治疗后 4 小时和 24 小时[177Lu]Lu-PSMA SPECT/CT 与治疗前 PSMA PET/CT 在评估转移性阉割耐药前列腺癌男性患者病情方面的比较。

Mina Swiha, Sarennya Pathmanandavel, Nathan Papa, Zahra Sabahi, Sherrington Li, Alex Zheng, Sobia Khan, Maria Ayers, Shikha Sharma, Megan Crumbaker, Andrew Nguyen, Lyn Chan, Narjess Ayati, Louise Emmett
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This study investigated 4-h [<sup>177</sup>Lu]Lu-PSMA SPECT/CT as an alternative to 24-h [<sup>177</sup>Lu]Lu-PSMA SPECT/CT for evaluation of treatment response. <b>Methods:</b> This prospective analysis enrolled 23 patients diagnosed with mCRPC commencing [<sup>177</sup>Lu]Lu-PSMA-I&T therapy. Two patients were excluded because of incomplete imaging data. Posttherapy SPECT/CT was performed at 4 and 24 h after the first dose and 4 h after the second dose. Baseline [<sup>68</sup>Ga]Ga-PSMA-11 PET/CT and 4- and 24-h [<sup>177</sup>Lu]Lu-PSMA SPECT/CT were analyzed both visually and semiquantitatively. Bland-Altman plots assessed agreement of semiquantitative parameters from the 4- and 24-h scans. Quantitative assessment of the change in the total tumor volume (TTV) on the 4-h [<sup>177</sup>Lu]Lu-PSMA SPECT/CT after the first and second doses was correlated to patient outcomes. <b>Results:</b> All patients had mCRPC previously treated with an androgen receptor pathway inhibitor, and 11 (52%) received prior taxane chemotherapy. Median age was 78 y, and median prostate-specific antigen level was 54 ng/mL. On visual analysis, disease distribution was unchanged among the 3 imaging methods. Eleven patients (52%) had a median of 1 lesion not identified on 4-h [<sup>177</sup>Lu]Lu-PSMA SPECT/CT compared with 24-h [<sup>177</sup>Lu]Lu-PSMA SPECT/CT. All missed lesions on the 4-h [<sup>177</sup>Lu]Lu SPECT/CT were smaller than 2 cm. Mean differences and agreement between 4- and 24-h SPECT/CT quantitative parameters were within acceptable bounds for lesion number, SUV<sub>max</sub>, and SUV<sub>mean</sub>, with higher variation observed for TTV. 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引用次数: 0

摘要

[177Lu]Lu-前列腺特异性膜抗原(PSMA)是治疗转移性去势抵抗性前列腺癌(mCRPC)的有效方法。注射[177Lu]Lu-PSMA后24小时的[177Lu]Lu-PSMA SPECT/CT显示了作为[177Lu]Lu-PSMA治疗反应生物标志物的潜力,但对患者来说并不方便。本研究探讨了 4 小时 [177Lu]Lu-PSMA SPECT/CT 作为 24 小时 [177Lu]Lu-PSMA SPECT/CT 的替代方法,用于评估治疗反应。方法:这项前瞻性分析共纳入了23名确诊为开始接受[177Lu]Lu-PSMA-I&T治疗的mCRPC患者。有两名患者因成像数据不完整而被排除在外。治疗后SPECT/CT分别在首次给药后4小时和24小时以及第二次给药后4小时进行。对基线[68Ga]Ga-PSMA-11 PET/CT以及4小时和24小时[177Lu]Lu-PSMA SPECT/CT进行了视觉和半定量分析。平原-阿尔特曼图评估了 4 小时和 24 小时扫描的半定量参数的一致性。对第一次和第二次用药后4小时[177Lu]Lu-PSMA SPECT/CT上肿瘤总体积(TTV)的变化进行定量评估,并将其与患者预后相关联。结果:所有患者都曾接受过雄激素受体通路抑制剂治疗,其中11人(52%)曾接受过紫杉类药物化疗。年龄中位数为78岁,前列腺特异性抗原水平中位数为54纳克/毫升。经目测分析,3种成像方法的疾病分布情况相同。与24小时[177Lu]Lu-PSMA SPECT/CT相比,11名患者(52%)在4小时[177Lu]Lu-PSMA SPECT/CT中平均有1个病灶未被发现。4 h [177Lu]Lu SPECT/CT 上所有漏检病灶均小于 2 厘米。在病灶数目、SUVmax和SUVmean方面,4小时和24小时SPECT/CT定量参数的平均差和一致性都在可接受的范围内,TTV的差异较大。剂量 1 和剂量 2 [177Lu]Lu-PSMA SPECT/CT 之间 TTV 的变化可预测前列腺特异性抗原无进展生存期。结论注射后4小时的[177Lu]Lu-PSMA SPECT/CT似乎有望替代24小时的[177Lu]Lu-PSMA SPECT/CT进行治疗反应评估,为患者带来更多便利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Posttherapy 4- and 24-Hour [177Lu]Lu-PSMA SPECT/CT and Pretherapy PSMA PET/CT in Assessment of Disease in Men with Metastatic Castration-Resistant Prostate Cancer.

[177Lu]Lu-prostate-specific membrane antigen (PSMA) is an effective treatment for metastatic castration-resistant prostate cancer (mCRPC). [177Lu]Lu-PSMA SPECT/CT 24 h after injection has shown potential as a response biomarker for [177Lu]Lu-PSMA therapy but is not convenient for patients. This study investigated 4-h [177Lu]Lu-PSMA SPECT/CT as an alternative to 24-h [177Lu]Lu-PSMA SPECT/CT for evaluation of treatment response. Methods: This prospective analysis enrolled 23 patients diagnosed with mCRPC commencing [177Lu]Lu-PSMA-I&T therapy. Two patients were excluded because of incomplete imaging data. Posttherapy SPECT/CT was performed at 4 and 24 h after the first dose and 4 h after the second dose. Baseline [68Ga]Ga-PSMA-11 PET/CT and 4- and 24-h [177Lu]Lu-PSMA SPECT/CT were analyzed both visually and semiquantitatively. Bland-Altman plots assessed agreement of semiquantitative parameters from the 4- and 24-h scans. Quantitative assessment of the change in the total tumor volume (TTV) on the 4-h [177Lu]Lu-PSMA SPECT/CT after the first and second doses was correlated to patient outcomes. Results: All patients had mCRPC previously treated with an androgen receptor pathway inhibitor, and 11 (52%) received prior taxane chemotherapy. Median age was 78 y, and median prostate-specific antigen level was 54 ng/mL. On visual analysis, disease distribution was unchanged among the 3 imaging methods. Eleven patients (52%) had a median of 1 lesion not identified on 4-h [177Lu]Lu-PSMA SPECT/CT compared with 24-h [177Lu]Lu-PSMA SPECT/CT. All missed lesions on the 4-h [177Lu]Lu SPECT/CT were smaller than 2 cm. Mean differences and agreement between 4- and 24-h SPECT/CT quantitative parameters were within acceptable bounds for lesion number, SUVmax, and SUVmean, with higher variation observed for TTV. The change in TTV between dose 1 and 2 [177Lu]Lu-PSMA SPECT/CT predicted prostate-specific antigen progression-free survival. Conclusion: [177Lu]Lu-PSMA SPECT/CT at 4 h after injection appears a promising alternative to 24-h [177Lu]Lu-PSMA SPECT/CT for treatment response assessment, with improved patient convenience.

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