Impact of time-of-flight and point-spread-function in SUV quantification for oncological PET

Clin Nucl Med. 2013 Feb;38(2):103-9. doi: 10.1097/RLU.0b013e318279b9df.

Abstract

Background: Accuracy in the quantification of the SUV is a critical point in PET because proper quantification of tumor uptake is essential for therapy monitoring and prognosis evaluation. Recent advances such as time-of-flight (TOF) and point-spread-function (PSF) reconstructions have dramatically improved detectability. However, first experiences with these techniques have shown a consistent tendency to measure markedly high SUV values, bewildering nuclear medicine physicians and referring clinicians.

Purpose: We investigated different reconstruction and quantification procedures to determine the optimum protocol for an accurate SUV quantification in last generation PET scanners.

Methods: Both phantom and patient images were evaluated. A complete set of experiments was performed using a body phantom containing 6 spheres with different background levels and contrasts. Whole-body FDG PET/CT of 20 patients with breast and lung cancer was evaluated. One hundred five foci were identified by 2 experienced nuclear medicine physicians.Each acquisition was reconstructed both with classical and advanced (TOF, PSF) reconstruction techniques. Each sphere and each in vivo lesion was quantified with different parameters as follows: SUV(max), SUV(mean), and SUV(50) (mean within a 50% isocontour).

Results: This study has confirmed that quantification with SUV(max) produces important overestimation of metabolism in new generation PET scanners. This is a relevant result because, currently, SUV(max) is the standard parameter for quantification. SUV(50) has been shown as the best alternative, especially when applied to images reconstructed with PSF + TOF.

Conclusions: SUV(50) provides accurate quantification and should replace SUV(max) in PET tomographs incorporating advanced reconstruction techniques. PSF + TOF reconstruction is the optimum for both detection and accurate quantification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Breast Neoplasms / diagnostic imaging*
  • Breast Neoplasms / metabolism
  • Humans
  • Image Processing, Computer-Assisted / methods*
  • Lung Neoplasms / diagnostic imaging*
  • Lung Neoplasms / metabolism
  • Multimodal Imaging / methods*
  • Phantoms, Imaging
  • Positron-Emission Tomography*
  • Time Factors
  • Tomography, X-Ray Computed*
  • Whole Body Imaging