Published November 1, 2012 | Version v1
Journal article

Positron Emission Tomography/Computed Tomography Imaging of Residual Skull Base Chordoma Before Radiotherapy Using Fluoromisonidazole and Fluorodeoxyglucose: Potential Consequences for Dose Painting

  • 1. CNRS-UMR 6543, Institute of Developmental Biology and Cancer, University of Nice Sophia Antipolis, Nice (France)
  • 2. Radiation Oncology Department, Antoine Lacassagne Center, Nice (France)
  • 3. Department of Nuclear Medicine and Radiopharmacy, Tenon Hospital, and University Pierre et Marie Curie, Paris (France)
  • 4. Proton Therapy Center of Orsay, Curie Institute, Paris (France)
  • 5. Department of Neurosurgery, Pitié-Salpêtrière Hospital, Paris (France)
  • 6. Department of Neurosurgery, Adolph De Rothschild Foundation, Paris (France)
  • 7. Department of Neurosurgery, Lariboisière Hospital, Paris (France)
  • 8. Department of Pathology, Lariboisière Hospital, Paris (France)
  • 9. Department of Pathology, Pitié-Salpêtrière Hospital, Paris (France)

Description

Purpose: To detect the presence of hypoxic tissue, which is known to increase the radioresistant phenotype, by its uptake of fluoromisonidazole (18F) (FMISO) using hybrid positron emission tomography/computed tomography (PET/CT) imaging, and to compare it with the glucose-avid tumor tissue imaged with fluorodeoxyglucose (18F) (FDG), in residual postsurgical skull base chordoma scheduled for radiotherapy. Patients and Methods: Seven patients with incompletely resected skull base chordomas were planned for high-dose radiotherapy (dose ≥70 Gy). All 7 patients underwent FDG and FMISO PET/CT. Images were analyzed qualitatively by visual examination and semiquantitatively by computing the ratio of the maximal standardized uptake value (SUVmax) of the tumor and cerebellum (T/C R), with delineation of lesions on conventional imaging. Results: Of the eight lesion sites imaged with FDG PET/CT, only one was visible, whereas seven of nine lesions were visible on FMISO PET/CT. The median SUVmax in the tumor area was 2.8 g/mL (minimum 2.1; maximum 3.5) for FDG and 0.83 g/mL (minimum 0.3; maximum 1.2) for FMISO. The T/C R values ranged between 0.30 and 0.63 for FDG (median, 0.41) and between 0.75 and 2.20 for FMISO (median,1.59). FMISO T/C R >1 in six lesions suggested the presence of hypoxic tissue. There was no correlation between FMISO and FDG uptake in individual chordomas (r = 0.18, p = 0.7). Conclusion: FMISO PET/CT enables imaging of the hypoxic component in residual chordomas. In the future, it could help to better define boosted volumes for irradiation and to overcome the radioresistance of these lesions. No relationship was founded between hypoxia and glucose metabolism in these tumors after initial surgery.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2011.12.047

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2011.12.047;
PII
S0360-3016(11)03735-7;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
84
Journal Issue
3
Journal Page Range
p. 681-687
ISSN
0360-3016
CODEN
IOBPD3

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.