Lymph Node Assessment in Prostate Cancer: Evaluation of Iodine Quantification With Spectral Detector CT in Correlation to PSMA PET/CT.


Journal

Clinical nuclear medicine
ISSN: 1536-0229
Titre abrégé: Clin Nucl Med
Pays: United States
ID NLM: 7611109

Informations de publication

Date de publication:
01 04 2021
Historique:
pubmed: 15 1 2021
medline: 7 4 2021
entrez: 14 1 2021
Statut: ppublish

Résumé

The aims of this study were to evaluate spectral detector CT (SDCT)-derived iodine concentration (IC) of lymph nodes diagnosed as metastatic and benign in prostate-specific membrane antigen (PSMA) PET/CT and to assess its potential use for lymph node assessment in prostate cancer. Thirty-four prostate cancer patients were retrospectively included: 16 patients with and 18 without lymph node metastases as determined by PSMA PET/CT. Patients underwent PSMA PET/CT as well as portal venous phase abdominal SDCT for clinical cancer follow-up. Only scan pairs with a stable nodal status indicated by constant size as well as comparable prostate-specific antigen (PSA) levels were included. One hundred benign and 96 suspected metastatic lymph nodes were annotated and correlated between SDCT and PSMA PET/CT. Iodine concentration in SDCT-derived iodine maps and SUVmax in ultra-high definition reconstructions from PSMA PET/CT were acquired based on the region of interest. Metastatic lymph nodes as per PSMA PET/CT showed higher IC than nonmetastatic nodes (1.9 ± 0.6 mg/mL vs 1.5 ± 0.5 mg/mL, P < 0.05) resulting in an AUC of 0.72 and sensitivity/specificity of 81.3%/58.5%. The mean short axis diameter of metastatic lymph nodes was larger than that of nonmetastatic nodes (6.9 ± 3.6 mm vs 5.3 ± 1.3 mm; P < 0.05); a size threshold of 1 cm short axis diameter resulted in a sensitivity/specificity of 12.8%/99.0%. There was a significant yet weak positive correlation between SUVmax and IC (rs = 0.25; P < 0.001). Spectral detector CT-derived IC was increased in lymph nodes diagnosed as metastatic in PSMA PET/CT yet showed considerable data overlap. The correlation between IC and SUVmax was weak, highlighting the role of PSMA PET/CT as important reference imaging modality for detection of lymph node metastases in prostate cancer patients.

Identifiants

pubmed: 33443954
doi: 10.1097/RLU.0000000000003496
pii: 00003072-202104000-00005
doi:

Substances chimiques

Antigens, Surface 0
Iodine Radioisotopes 0
FOLH1 protein, human EC 3.4.17.21
Glutamate Carboxypeptidase II EC 3.4.17.21

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

303-309

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest and sources of funding: Parts of this study have been supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) within the Priority Programme SPP 2177 Radiomics (PE 1711/2-1 to T.P.) and the Else Kröner-Fresenius-Stiftung (2016-Kolleg-19 to S.L. and EKMS_2018.34 to N.G.H.). A.D. received research support (material transfer) and speaker honorary from and is consulting for GE Healthcare; received research support from Life Molecular Imaging; received research support (material transfer), speaker honorary, and stock from and is consulting for Siemens Healthineers; and received research support (material transfer) from AVID/Lilly. The patent is pending for PET tracer PSMA-7. D.M. and N.G.H. received speaker honorary from Philips Healthcare. S.L., N.G.H., and D.Z. received research support from Philips Healthcare. No other potential conflicts of interest relevant to this article exist.

Références

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Auteurs

Philipp Täger (P)

Department of Nuclear Medicine, Faculty of Medicine, University Cologne.

David Zopfs (D)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

Andra-Iza Iuga (AI)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

Robert Peter Reimer (RP)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

Charlotte Zäske (C)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

Nils Große Hokamp (N)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

David Maintz (D)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

Axel Heidenreich (A)

Department of Urology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

Alexander Drzezga (A)

Department of Nuclear Medicine, Faculty of Medicine, University Cologne.

Carsten Kobe (C)

Department of Nuclear Medicine, Faculty of Medicine, University Cologne.

Thorsten Persigehl (T)

From the Institute for Diagnostic and Interventional Radiology, Faculty of Medicine, University Cologne and University Hospital Cologne, Cologne, Germany.

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