18F-FDG PET/CT as an Indicator of Progression-Free and Overall Survival in Osteosarcoma

被引:140
作者
Costelloe, Colleen M. [1 ]
Macapinlac, Horner A. [2 ]
Madewell, John E. [1 ]
Fitzgerald, Nancy E. [1 ]
Mawlawi, Osama R. [3 ]
Rohren, Eric M. [2 ]
Raymond, A. Kevin [4 ]
Lewis, Valerae O. [5 ]
Anderson, Peter M. [6 ]
Bassett, Roland L., Jr. [7 ]
Harrell, Robyn K. [7 ]
Marom, Edith M. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Unit 1273, Dept Radiol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Nucl Med, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Orthoped Oncol, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Pediat, Houston, TX 77030 USA
[7] Univ Texas MD Anderson Canc Ctr, Div Biostat, Houston, TX 77030 USA
关键词
molecular imaging; PET; PET/CT; F-18-FDG; osteosarcoma; survival; tumor necrosis; DEDIFFERENTIATED PAROSTEAL OSTEOSARCOMA; TARGET VOLUME DEFINITION; GROSS TUMOR VOLUME; EMISSION-TOMOGRAPHY; COOPERATIVE OSTEOSARCOMA; PROGNOSTIC-SIGNIFICANCE; CHEMOTHERAPY RESPONSE; THERAPEUTIC RESPONSE; OSTEOGENIC-SARCOMA; FOLLOW-UP;
D O I
10.2967/jnumed.108.058461
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The aim of our study was to retrospectively evaluate whether maximum standardized uptake value (SUVmax), total lesion gylcolysis (TLG), or change therein using F-18-FDG PET/CT performed before and after initial chemotherapy were indicators of patient outcome. Methods: Thirty-one consecutive patients who underwent F-18-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 A 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: F-18-FDG PET/CT can be used as a prognostic indicator for progression-free survival, overall survival, and tumor necrosis in osteosarcoma.
引用
收藏
页码:340 / 347
页数:8
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