Preoperative PSMA-PET/CT as a predictor of biochemical persistence and early recurrence following radical prostatectomy with lymph node dissection.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
03 2022
Historique:
received: 11 05 2021
accepted: 20 08 2021
revised: 19 08 2021
pubmed: 3 9 2021
medline: 22 4 2022
entrez: 2 9 2021
Statut: ppublish

Résumé

This study aims to evaluate the predictive value of lymph nodes (LN) suspicious for metastases on preoperative prostate-specific membrane antigen (PSMA) PET/CT for biochemical persistence (BCP) and early biochemical recurrence (BCR) following robotic-assisted radical prostatectomy (RARP) with extended pelvic LN dissection (ePLND). We evaluated 213 patients with intermediate and high-risk prostate cancer (PCa) who underwent clinical staging with preoperative Forty patients (19%) were PSMA+. The overall incidence of pN1 was 23%. Sensitivity, specificity, PPV and NPV on a per patient level for the detection of pN1 was 29%, 84%, 35%, and 80% respectively. BCP was observed in 26 of 211 patients (12%) and early BCR in 23 of 110 patients (21%). The presence of PSMA+ was a significant predictor for BCP (OR 7.1, 2.9-17.1 95% CI) and BCR (OR 8.1, 2.9-22.6 95% CI). Preoperative PSMA-PET/CT may be a valuable tool for patient counseling for RARP and ePLND as it is a significant predictor for the risk of postoperative BCP and early BCR. We conclude that an ePLND should not be avoided in men with intermediate or high-risk PCa and preoperative negative PSMA-PET/CT, as 20% have microscopic LN metastasis.

Sections du résumé

BACKGROUND
This study aims to evaluate the predictive value of lymph nodes (LN) suspicious for metastases on preoperative prostate-specific membrane antigen (PSMA) PET/CT for biochemical persistence (BCP) and early biochemical recurrence (BCR) following robotic-assisted radical prostatectomy (RARP) with extended pelvic LN dissection (ePLND).
METHODS
We evaluated 213 patients with intermediate and high-risk prostate cancer (PCa) who underwent clinical staging with preoperative
RESULTS
Forty patients (19%) were PSMA+. The overall incidence of pN1 was 23%. Sensitivity, specificity, PPV and NPV on a per patient level for the detection of pN1 was 29%, 84%, 35%, and 80% respectively. BCP was observed in 26 of 211 patients (12%) and early BCR in 23 of 110 patients (21%). The presence of PSMA+ was a significant predictor for BCP (OR 7.1, 2.9-17.1 95% CI) and BCR (OR 8.1, 2.9-22.6 95% CI).
CONCLUSION
Preoperative PSMA-PET/CT may be a valuable tool for patient counseling for RARP and ePLND as it is a significant predictor for the risk of postoperative BCP and early BCR. We conclude that an ePLND should not be avoided in men with intermediate or high-risk PCa and preoperative negative PSMA-PET/CT, as 20% have microscopic LN metastasis.

Identifiants

pubmed: 34471231
doi: 10.1038/s41391-021-00452-y
pii: 10.1038/s41391-021-00452-y
doi:

Substances chimiques

Gallium Radioisotopes 0
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

65-70

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

Références

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Auteurs

D J H Baas (DJH)

Department of Urology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands. d.baas@cwz.nl.
Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands. d.baas@cwz.nl.

M Schilham (M)

Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.
Department of Medical Imaging, Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

R Hermsen (R)

Department of Nuclear Medicine, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.

J M S de Baaij (JMS)

Department of Urology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.

H J E J Vrijhof (HJEJ)

Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.
Department of Urology, Catharina Hospital, Eindhoven, The Netherlands.

R J Hoekstra (RJ)

Department of Urology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.
Department of Urology, Catharina Hospital, Eindhoven, The Netherlands.

J P M Sedelaar (JPM)

Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.
Department of Urology, Radboudumc, Nijmegen, The Netherlands.

H V N Küsters-Vandevelde (HVN)

Department of Pathology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.

M Gotthardt (M)

Department of Medical Imaging, Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

C H W Wijers (CHW)

CWZ Academy, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.

J P van Basten (JP)

Department of Urology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.

D M Somford (DM)

Department of Urology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
Prosper Prostate Cancer Clinics, Nijmegen/Eindhoven, The Netherlands.

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