scans from LIGHTHOUSE and SPOTLIGHT were re-evaluated. Additionally, patients' medical records were reviewed and any patients with high tumor burden (PSA>20 ng/mL), altered biodistribution (e.g., chronic kidney disease), major anatomical changes to normal organs (e.g., nephrectomy), or any other history of cancer were excluded. A medical physicist defined volumes of interest over specific organs for evaluation of SUVmean and SUVpeak per PERCIST 1.0 criteria. Normally distributed data are reported as mean (SD) and non-normally distributed data as median (IQR). The co-efficient of variation (CoV; calculated as SD/mean for normally distributed data and IQR/median for non-normally distributed data) was used to quantify variability of SUV metrics.

Results: In total, scans from 546 patients (244 primary, 302 recurrent) were eligible for this analysis. All organs were considered to be normally distributed except for the bladder and spleen. In the liver, the mean SUVmean was 6.7 (SD 1.7), CoV 26%, while the bladder median SUVmean was 10.6 (IQR 11.9), CoV 112%. The mean SUVpeak in the liver was 8.2 (SD 2.1), CoV 26% and median SUVpeak in the bladder was 16.0 (IQR 18.5), CoV 116%.

Conclusions: Physiological 18F-flotufolastat uptake in normal organs was broadly consistent with other renally-cleared radiopharmaceuticals, which may have clinically significant implications when considering patient selection for radioligand therapy. Additionally, the bladder median SUVpeak for 18F-flotufolastat was lower than that previously reported for 68Ga-PSMA-11 and 18F-DCFPyL.

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PSMA 靶向 PET 放射性药物 18F-flotufolastat 的正常器官分布:对 LIGHTHOUSE 和 SPOTLIGHT 研究的事后分析。
背景:高亲和力放射性杂交PSMA靶向放射性药物18F-flotufolastat(18F-rhPSMA-7.3)新近被批准用于前列腺癌的诊断成像。在此,我们对两项 3 期研究进行了事后分析,以量化 18F-flotufolastat 在一系列正常器官中的摄取量:重新评估了 LIGHTHOUSE 和 SPOTLIGHT 两项研究中所有 718 个可评估的 18F 氟伏司特扫描结果。此外,还审查了患者的病历,排除了肿瘤负荷高(PSA>20 ng/mL)、生物分布改变(如慢性肾病)、正常器官发生重大解剖学改变(如肾切除术)或有其他癌症病史的患者。医学物理学家根据 PERCIST 1.0 标准定义了特定器官的感兴趣体积,以评估 SUVmean 和 SUVpeak。正态分布数据以平均值(SD)报告,非正态分布数据以中位数(IQR)报告。变异系数(CoV;正态分布数据以标度/均值计算,非正态分布数据以IQR/中位数计算)用于量化SUV指标的变异性:共有 546 名患者(244 名原发性患者,302 名复发性患者)的扫描结果符合分析条件。除膀胱和脾脏外,所有器官均被认为呈正态分布。肝脏的平均 SUVmean 值为 6.7(SD 1.7),CoV 26%,而膀胱的中位 SUVmean 值为 10.6(IQR 11.9),CoV 112%。肝脏的平均 SUV 峰值为 8.2(SD 2.1),CoV 26%,膀胱的中位 SUV 峰值为 16.0(IQR 18.5),CoV 116%:结论:正常器官对18F-氟托司他的生理摄取与其他经肾脏清除的放射性药物基本一致,这可能对考虑选择接受放射性配体治疗的患者具有重要的临床意义。此外,18F-氟唑司特的膀胱中位SUV峰值低于之前报道的68Ga-PSMA-11和18F-DCFPyL。
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来源期刊
American journal of nuclear medicine and molecular imaging
American journal of nuclear medicine and molecular imaging RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
自引率
4.00%
发文量
4
期刊介绍: The scope of AJNMMI encompasses all areas of molecular imaging, including but not limited to: positron emission tomography (PET), single-photon emission computed tomography (SPECT), molecular magnetic resonance imaging, magnetic resonance spectroscopy, optical bioluminescence, optical fluorescence, targeted ultrasound, photoacoustic imaging, etc. AJNMMI welcomes original and review articles on both clinical investigation and preclinical research. Occasionally, special topic issues, short communications, editorials, and invited perspectives will also be published. Manuscripts, including figures and tables, must be original and not under consideration by another journal.
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