Practical approach for comparative analysis of multilesion molecular imaging using a semiautomated program for PET/CT. Academic Article uri icon

Overview

abstract

  • UNLABELLED: We propose a standardized approach to quantitative molecular imaging (MI) in cancer patients with multiple lesions. METHODS: Twenty patients with castration-resistant prostate cancer underwent (18)F-FDG and (18)F-16β-fluoro-5-dihydrotestosterone ((18)F-FDHT) PET/CT scans. Using a 5-point confidence scale, 2 readers interpreted coregistered scan sets on a workstation. Two hundred three sites per scan (specified in a lexicon) were reviewed. (18)F-FDG-positive lesion bookmarks were propagated onto (18)F-FDHT studies and then manually accepted or rejected. Discordance-positive (18)F-FDHT lesions were similarly bookmarked. Lesional SUV(max) was recorded. Tracer- and tissue-specific background correction factors were calculated via receiver-operating-characteristic analysis of 65 scan sets. RESULTS: Readers agreed on more than 99% of (18)F-FDG- and (18)F-FDHT-negative sites. Positive-site agreement was 83% and 85%, respectively. Consensus-lesion maximum standardized uptake value (SUV(max)) was highly reproducible (concordance correlation coefficient > 0.98). Receiver-operating-characteristic curves yielded 4 correction factors (SUV(max) 1.8-2.6). A novel scatterplot (Larson-Fox-Gonen plot) depicted tumor burden and change in SUV(max) for response assessments. CONCLUSION: Multilesion molecular imaging is optimized with a 5-step approach incorporating a confidence scale, site lexicon, semiautomated PET software, background correction, and Larson-Fox-Gonen graphing.

publication date

  • October 7, 2011

Research

keywords

  • Image Processing, Computer-Assisted
  • Molecular Imaging
  • Multimodal Imaging
  • Positron-Emission Tomography
  • Prostatic Neoplasms
  • Tomography, X-Ray Computed

Identity

PubMed Central ID

  • PMC3409842

Scopus Document Identifier

  • 80455168438

Digital Object Identifier (DOI)

  • 10.2967/jnumed.111.089326

PubMed ID

  • 21984797

Additional Document Info

volume

  • 52

issue

  • 11