Bone Metastases Clinical Trial
Official title:
18F-Fluoride PET/CT Versus 99mTc-MDP Scanning for Detecting Bone Metastases: A Randomized, Multi-Center Trial to Compare Two Bone Imaging Techniques
The primary objective is to compare the diagnostic performance of 18F- Fluoride PET/CT scanning to that of conventional bone scanning for detecting cancer that has spread to the bone (bone metastasis). The intent of the study is to determine whether 18F-Fluoride PET/CT will lead to improved treatment and patient outcomes.
The trial will accrue four hundred-eighty eight (488) evaluable patients with breast cancer,
prostate cancer or lung cancer (approximately 163 of each cancer type) referred for routine
bone scanning by their respective physicians. The specific stages of cancer required for
eligibility are described in the eligibility criteria.
Approximately eleven to fifteen qualified clinical centers will participate in the trial,
with target enrollment for each site set at roughly 40-50 patients per site.
The images of the patients will be transmitted to ACR Image Metrix, an imaging contract
research organization (iCRO), for quality assurance and archival. iCRO will conduct blinded
core lab interpretations by 3 radiologists who have not been involved in the design of the
trial nor the clinical image interpretation. The data from the core lab readings will be
compared with the deliberations of a multidisciplinary panel of oncology experts who will be
blinded to the initial scan results and will determine the standard of evidence (truth) for
each patient. The analysis will be based on this comparison.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Diagnostic
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