4.7 Article

Intra-individual comparison of 18F-sodium fluoride PET-CT and 99mTc bone scintigraphy with SPECT in patients with prostate cancer or breast cancer at high risk for skeletal metastases (MITNEC-A1): a multicentre, phase 3 trial

Journal

LANCET ONCOLOGY
Volume 23, Issue 12, Pages 1499-1507

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S1470-2045(22)00642-8

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Funding

  1. Canadian Institutes of Health Research through the Medical Imaging Trials Network of Canada (MITNEC) initiative

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This study compared the diagnostic performance of Tc-99m-MDP SPECT and F-18-NaF PET-CT for detecting bone metastases in high-risk prostate or breast cancer patients. The results showed that F-18-NaF PET-CT had a higher accuracy. This study is clinically significant.
Background Detection of skeletal metastases in patients with prostate cancer or breast cancer remains a major clinical challenge. We aimed to compare the diagnostic performance of Tc-99m-methylene diphosphonate (Tc-99m-MDP) single-photon emission CT (SPECT) and F-18-sodium fluoride (F-18-NaF) PET-CT for the detection of osseous metastases in patients with high-risk prostate or breast cancer. Methods MITNEC-A1 was a prospective, multicentre, single-cohort, phase 3 trial conducted in ten hospitals across Canada. Patients aged 18 years or older with breast or prostate cancer with a WHO performance status of 0-2 and with high risk or clinical suspicion for bone metastasis, but without previously documented bone involvement, were eligible. F-18-NaF PET-CT and Tc-99m-MDP SPECT were done within 14 days of each other for each participant. Two independent reviewers interpreted each modality without knowledge of other imaging findings. The primary endpoint was the overall accuracy of Tc-99m-MDP SPECT and F-18-NaF PET-CT scans for the detection of bone metastases in the per-protocol population. A combination of histopathological, clinical, and imaging follow-up for up to 24 months was used as the reference standard to assess the imaging results. Safety was assessed in all enrolled participants. This study is registered with ClinicalTrials.gov, NCT01930812, and is complete. Findings Between July 11, 2014, and March 3, 2017, 290 patients were screened, 288 of whom were enrolled (64 participants with breast cancer and 224 with prostate cancer). 261 participants underwent both F-18-NaF PET-CT and Tc-99m-MDP SPECT and completed the required follow-up for statistical analysis. Median follow-up was 735 days (IQR 727-750). Based on the reference methods used, 109 (42%) of 261 patients had bone metastases. In the patient-based analysis, F-18-NaF PET-CT was more accurate than Tc-99m-MDP SPECT (84 center dot 3% [95% CI 79 center dot 9-88 center dot 7] vs 77 center dot 4% [72 center dot 3-82 center dot 5], difference 6 center dot 9% [95% CI 1 center dot 3-12 center dot 5]; p=0 center dot 016). No adverse events were reported for the 288 patients recruited. Interpretation F-18-NaF has the potential to displace Tc-99m-MDP as the bone imaging radiopharmaceutical of choice in patients with high-risk prostate or breast cancer. Copyright (c) 2022 Published by Elsevier Ltd. All rights reserved.

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