Journal
JOURNAL OF NUCLEAR MEDICINE
Volume 62, Issue 10, Pages 1457-1460Publisher
SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.120.258434
Keywords
prostate-specific membrane antigen; Ga-68-NGUL; Ga-68-PSMA-11; biodistribution
Funding
- National Research Foundation of Korea - Korean government (MSIT) [NRF-2020R1A2C2011428, NRF-2020M2D9A1093988]
- Korea Health Technology R&D Project through the Korea Health Industry Development Institute [HI18C1916, HI19C0339]
- Creative-Pioneering Researchers Program through Seoul National University
- Technology Innovation Program - Ministry of Trade, Industry, and Energy (Korea) [20001235]
- Korea Evaluation Institute of Industrial Technology (KEIT) [20001235] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- National Research Foundation of Korea [2020M2D9A1093988] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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Ga-68-NGUL demonstrated lower uptake in normal organs, rapid urinary clearance, similar performance in detecting PSMA-avid primary and metastatic lesions compared to Ga-68-PSMA-11, but a relatively lower tumor-to-background ratio.
Ga-68-NOTA Glu-Urea-Lys (NGUL) is a novel prostate-specific membrane antigen (PSMA)-targeting tracer used for PET/CT imaging. This study aimed to compare performance in the detection of primary and metastatic lesions and to compare biodistribution between Ga-68-NGUL and Ga-68-PSMA-11 in the same patients with prostate cancer. Methods: Eleven patients with metastatic prostate cancer were prospectively recruited. The quantitative tracer uptake was determined in normal organs and in primary and metastatic lesions. Results: Ga-68-NGUL showed significantly lower normal-organ uptake and rapid urinary clearance. The number and sites of detected PSMA-positive primary and metastatic lesions were identical, and no significant quantitative uptake difference was observed. Ga-68-NGUL showed a relatively lower tumor-to-background ratio than Ga-68-PSMA-11. Conclusion: In a head-to-head comparison with Ga-68-PSMA-11, Ga-68-NGUL showed lower uptake in normal organs and similar performance in detecting PSMA-avid primary and metastatic lesions. Ga-68-NGUL could be a valuable option for PSMA imaging.
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