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Basic Science Investigation |
1 Inserm, U590, Lyon, France; 2 Département d'Anatomopathologie et Cytologie, Lyon, France; 3 Centre Léon Bérard, Lyon, France; 4 Service de Médecine Nucléaire, Centre Hospitalier Universitaire Dupuytren, Limoges, France; 5 Université de Lyon, Lyon, France; and 6 Institut d'Hématologie-Oncologie Pédiatrique, Lyon, France
Correspondence: For correspondence or reprints contact: Raphaël Rousseau, Institut d'Hématologie-Oncologie Pédiatrique, 1 Place Du Professeur Joseph Renaut, 69373 Lyon, Cedex 08, France. E-mail: dutoura{at}lyon.fnclcc.fr
Assessment of osteosarcoma response to neoadjuvant chemotherapy is performed by histopathologic analysis after surgical resection of the primary tumor. The purpose of this study was to evaluate whether 18F-FDG PET could be a noninvasive surrogate to histopathologic analysis and allow for earlier response evaluation to neoadjuvant chemotherapy in osteosarcoma. Methods: Metabolic response to neoadjuvant chemotherapy was assessed in immunocompetent rats with a preestablished orthotopic osteosarcoma using 18F-FDG PET before and after receiving 2 doses of ifosfamide. Comparison was then made by assessing histologic responses on euthanized animals. Results: Maximum standardized uptake value (SUVmax) measured by 18F-FDG PET after 2 doses of chemotherapy was correlated to histologic classification (P < 0.01). An SUVmax less than 15 corresponded to good responders, whereas an SUVmax greater than 15 but less than 20 and an SUVmax greater than 20 corresponded to partial responders or nonresponders, respectively. A 40% decrease in SUVmax between the first and second 18F-FDG PET scans distinguished between partial and good response to chemotherapy. Conclusion: Determination of SUVmax using semiquantitative 18F-FDG PET predicts response to neoadjuvant chemotherapy earlier than does histologic analysis.
Key Words: osteosarcoma histologic response 18F-FDG PET metabolic response SUVmax
* Contributed equally to this work.
COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.
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