Instrumentation factors affecting variance and bias of quantifying tracer uptake with PET/CT
Open accessAbstract
Purpose: The variances and biases inherent in quantifying PET tracer uptake from instrumentation factors are needed to ascertain the significance of any measured differences such as in quantifying response to therapy. The authors studied the repeatability and reproducibility of serial PET measures of activity as a function of object size, acquisition, reconstruction, and analysis method on one scanner and at three PET centers using a single protocol with long half‐life phantoms. Methods: The authors assessed standard deviations (SDs) and mean biases of consecutive measures of PET activity concentrations in a uniform phantom and a NEMA NU‐2 image quality (IQ) phantom filled with 9 months half‐life in an epoxy matrix. Activity measurements were normalized by dividing by a common decay corrected true value and reported as recovery coefficients (RCs). Each experimental set consisted of 20 consecutive PET scans of either a stationary phantom to evaluate repeatability or a repositioned phantom to assess reproducibility. One site conducted a comprehensive series of repeatability and reproducibility experiments, while two other sites repeated the reproducibility experiments using the same IQ phantom. An equation was derived to estimate the SD of a new PET measure from a known SD based on the ratios of available coincident counts between the two PET measures. Results: For stationary uniform phantom scans, the SDs of maximum RCs were three to five times less than predicted for uncorrelated pixels within circular regions of interest (ROIs) with diameters ranging from 1 to 15 cm. For stationary IQ phantom scans from 1 cm diameter ROIs, the average SDs of mean and maximum RCs ranged from 1.4% to 8.0%, depending on the methods of acquisition and reconstruction (coefficients of variation range 2.5% to 9.8%). Similar SDs were observed for both analytic and iterative reconstruction methods . SDs of RCs for 2D acquisitions were significantly higher than for 3D acquisitions for same acquisition and processing parameters. SDs of maximum RCs were larger than corresponding mean values for stationary IQ phantom scans , although the magnitude of difference is reduced due to noise correlations in the image. Increased smoothing decreased SDs and decreased maximum and mean RCs . Reproducibility of GE DSTE, Philips Gemini TF, and Siemens Biograph Hi‐REZ PET/CT scans of the same IQ phantom, with similar acquisition, reconstruction, and repositioning among 20 scans, were, in general, similar (mean and maximum RC SD range 2.5% to 4.8%). Conclusions: Short‐term scanner variability is low compared to other sources of error. There are tradeoffs in noise and bias depending on acquisition, processing, and analysis methods. The SD of a new PET measure can be estimated from a known SD if the ratios of available coincident counts between the two PET scanner acquisitions are known and both employ the same ROI definition. Results suggest it is feasible to use PET/CTs from different vendors and sites in clinical trials if they are properly cross‐calibrated.
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Using quantitative PET for patient selection is difficult in clinical practice because SUV measurements not obtained in a well-conducted clinical trial are subject to variability due to technical factors such as the PET scanner used and the acquisition and reconstruction parameters.
“Using quantitative PET for patient selection is difficult in clinical practice because SUV measurements not obtained in a well-conducted clinical trial are subject to variability. This is because of technical factors such as the PET scanner used and the acquisition and reconstruction parameters (23–26).”
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- Authors
- Doot, R. K., Scheuermann, J. S., Christian, P. E., Karp, J. S., & Kinahan, P. E.
- Affiliations
- University of Washington (US)
- University of Pennsylvania (US)
- University of Utah (US)
- Corresponding author
- Doot, R. K.
- Venue
- Medical Physics
- Publisher
- Wiley
- Published
- 2010-10-29
- Volume
- 37
- Issue
- 11
- Pages
- 6035-6046
- ISSN
- 0094-2405 (ISSN-L)
- 2473-4209
- PMC
- PMC2988835
- OpenAlex
- W1997504100
- Cited by
- 82
- References
- 41
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 2 · 2023: 1 · 2022: 6 · 2021: 6 · 2020: 4 · 2019: 6 · 2018: 9 · 2017: 6 · 2016: 8 · 2015: 4 · 2014: 6 · 2013: 5 · 2012: 8
- FWCI
- 4.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Medical Physics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- SNM Student Fellowship
- U.S. NCI (24XS036-004 (RIDER))
- U.S. NIH (CA74135, CA113941, CA115870, CA124573)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Cardiac Imaging and Diagnostics
- Physical Sciences › Physics and Astronomy › Radiation › Advanced Radiotherapy Techniques
- Keywords
- PET/CT, measurement variance, measurement bias, repeatability, reproducibility, recovery coefficient, object size, iterative reconstruction, image smoothing, noise correlation, coincidence counts, image quality phantom
- MeSH terms
- Air, Calibration, Equipment Design, Germanium, Humans, Image Processing, Computer-Assisted, Materials Testing, Radioisotopes, Tomography, X-Ray Computed, Water, Reproducibility of Results, Phantoms, Imaging, Imaging, Three-Dimensional, Positron-Emission Tomography
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