Enhancing PSMA-uptake with androgen deprivation therapy - a new way to detect prostate cancer metastases?


Journal

International braz j urol : official journal of the Brazilian Society of Urology
ISSN: 1677-6119
Titre abrégé: Int Braz J Urol
Pays: Brazil
ID NLM: 101158091

Informations de publication

Date de publication:
Historique:
received: 16 08 2018
accepted: 08 01 2019
pubmed: 23 3 2019
medline: 30 7 2019
entrez: 23 3 2019
Statut: ppublish

Résumé

68Ga-PSMA PET/CT imaging is a promising modality for the staging of recurrent prostate cancer (PCa). Current evidence suggests limited diagnostic value of the 68Ga-PSMA PET/CT in PSA-levels ≤0.3ng/mL. Experimental data have demonstrated na increase in PSMA-expression in PCa metastases by androgen deprivation in vitro. The aim of the current study was to investigate a possible enhancing effect of PSMA with low-dose androgen deprivation in patients with BCR and low PSA-levels. Five patients with PCa and BCR, following radical prostatectomy, underwent 68Ga-PSMA PET/CT. A consecutive 68Ga-PSMA PET/CT was performed 6 to 11 days after injection of 80mg of Degarelix (Firmagon®). We recorded PSA and testosterone serum-levels and changes of PSMA-uptake in 68Ga-PSMA PET/CT images. Median PSA prior 68Ga-PSMA PET/CT was 0.27ng/mL. All patients had a decrease in testosterone serum levels from median 2.95μg/l to 0.16μg/l following Degarelix injection. We observed an increase in the standardized uptake value (SUV) in PSMA-positive lymphogenous and osseous lesions in two patients following androgen deprivation. In another two patients, no PSMA positive signals were detected in either the fi rst or the second scan. Our preliminary results of this feasibility assessment indicate a possible enhancing effect of PSMA-imaging induced by low-dose ADT. Despite several limitations and the small number of patients, this could be a new approach to improve staging by 68Ga-PSMA PET/CT in PCa patients with BCR after primary therapy. Further prospective studies with larger number of patients are needed to validate our findings.

Identifiants

pubmed: 30901173
doi: 10.1590/S1677-5538.IBJU.2018.0305
pii: IBJU20180305
pmc: PMC6786102
doi:

Substances chimiques

Androgen Antagonists 0
Gallium Isotopes 0
Gallium Radioisotopes 0
Membrane Glycoproteins 0
Oligopeptides 0
Organometallic Compounds 0
Radiopharmaceuticals 0
acetyl-2-naphthylalanyl-3-chlorophenylalanyl-1-oxohexadecyl-seryl-4-aminophenylalanyl(hydroorotyl)-4-aminophenylalanyl(carbamoyl)-leucyl-ILys-prolyl-alaninamide 0
gallium 68 PSMA-11 0
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Evaluation Study Journal Article

Langues

eng

Pagination

459-467

Informations de copyright

Copyright® by the International Brazilian Journal of Urology.

Déclaration de conflit d'intérêts

None declared.

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Auteurs

Conrad Leitsmann (C)

Department of Urology, University Medical Center Goettingen, Goettingen, Germany.

Paul Thelen (P)

Department of Urology, University Medical Center Goettingen, Goettingen, Germany.

Marianne Schmid (M)

Department of Urology, University Medical Center Goettingen, Goettingen, Germany.

Johannes Meller (J)

Department of Nuclear Medicine, University Medical Center Goettingen, Goettingen, Germany.

Carsten-Oliver Sahlmann (CO)

Department of Nuclear Medicine, University Medical Center Goettingen, Goettingen, Germany.

Birgit Meller (B)

Department of Nuclear Medicine, University Medical Center Goettingen, Goettingen, Germany.

Lutz Trojan (L)

Department of Urology, University Medical Center Goettingen, Goettingen, Germany.

Arne Strauss (A)

Department of Urology, University Medical Center Goettingen, Goettingen, Germany.

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Classifications MeSH