通过连续高速全身360°镉锌碲化SPECT综合分析转移性前列腺肿瘤前后变化[177Lu]Lu-PSMA治疗注射的预后价值。

IF 9.1
Julien Kunsch, Timothée Zaragori, Pierre Olivier, Marine Claudin, Pierre-Yves Marie, Perrine Raymond, Sébastien Heyer, Antoine Verger, Laetitia Imbert, Caroline Boursier
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This study assesses the prognostic information from a comprehensive analysis of tumor changes from the first to the last [<sup>177</sup>Lu]Lu-PSMA therapy injections, as provided by whole-body [<sup>177</sup>Lu]Lu SPECT recordings from a high-speed 360° cadmium-zinc-telluride (CZT) camera of mCRPC patients. <b>Methods:</b> We included mCRPC patients treated by [<sup>177</sup>Lu]Lu-PSMA-617 injections who underwent [<sup>68</sup>Ga]Ga-PSMA-11 PET before treatment, whole-body 360° [<sup>177</sup>Lu]Lu CZT SPECT recordings of only 18 min obtained 24 h after each [<sup>177</sup>Lu]Lu-PSMA therapy injection, and plasma prostate-specific antigen (PSA) measurements before each injection. We used Cox proportional hazards models to predict overall survival (OS) according to PSA evolution during treatment, as well as tumor SUV<sub>max</sub>, SUV<sub>mean</sub>, total uptake volume, and total lesion activity (TLA; total uptake volume × SUV<sub>mean</sub>) extracted from [<sup>68</sup>Ga]Ga-PSMA-11 PET and the first and last [<sup>177</sup>Lu]Lu SPECT scans. <b>Results:</b> We included 72 patients with a median age of 71 y (interquartile range, 64-77 y), treated with up to 6 [<sup>177</sup>Lu]Lu-PSMA injections. Among 57 patients with at least 2 [<sup>177</sup>Lu]Lu-PSMA treatment cycles, 35 (61%) died during a follow-up of 12.0 mo (range, 4.9-17.5 mo) from the last [<sup>177</sup>Lu]Lu-PSMA injection. Most PSA, PET, and SPECT variables were significant univariate predictors of OS. However, only 2 [<sup>177</sup>Lu]Lu SPECT variables were selected as multivariate predictors: SPECT detection of new bone lesions during treatment (<i>P</i> < 0.0001) and final SPECT TLA (<i>P</i> = 0.0007). 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引用次数: 0

摘要

[177Lu] lu -前列腺特异性膜抗原(PSMA)治疗的愤怒SPECT监测为转移性去势抵抗性前列腺癌(mCRPC)患者提供了重要的预后信息,但记录时间为36至90分钟,身体部分覆盖。本研究通过对mCRPC患者的高速360°镉锌碲化(CZT)相机的全身[177Lu]Lu SPECT记录,从第一次到最后一次[177Lu]Lu- psma治疗注射的肿瘤变化进行综合分析,评估预后信息。方法:我们纳入了接受[177Lu]Lu- psma -617注射治疗的mCRPC患者,在治疗前接受[68Ga]Ga-PSMA-11 PET,在每次注射[177Lu]Lu- psma治疗后24小时获得仅18分钟的全身360°[177Lu]Lu CZT SPECT记录,并在每次注射前测量血浆前列腺特异性抗原(PSA)。我们使用Cox比例风险模型,根据治疗期间PSA的演变,以及从[68Ga]Ga-PSMA-11 PET和第一次和最后一次[177Lu]Lu SPECT扫描中提取的肿瘤SUVmax、SUVmean、总摄取体积和总病变活性(TLA;总摄取体积× SUVmean)预测总生存期(OS)。结果:我们纳入了72例患者,中位年龄为71岁(四分位数范围为64-77岁),接受多达6次[177Lu]Lu-PSMA注射治疗。在57例至少接受2个[177Lu]Lu-PSMA治疗周期的患者中,35例(61%)在最后一次注射[177Lu]Lu-PSMA后的12.0个月(范围4.9-17.5个月)随访期间死亡。大多数PSA、PET和SPECT变量是OS的显著单变量预测因子。然而,只有2 [177Lu]Lu SPECT变量被选择作为多变量预测因子:SPECT检测治疗期间新骨病变(P < 0.0001)和最终SPECT TLA (P = 0.0007)。19例无新骨病变且最终TLA低于750 mL·SUV中位数的患者的平均生存时间为19.7个月(95% CI, 16.6-22.8个月),19例仅符合这两个标准中的一个的患者的平均生存时间为14.4个月(95% CI, 10.9-18.0个月),19例没有任何标准的患者的平均生存时间为6.9个月(95% CI, 4.5-9.6个月)。结论:从第一次到最后一次注射[177Lu]Lu- psma获得的肿瘤变化的综合分析,通过快速全身360°[177Lu]Lu CZT SPECT记录,为mCRPC患者提供了强有力的预后信息,优于治疗前传统的OS预测指标,如PSA演变和[68Ga]Ga-PSMA-11 PET变量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Value of Comprehensive Analysis of Metastatic Prostate Tumor Changes from First to Last [177Lu]Lu-PSMA Therapy Injections Through Serial High-Speed Whole-Body 360° Cadmium-Zinc-Telluride SPECT.

Anger SPECT monitoring of [177Lu]Lu-prostate-specific membrane antigen (PSMA) therapy provides significant prognostic information about patients with metastatic castration-resistant prostate cancer (mCRPC) but with 36- to 90-min recording times and partial body coverage. This study assesses the prognostic information from a comprehensive analysis of tumor changes from the first to the last [177Lu]Lu-PSMA therapy injections, as provided by whole-body [177Lu]Lu SPECT recordings from a high-speed 360° cadmium-zinc-telluride (CZT) camera of mCRPC patients. Methods: We included mCRPC patients treated by [177Lu]Lu-PSMA-617 injections who underwent [68Ga]Ga-PSMA-11 PET before treatment, whole-body 360° [177Lu]Lu CZT SPECT recordings of only 18 min obtained 24 h after each [177Lu]Lu-PSMA therapy injection, and plasma prostate-specific antigen (PSA) measurements before each injection. We used Cox proportional hazards models to predict overall survival (OS) according to PSA evolution during treatment, as well as tumor SUVmax, SUVmean, total uptake volume, and total lesion activity (TLA; total uptake volume × SUVmean) extracted from [68Ga]Ga-PSMA-11 PET and the first and last [177Lu]Lu SPECT scans. Results: We included 72 patients with a median age of 71 y (interquartile range, 64-77 y), treated with up to 6 [177Lu]Lu-PSMA injections. Among 57 patients with at least 2 [177Lu]Lu-PSMA treatment cycles, 35 (61%) died during a follow-up of 12.0 mo (range, 4.9-17.5 mo) from the last [177Lu]Lu-PSMA injection. Most PSA, PET, and SPECT variables were significant univariate predictors of OS. However, only 2 [177Lu]Lu SPECT variables were selected as multivariate predictors: SPECT detection of new bone lesions during treatment (P < 0.0001) and final SPECT TLA (P = 0.0007). Means of survival times were 19.7 mo (95% CI, 16.6-22.8 mo) in the 19 patients who showed no new bone lesions and final TLA lower than the median of 750 mL·SUV, 14.4 mo (95% CI, 10.9-18.0 mo) in the 19 patients with only 1 of these 2 criteria, and 6.9 mo (95% CI, 4.5-9.6 mo) in the 19 patients with neither criterion. Conclusion: A comprehensive analysis of tumor changes from the first to the last [177Lu]Lu-PSMA injections, obtained with fast whole-body 360° [177Lu]Lu CZT SPECT recordings, provides strong prognostic information about mCRPC patients, outperforming conventional OS predictors such as PSA evolution and [68Ga]Ga-PSMA-11 PET variables before treatment.

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