PET/CT imaging of prostate cancer in the era of small molecule prostate specific membrane antigen targeted tracers.


Journal

Hellenic journal of nuclear medicine
ISSN: 1790-5427
Titre abrégé: Hell J Nucl Med
Pays: Greece
ID NLM: 101257471

Informations de publication

Date de publication:
Historique:
received: 07 08 2020
accepted: 18 10 2020
pubmed: 12 12 2020
medline: 14 9 2021
entrez: 11 12 2020
Statut: ppublish

Résumé

Staging and restaging of prostate cancer is crucial for treatment planning and prognosis. Accurate localization is of high relevance for a tailor-made therapy and an early detection of unknown metastatic spread can lead to a survival benefit. Evidence based guidelines that are currently in use were established using data from conventional imaging (such as magnetic resonance imaging (MRI), computed tomography (CT) and bone scintigraphy). Prostate-specific membrane antigen (PSMA) positron emission tomography (PET) is rapidly evolving with promising results. However, up to now there is little consensus about the usefulness of this method, especially since different guidelines are "biased" depending on the association that shapes them. Firstly, little data exists on the staging of low risk tumors and probably PSMA PET/CT should be avoided in this setup for most patients. On the other hand, it has been recently proven that PSMA PET/CT can replace CT and bone scintigraphy (combined) in staging of advanced prostate cancer. Furthermore, the examination gained general acceptance through its excellent performance in biochemical recurrence, both for castration naïve and castration resistant tumors, and should be implemented where available. It is undisputed that PSMA PET/CT provides a more accurate picture of prostate cancer patients and can lead to both upstaging and downstaging, thus affecting therapeutic management. Though it is not clear yet if the more accurate staging will lead to better therapeutic decisions and improve patient outcomes, PSMA PET/CT appears as the next imaging standard for prostate cancer for the years to come.

Identifiants

pubmed: 33306762
pii: s002449912211
doi: 10.1967/s002449912211
doi:

Substances chimiques

Antigens, Surface 0
Radioactive Tracers 0
Small Molecule Libraries 0
FOLH1 protein, human EC 3.4.17.21
Glutamate Carboxypeptidase II EC 3.4.17.21

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

339-345

Auteurs

Alexis Vrachimis (A)

Department of Nuclear Medicine, German Oncology Center, University Hospital of the European University, Limassol, Cyprus, 1 Nikis Avenue, 4108 Agios Athanasios, Limassol, Cyprus. Alexis.Vrachimis@goc.com.cy.

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Classifications MeSH