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Gastrin Releasing Peptide Receptors-targeted PET Diagnostics and Radionuclide Therapy for Prostate Cancer Management: Preclinical and Clinical Developments of the Past 5 Years.
Dalm, Simone; Duan, Heying; Iagaru, Andrei.
Afiliação
  • Dalm S; Department of Radiology and Nuclear Medicine, Erasmus MC, Dr. Molewaterplein 40, Rotterdam 3015 GD, The Netherlands.
  • Duan H; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, 300 Pasteur Drive, H2200, Stanford, CA 94305, USA.
  • Iagaru A; Department of Radiology, Division of Nuclear Medicine and Molecular Imaging, Stanford University, 300 Pasteur Drive, H2200, Stanford, CA 94305, USA. Electronic address: aiagaru@stanford.edu.
PET Clin ; 19(3): 401-415, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38644111
ABSTRACT
Each tumor has its own distinctive molecular identity. Treatment, therefore, should be tailored to this unique cancer phenotype. Theragnostics uses the same compound for targeted imaging and treatment, radiolabeled to an appropriate radionuclide, respectively. Gastrin-releasing peptide receptors (GRPRs) are overexpressed in prostate cancer, and radiolabeled GRPR antagonists have shown high diagnostic performance at staging and biochemical recurrence. Several GRPR-targeting theragnostic compounds have been developed preclinically. Their translation into clinics is underway with 4 clinical trials recruiting participants with GRPR-expressing tumors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Receptores da Bombesina / Compostos Radiofarmacêuticos / Tomografia por Emissão de Pósitrons Limite: Humans / Male Idioma: En Revista: PET Clin Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Receptores da Bombesina / Compostos Radiofarmacêuticos / Tomografia por Emissão de Pósitrons Limite: Humans / Male Idioma: En Revista: PET Clin Ano de publicação: 2024 Tipo de documento: Article