Literature DB >> 29447047

Prospective comparative study of 18F-sodium fluoride PET/CT and planar bone scintigraphy for treatment response assessment of bone metastases in patients with prostate cancer.

Randi Fuglsang Fonager1,2, Helle Damgaard Zacho1,2, Niels Christian Langkilde3, Joan Fledelius4, June Anita Ejlersen4, Helle Westergreen Hendel5, Christian Haarmark5, Mette Moe6, Jesper Carl Mortensen4, Mads Ryø Jochumsen7, Lars Jelstrup Petersen1,2.   

Abstract

AIM: To compare 18F-sodium fluoride positron emission tomography/computed tomography (NaF PET/CT) and 99mTc-labelled diphosphonate bone scan (BS) for the monitoring of bone metastases in patients with prostate cancer undergoing anti-cancer treatment.
MATERIAL AND METHODS: Data from 64 patients with prostate cancer were included. The patients received androgen-deprivation therapy (ADT), next-generation hormonal therapy (NGH) or chemotherapy. The patients had a baseline scan and 1-3 subsequent scans during six months of treatment. Images were evaluated by experienced nuclear medicine physicians and classified for progressive disease (PD) or non-PD according to the Prostate Cancer Working Group 2 (PCWG-2) criteria. The patients were also classified as having PD/non-PD according to the clinical and prostate-specific antigen (PSA) responses.
RESULTS: There was no difference between NaF PET/CT and BS in the detection of PD and non-PD during treatment (McNemar's test, p = .18). The agreement between BS and NaF PET/CT for PD/non-PD was moderate (Cohen's kappa 0.53, 95% confidence interval 0.26-0.79). Crude agreement between BS and NaF PET/CT for the assessment of PD/non-PD was 86% (89% for ADT, n = 28; 88% for NGH, n = 16, and 80% for chemotherapy, n = 20). In most discordant cases, BS found PD when NaF PET/CT did not, or BS detected PD on an earlier scan than NaF PET/CT. Biochemical progression (27%) occurred more frequently than progression on functional imaging (BS, 22% and NaF PET/CT, 14%). Clinical progression was rare (11%), and almost exclusively seen in patients receiving chemotherapy.
CONCLUSION: There was no difference between NaF PET/CT and BS in the detection of PD and non-PD; however, BS seemingly detects PD by the PCWG-2 criteria earlier than NaF-PET, which might be explained by the fact that NaF-PET is more sensitive at the baseline scan.

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Year:  2018        PMID: 29447047     DOI: 10.1080/0284186X.2018.1438651

Source DB:  PubMed          Journal:  Acta Oncol        ISSN: 0284-186X            Impact factor:   4.089


  5 in total

1.  Prospective comparison of 68Ga-PSMA PET/CT, 18F-sodium fluoride PET/CT and diffusion weighted-MRI at for the detection of bone metastases in biochemically recurrent prostate cancer.

Authors:  Helle D Zacho; Julie B Nielsen; Ali Afshar-Oromieh; Uwe Haberkorn; Nandita deSouza; Katja De Paepe; Katja Dettmann; Niels C Langkilde; Christian Haarmark; Rune V Fisker; Dennis T Arp; Jesper Carl; Jørgen B Jensen; Lars J Petersen
Journal:  Eur J Nucl Med Mol Imaging       Date:  2018-06-06       Impact factor: 9.236

2.  Radiomics for detecting prostate cancer bone metastases invisible in CT: a proof-of-concept study.

Authors:  Ricarda Hinzpeter; Livia Baumann; Roman Guggenberger; Martin Huellner; Hatem Alkadhi; Bettina Baessler
Journal:  Eur Radiol       Date:  2021-09-24       Impact factor: 7.034

3.  Observer Agreement and Accuracy of 18F-Sodium Fluoride PET/CT in the Diagnosis of Bone Metastases in Prostate Cancer.

Authors:  Helle D Zacho; Randi F Fonager; Julie B Nielsen; Christian Haarmark; Helle W Hendel; Martin B Johansen; Jesper C Mortensen; Lars J Petersen
Journal:  J Nucl Med       Date:  2019-09-03       Impact factor: 11.082

4.  Uptake in non-affected bone tissue does not differ between [18F]-DCFPyL and [68Ga]-HBED-CC PSMA PET/CT.

Authors:  Jochen Hammes; Melanie Hohberg; Philipp Täger; Markus Wild; Boris Zlatopolskiy; Philipp Krapf; Bernd Neumaier; Klaus Schomäcker; Carsten Kobe; Matthias Schmidt; Markus Dietlein; Alexander Drzezga
Journal:  PLoS One       Date:  2018-12-20       Impact factor: 3.240

Review 5.  Salvage therapy for prostate cancer after radical prostatectomy.

Authors:  Nicholas G Zaorsky; Jeremie Calais; Stefano Fanti; Derya Tilki; Tanya Dorff; Daniel E Spratt; Amar U Kishan
Journal:  Nat Rev Urol       Date:  2021-08-06       Impact factor: 14.432

  5 in total

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