Recurrent prostate cancer after radical prostatectomy: restaging performance of 18F-choline hybrid PET/MRI.


Journal

Medical oncology (Northwood, London, England)
ISSN: 1559-131X
Titre abrégé: Med Oncol
Pays: United States
ID NLM: 9435512

Informations de publication

Date de publication:
12 Jun 2019
Historique:
received: 15 04 2019
accepted: 07 06 2019
entrez: 14 6 2019
pubmed: 14 6 2019
medline: 9 10 2019
Statut: epublish

Résumé

To evaluate the diagnostic performance of a whole-body 18F-choline (FCH) hybrid PET/MRI for prostate cancer patients at biochemical relapse after radical prostatectomy (RP) compared to pelvic multiparametric MRI (mpMRI), one of the standard imaging modality for this patient population. From 2010 to 2016, 58 whole-body FCH PET/MRI studies with mpMRI acquisitions were performed in 53 prostate cancer patients relapsing after curative RP. Median PSA and PSA doubling time (PSA DT) at PET study were 1.5 ng/ml and 6.5 months, respectively. The overall positivity rate of FCH PET/MRI was 58.6% (n = 34), dropping to 44% in patients with a PSA ≤ 2 ng/ml (n = 36). Median PSA values in positive and negative PET/MRI studies were 2.2 ng/ml and 0.8 ng/ml, respectively, with no differences in PSA DT (6.5 vs. 6.6 months). A PSA value ≥ 1.5 ng/ml was a significant predictor of positivity on PET/MRI studies. Compared to PET, mpMRI identified more local relapses (17 vs. 14, p = 0.453) while PET outperformed whole-body Dixon MRI for regional (16 vs. 9, p = 0.016) and distant (12 vs. 6, p = 0.031) metastases. Compared to pelvic mpMRI, the treatment approach turned out to be influenced more frequently using whole-body FCH hybrid PET/MRI studies (58.6% vs. 38%). In prostate cancer patients with biochemical recurrence after RP, whole-body FCH PET/MRI achieved a higher detection rate of nodal/distant metastases compared to pelvic mpMRI alone, increasing the change of treatment strategy by more than 20%.

Identifiants

pubmed: 31190232
doi: 10.1007/s12032-019-1291-z
pii: 10.1007/s12032-019-1291-z
doi:

Substances chimiques

Fluorine Radioisotopes 0
Radiopharmaceuticals 0
fluoromethylcholine 0
Choline N91BDP6H0X

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

67

Subventions

Organisme : Fondation pour la lutte contre le cancer et pour des recherches médico-biologiques, Geneva, Switzerland.
ID : Fondation pour la lutte contre le cancer et pour des recherches médico-biologiques, Geneva, Switzerland.

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Auteurs

Verane Achard (V)

Radiation Oncology Division, Geneva University Hospital, 1211, Geneva 14, Switzerland.

Giorgio Lamanna (G)

Radiation Oncology Division, Geneva University Hospital, 1211, Geneva 14, Switzerland.

Antoine Denis (A)

Nuclear Medicine, Geneva University Hospital, Geneva, Switzerland.

Thomas De Perrot (T)

Radiology, Geneva University Hospital, Geneva, Switzerland.

Ismini Charis Mainta (IC)

Nuclear Medicine, Geneva University Hospital, Geneva, Switzerland.

Osman Ratib (O)

Nuclear Medicine, Geneva University Hospital, Geneva, Switzerland.

Christophe Iselin (C)

Urology, Geneva University Hospital, Geneva, Switzerland.

Raymond Miralbell (R)

Radiation Oncology Division, Geneva University Hospital, 1211, Geneva 14, Switzerland.

Valentina Garibotto (V)

Nuclear Medicine, Geneva University Hospital, Geneva, Switzerland.

Thomas Zilli (T)

Radiation Oncology Division, Geneva University Hospital, 1211, Geneva 14, Switzerland. Thomas.Zilli@hcuge.ch.

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Classifications MeSH