99mTc-MIP-1404 SPECT/CT伴随诊断:177Lu-PSMA治疗转移性去势抵抗性前列腺癌

Thorsten Derlin, Liam Widjaja, Nina Natascha Harke, Christoph Czerner, Desiree Weiberg, Tobias L. Ross, Frank M. Bengel
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引用次数: 0

摘要

我们的目的是确定99mTc-MIP-1404 SPECT在接受基线分期和评估前列腺特异性膜抗原(PSMA)靶向放射药物治疗(RPT)转移性去势抵抗性前列腺癌患者中的可行性、诊断性能和预测价值。方法:回顾性分析46例接受99mTc-MIP-1404平面显像和SPECT/CT进行177Lu-PSMA RPT分期和资格评估的患者资料。评估整体图像质量,并对图像进行视觉分析,以确定病理性摄取的存在和定位。转移性摄取使用3分制进行视觉评分。99mTc-MIP-1404结果与随后开始RPT的患者的治疗后177Lu-PSMA扫描结果进行比较(n = 35)。评估99mTc-MIP-1404扫描摄取强度的预测和预后意义。结果:99mTc-MIP-1404扫描的图像质量98%为优。210个定位中的206个成像结果一致,与177u - psma扫描结果几乎完全一致(κ = 0.957 [95% CI, 0.916-0.999])。摄取强度高于肝摄取确定的应答者(P = 0.0115),并与延长无进展生存期相关(中位数,146天对96天;进展的风险比为0.3838 [95% CI, 0.1721-0.8556];P = 0.0192)。在多变量分析中,99mTc-MIP-1404摄取高于肝脏成为治疗反应的独立预测因子(优势比,12.37 [95% CI, 1.613-203.3];P = 0.0319)。然而,27%的应答者表现出不高于肝脏的摄取。结论:99mTc-MIP-1404影像适用于评估晚期转移性去势抵抗性前列腺癌患者的RPT资格。特别是,治疗前摄取强度可预测对177Lu-PSMA RPT的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
99mTc-MIP-1404 SPECT/CT Companion Diagnostic for 177Lu-PSMA Therapy in Metastatic Castration-Resistant Prostate Cancer

Our objective was to determine the feasibility, diagnostic performance, and predictive value of 99mTc-MIP-1404 SPECT in patients undergoing baseline staging and assessment of eligibility for prostate-specific membrane antigen (PSMA)–targeted radiopharmaceutical therapy (RPT) for metastatic castration-resistant prostate cancer. Methods: Data of 46 patients undergoing 99mTc-MIP-1404 planar scintigraphy and SPECT/CT for staging and assessment of eligibility for 177Lu-PSMA RPT were retrospectively analyzed. Overall image quality was assessed, and images were visually analyzed for the presence and localization of pathologic uptake. Metastatic uptake was visually scored using a 3-point scale. 99mTc-MIP-1404 findings were compared with the results of posttherapeutic 177Lu-PSMA scans in patients subsequently commencing RPT (n = 35). The predictive and prognostic significance of uptake intensity in 99mTc-MIP-1404 scans was evaluated. Results: The image quality of 99mTc-MIP-1404 scans was rated as excellent in 98% of cases. Imaging results were concordant in 206 of 210 localizations, demonstrating almost perfect agreement with 177Lu-PSMA scans (κ = 0.957 [95% CI, 0.916–0.999]). Uptake intensity higher than liver uptake identified responders (P = 0.0115) and was associated with prolonged progression-free survival (median, 146 vs. 96 d; hazard ratio for progression, 0.3838 [95% CI, 0.1721–0.8556]; P = 0.0192). In multivariable analysis, 99mTc-MIP-1404 uptake higher than in liver emerged as an independent predictor of treatment response (odds ratio, 12.37 [95% CI, 1.613–203.3]; P = 0.0319). Nevertheless, 27% of responders demonstrated uptake no higher than that in the liver. Conclusion: 99mTc-MIP-1404 imaging is suitable for assessment of eligibility for RPT in patients with advanced metastatic castration-resistant prostate cancer. In particular, pretherapeutic uptake intensity is predictive of response to 177Lu-PSMA RPT.

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