A PET/MRI study towards finding the optimal [18F]Fluciclovine PET protocol for detection and characterisation of primary prostate cancer

  • Mattijs Elschot
  • Kirsten M. Selnæs
  • Elise Sandsmark
  • Brage Krüger-Stokke
  • Øystein Størkersen
  • May-Britt Tessem
  • Siver A. Moestue
  • Helena Bertilsson
  • Tone F. Bathen
Original Article

Abstract

Purpose

[18F]Fluciclovine PET imaging shows promise for the assessment of prostate cancer. The purpose of this PET/MRI study is to optimise the PET imaging protocol for detection and characterisation of primary prostate cancer, by quantitative evaluation of the dynamic uptake of [18F]Fluciclovine in cancerous and benign tissue.

Methods

Patients diagnosed with high-risk primary prostate cancer underwent an integrated [18F]Fluciclovine PET/MRI exam before robot-assisted radical prostatectomy with extended pelvic lymph node dissection. Volumes-of-interest (VOIs) of selected organs (prostate, bladder, blood pool) and sub-glandular prostate structures (tumour, benign prostatic hyperplasia (BPH), inflammation, healthy tissue) were delineated on T2-weighted MR images, using whole-mount histology samples as a reference. Three candidate windows for optimal PET imaging were identified based on the dynamic curves of the mean and maximum standardised uptake value (SUVmean and SUVmax, respectively). The statistical significance of differences in SUV between VOIs were analysed using Wilcoxon rank sum tests (p<0.05, adjusted for multiple testing).

Results

Twenty-eight (28) patients [median (range) age: 66 (55-72) years] were included. An early (W1: 5-10 minutes post-injection) and two late candidate windows (W2: 18-23; W3: 33-38 minutes post-injection) were selected. Late compared with early imaging was better able to distinguish between malignant and benign tissue [W3, SUVmean: tumour vs. BPH 2.5 vs. 2.0 (p<0.001), tumour vs. inflammation 2.5 vs. 1.7 (p<0.001), tumour vs. healthy tissue 2.5 vs. 2.0 (p<0.001); W1, SUVmean: tumour vs. BPH 3.1 vs. 3.1 (p=0.771), tumour vs inflammation 3.1 vs. 2.2 (p=0.021), tumour vs. healthy tissue 3.1 vs. 2.5 (p<0.001)] as well as between high-grade and low/intermediate-grade tumours (W3, SUVmean: 2.6 vs. 2.1 (p=0.040); W1, SUVmean: 3.1 vs. 2.8 (p=0.173)). These differences were relevant to the peripheral zone, but not the central gland.

Conclusion

Late-window [18F]Fluciclovine PET imaging shows promise for distinguishing between prostate tumours and benign tissue and for assessment of tumour aggressiveness.

Keywords

[18F]Fluciclovine [18F]FACBC Prostate Cancer PET/MRI Dynamic PET 

Supplementary material

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ESM 1(DOCX 12 kb)
259_2016_3562_MOESM2_ESM.docx (213 kb)
ESM 2(DOCX 212 kb)

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Copyright information

© Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  • Mattijs Elschot
    • 1
  • Kirsten M. Selnæs
    • 1
    • 2
  • Elise Sandsmark
    • 1
  • Brage Krüger-Stokke
    • 1
    • 3
  • Øystein Størkersen
    • 4
  • May-Britt Tessem
    • 1
  • Siver A. Moestue
    • 1
    • 5
  • Helena Bertilsson
    • 6
    • 7
  • Tone F. Bathen
    • 1
    • 2
  1. 1.Deparment of Circulation and Medical Imaging, Faculty of MedicineNTNU, Norwegian University of Science and TechnologyTrondheimNorway
  2. 2.St. Olavs HospitalTrondheim University HospitalTrondheimNorway
  3. 3.Department of Radiology, St. Olavs HospitalTrondheim University HospitalTrondheimNorway
  4. 4.Department of Pathology, St. Olavs HospitalTrondheim University HospitalTrondheimNorway
  5. 5.Department of Laboratory Medicine, Children’s and Women’s Health, Faculty of MedicineNTNU, Norwegian University of Science and TechnologyTrondheimNorway
  6. 6.Department of Urology, St. Olavs HospitalTrondheim University HospitalTrondheimNorway
  7. 7.Department of Cancer Research and Molecular Medicine, Faculty of MedicineNTNU, Norwegian University of Science and TechnologyTrondheimNorway

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