Teragnosis en medicina nuclear

  1. José Luis Carreras Delgado 1
  2. Alba M. Blanes García 2
  3. Cristina G. Wakfie-Corieh 2
  4. María N. Cabrera Martín 2
  5. Aída Ortega Candil 2
  6. Cristina Rodríguez Rey 2
  1. 1 Real Academia Nacional de Medicina de España – Medicina Física; Hospital Clínico San Carlos de Madrid
  2. 2 Hospital Clínico San Carlos de Madrid
    info

    Hospital Clínico San Carlos de Madrid

    Madrid, España

    ROR https://ror.org/04d0ybj29

Zeitschrift:
Anales de la Real Academia Nacional de Medicina

ISSN: 0034-0634

Datum der Publikation: 2020

Nummer: 137

Seiten: 54-59

Art: Artikel

DOI: 10.32440/AR.2020.137.01.REV06 DIALNET GOOGLE SCHOLAR lock_openOpen Access editor

Andere Publikationen in: Anales de la Real Academia Nacional de Medicina

Zusammenfassung

Theranostics in Nuclear Medicine consists in using molecules linked to radioactive isotopes for the diagnosis and treatment of diseases. This modality has undergone rapid development during the last decades, supporting “targeted therapy” and “personalized medicine” thanks to the research of a wide range of molecular targets. Theranostics has been used for years in thyroid cancer and hyperthyroidism and is currently being implemented in other entities such as neuroendocrine tumors and prostate cancer. In neuroendocrine tumors, ligands capable of binding to some somatostatin receptors are labeled with 68Ga are used for diagnostic use in the initial assessment of these patients and with 177Lu for destruction of tumor cells in metastatic and inoperable patients. The 177Lu also has a low proportion of γ emission that allows biodistribution to be confirmed by scintigraphy/SPECT. In prostate cancer, PSMA (membrane-specific prostate antigen) which is an overexpressed transmembrane glycoprotein in prostate tumors is used as a theranostic target. For diagnosis, 68Ga-PSMA-11 is used and 177Lu-PSMA-617 is used for treatment, which triggers selective cell death of prostate tumor cells, indicated in metastatic patients and in progression despite other treatments. As for the novel Fibroblast Activation Protein (FAP) expressed in different tumor entities, the ligand used is derived from quinoleins that have FAP inhibitory activity, known as Fibroblast Activation Protein Inhibitor (FAPI), present in the stroma of various malignant neoplasms. For diagnostic use in metastatic tumors, 68Ga-FAPI-04 is being used with rapid tumor distribution and excellent image contrast. Although there is little therapeutic evidence it is a promising radiopharmaceutical due to its easy combination with therapeutic radionuclides

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