Journal article
Effect of F-18-Fluciclovine Positron Emission Tomography on the Management of Patients With Recurrence of Prostate Cancer: Results From the FALCON Trial
International journal of radiation oncology, biology, physics, Vol.107(2), pp.316-324
06/01/2020
DOI: 10.1016/j.ijrobp.2020.01.050
PMID: 32068113
Abstract
Purpose: Early and accurate localization of lesions in patients with biochemical recurrence (BCR) of prostate cancer may guide salvage therapy decisions. The present study, F-18-Fluciclovine PET/CT in biochemicAL reCurrence Of Prostate caNcer (FALCON; NCT02578940), aimed to evaluate the effect of F-18-fluciclovine on management of men with BCR of prostate cancer.
Methods and Materials: Men with a first episode of BCR after curative-intent primary therapy were enrolled at 6 UK sites. Patients underwent F-18-fluciclovine positron emission tomography/computed tomography (PET/CT) according to standardized procedures. Clinicians documented management plans before and after scanning, recording changes to treatment modality as major and changes within a modality as other. The primary outcome measure was record of a revised management plan postscan. Secondary endpoints were evaluation of optimal prostate specific antigen (PSA) threshold for detection, salvage treatment outcome assessment based on F-18-fluciclovine-involvement, and safety.
Results: F-18-Fluciclovine was well tolerated in the 104 scanned patients (median PSA = 0.79 ng/mL). Lesions were detected in 58 out of 104 (56%) patients. Detection was broadly proportional to PSA level; <= 1 ng/mL, 1 out of 3 of scans were positive, and 93% scans were positive at PSA >2.0 ng/mL. Sixty-six (64%) patients had a postscan management change (80% after a positive result). Major changes (43 out of 66; 65%) were salvage or systemic therapy to watchful waiting (16 out of 66; 24%); salvage therapy to systemic therapy (16 out of 66; 24%); and alternative changes to treatment modality (11 out of 66, 17%). The remaining 23 out of 66 (35%) management changes were modifications of the prescan plan: most (22 out of 66; 33%) were adjustments to planned brachytherapy/radiation therapy to include a F-18-fluciclovine-guided boost. Where F-18-fluciclovine guided salvage therapy, the PSA response rate was higher than when F-18-fluciclovine was not involved (15 out of 17 [88%] vs 28 out of 39 [72%]).
Conclusions: F-18-Fluciclovine PET/CT located recurrence in the majority of men with BCR, frequently resulting in major management plan changes. Incorporating F-18-fluciclovine PET/CT into treatment planning may optimize targeting of recurrence sites and avoid futile salvage therapy. (C) 2020 The Authors. Published by Elsevier Inc.
Details
- Title: Subtitle
- Effect of F-18-Fluciclovine Positron Emission Tomography on the Management of Patients With Recurrence of Prostate Cancer: Results From the FALCON Trial
- Creators
- Andrew F. Scarsbrook - Leeds Teaching Hospitals NHS TrustDavid Bottomley - Leeds Teaching Hospitals NHS TrustEugene J. Teoh - Blue Earth DiagnosticsKevin M. Bradley - PETIC, Wales Research and Diagnostic PET Imaging Centre, Cardiff, United KingdomHeather Payne - University College London Hospitals NHS Foundation TrustAsim Afaq - University College London Hospitals NHS Foundation TrustJamshed Bomanji - University College London Hospitals NHS Foundation TrustNicholas van As - Royal Marsden NHS Foundation TrustSue Chua - Royal Marsden NHS Foundation TrustPeter Hoskin - Mount Vernon Cancer CentreAnthony Chambers - Mount Vernon Cancer CentreGary J. Cook - St Thomas' HospitalVictoria S. Warbey - St Thomas' HospitalSai Han - Gartnavel General HospitalHing Y. Leung - University of GlasgowAlbert Chau - Blue Earth DiagnosticsMatthew P. Miller - Blue Earth DiagnosticsFergus Gleeson - Departments of Radiology and Nuclear Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, United KingdomGerard Andrade - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandPhilip Camilieri - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandKatherine Hyde - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandRuth Macpherson - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandNeel Patel - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandAmi Sabharwal - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandManil Subesinghe - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandMaria Tsakok - Oxford Univ Hosp NHS Fdn Trust, Dept Radiol, Oxford, EnglandFALCON Study Group
- Resource Type
- Journal article
- Publication Details
- International journal of radiation oncology, biology, physics, Vol.107(2), pp.316-324
- DOI
- 10.1016/j.ijrobp.2020.01.050
- PMID
- 32068113
- NLM abbreviation
- Int J Radiat Oncol Biol Phys
- ISSN
- 0360-3016
- eISSN
- 1879-355X
- Publisher
- Elsevier Inc
- Number of pages
- 9
- Grant note
- Innovate UK; UK Research & Innovation (UKRI) Blue Earth Diagnostics, Oxford, UK
- Language
- English
- Date published
- 06/01/2020
- Academic Unit
- Radiology
- Record Identifier
- 9984318792502771
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