18F-FDG PET/CT as an Indicator of Progression-Free and Overall Survival in Osteosarcoma
Authors:
- Colleen M. CostelloeCCColleen M. Costelloe
- Homer A. MacapinlacHMHomer A. Macapinlac
- John E. MadewellJMJohn E. Madewell
- Nancy E. FitzgeraldNFNancy E. Fitzgerald
- Osama R. MawlawiOMOsama R. Mawlawi
- Eric M. RohrenEREric M. Rohren
- A. Kevin RaymondARA. Kevin Raymond
- Valerae O. LewisVLValerae O. Lewis
- Peter M. AndersonPAPeter M. Anderson
- Roland L. BassettRBRoland L. Bassett
- Robyn K. HarrellRHRobyn K. Harrell
- Edith M. MaromEMEdith M. Marom
Open Access
- 2 March 2009
- journal article
- Published by Society of Nuclear Medicine in Journal of Nuclear Medicine
- Vol. 50 (3) , 340-347
Abstract
The aim of our study was to retrospectively evaluate whether maximum standardized uptake value (SUVmax), total lesion gylcolysis (TLG), or change therein using 18F-FDG PET/CT performed before and after initial chemotherapy were indicators of patient outcome. Methods: Thirty-one consecutive patients who underwent 18F-FDG PET/CT before and after chemotherapy, followed by tumor resection, were retrospectively reviewed. Univariate Cox regression was used to analyze for relationships between covariates of interest (SUVmax before and after chemotherapy, change in SUVmax, TLG before and after chemotherapy, change in TLG, and tumor necrosis) and progression-free and overall survival. Logistic regression was used to evaluate tumor necrosis. Results: High SUVmax before and after chemotherapy (P = 0.008 and P = 0.009, respectively) was associated with worse progression-free survival. The cut point for SUVmax before chemotherapy was greater than 15 g/mL* (P = 0.015), and after chemotherapy it was greater than 5 g/mL* (P = 0.006), as measured at our institution and using lean body mass. Increase in TLG after chemotherapy was associated with worse progression-free survival (P = 0.016). High SUVmax after chemotherapy was associated with poor overall survival (P = 0.035). The cut point was above the median of 3.3 g/mL* (P = 0.043). High TLG before chemotherapy was associated with poor overall survival (P = 0.021). Good overall and progression-free survival was associated with a tumor necrosis greater than 90% (P = 0.018 and 0.08, respectively). A tumor necrosis greater than 90% was most strongly associated with a decrease in SUVmax (P = 0.015). Conclusion: 18F-FDG PET/CT can be used as a prognostic indicator for progression-free survival, overall survival, and tumor necrosis in osteosarcoma.Keywords
This publication has 33 references indexed in Scilit:
- Prognostic significance of 18F-FDG uptake in primary osteosarcoma after but not before chemotherapy: a possible association with autocrine motility factor/phosphoglucose isomerase expressionClinical & Experimental Metastasis, 2008
- Telangiectatic osteosarcoma: The St. Jude Children's Research Hospital's experienceCancer, 2007
- Large Institutional Experience with Dose-Intensive Chemotherapy and Stem Cell Support in the Management of Sarcoma PatientsOncology, 2007
- Outcome of Postradiation Osteosarcoma Does Not Correlate with Chemotherapy ResponseClinical Orthopaedics and Related Research, 2006
- Pre- and post-chemotherapy alkaline phosphatase levels as prognostic indicators in adults with localised osteosarcomaEuropean Journal of Cancer, 2005
- Prognostic and therapeutic relevance of HER2 expression in osteosarcoma and Ewing’s sarcomaEuropean Journal of Cancer, 2005
- Dedifferentiated parosteal osteosarcoma: The experience of the Rizzoli InstituteCancer, 2005
- Evaluation of chemotherapy response in pediatric bone sarcomas by [F‐18]‐fluorodeoxy‐D‐glucose positron emission tomographyCancer, 2002
- Survival, prognosis, and therapeutic response in osteogenic sarcoma. The memorial hospital experienceCancer, 1992
- Effect of cumulative courses of intraarterial cis-diamminedichloroplatin-ii on the primary tumor in osteosarcomaCancer, 1989