Your browser doesn't support javascript.
loading
PSMA- and GRPR-Targeted PET: Results from 50 Patients with Biochemically Recurrent Prostate Cancer.
Baratto, Lucia; Song, Hong; Duan, Heying; Hatami, Negin; Bagshaw, Hilary P; Buyyounouski, Mark; Hancock, Steven; Shah, Sumit; Srinivas, Sandy; Swift, Patrick; Moradi, Farshad; Davidzon, Guido; Iagaru, Andrei.
Afiliação
  • Baratto L; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California.
  • Song H; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California.
  • Duan H; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California.
  • Hatami N; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California.
  • Bagshaw HP; Department of Radiation Oncology, Stanford University, Stanford, California; and.
  • Buyyounouski M; Department of Radiation Oncology, Stanford University, Stanford, California; and.
  • Hancock S; Department of Radiation Oncology, Stanford University, Stanford, California; and.
  • Shah S; Department of Medicine, Division of Oncology, Stanford University, Stanford, California.
  • Srinivas S; Department of Medicine, Division of Oncology, Stanford University, Stanford, California.
  • Swift P; Department of Radiation Oncology, Stanford University, Stanford, California; and.
  • Moradi F; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California.
  • Davidzon G; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California.
  • Iagaru A; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, Stanford, California; aiagaru@stanford.edu.
J Nucl Med ; 62(11): 1545-1549, 2021 11.
Article em En | MEDLINE | ID: mdl-33674398
ABSTRACT
Novel radiopharmaceuticals for PET are being evaluated for the diagnosis of biochemical recurrence (BCR) of prostate cancer (PC). We compared the gastrin-releasing peptide receptor-targeting 68Ga-RM2 with the prostate-specific membrane antigen (PSMA)-targeting 68Ga-PSMA11 and 18F-DCFPyL.

Methods:

Fifty patients underwent both 68Ga-RM2 PET/MRI and 68Ga-PSMA11 (n = 23) or 18F-DCFPyL (n = 27) PET/CT at an interval ranging from 1 to 60 d (mean ± SD, 15.8 ± 17.7 d). SUVmax was collected for all lesions.

Results:

68Ga-RM2 PET was positive in 35 and negative in 15 of the 50 patients. 68Ga-PSMA11/18F-DCFPyL PET was positive in 37 and negative in 13 of the 50 patients. Both scans detected 70 lesions in 32 patients. Forty-three lesions in 18 patients were identified on only 1 scan 68Ga-RM2 detected 7 more lesions in 4 patients, whereas 68Ga-PSMA11/18F-DCFPyL detected 36 more lesions in 13 patients.

Conclusion:

68Ga-RM2 remains a valuable radiopharmaceutical even when compared with the more widely used 68Ga-PSMA11/18F-DCFPyL in the evaluation of BCR of PC. Larger studies are needed to verify that identifying patients for whom these 2 classes of radiopharmaceuticals are complementary may ultimately allow for personalized medicine.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata Limite: Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata Limite: Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article