The objective of this study is to evaluate the utility of positron emission tomography (PET) with 2-deoxy-[(18)F] fl uoro-D-glucose (FDG) in the assessment of the chemotherapy response of osteosarcoma when compared with the degree of necrosis determined histologically. Whole-body FDG-PET scan was performed on 11 patients with osteosarcoma. All patients received neoadjuvant chemotherapy. The tumor size changes on magnetic resonance imaging; FDG-PET standardized uptake values prior to (SUV(1)) and following (SUV(2)) chemotherapy were analyzed and correlated with response to chemotherapy as assessed using histopathology in surgically excised tumors. Nine patients underwent FDG-PET scan both prior to and following neoadjuvant chemotherapy. The remaining two patients were examined only prior to surgery. Histologically, five patients had a good histologic response to chemotherapy (a parts per thousand 90% necrosis). The changes in tumor size did not correlate with histologic response (P > 0.05). SUV(2) with good response was significantly lower than that with poor response (1.93 +/- 0.50, 5.86 +/- 2.55, respectively). Both the positive and negative predictive values of the SUV(2) of less than 2.5 for a good response were 100%. Patients with good response showed a significantly higher ratio of SUV2 to SUV1 (SUV(2:1)) than patients with poor response (0.74 +/- 0.11, 0.26 +/- 0.39, respectively, P < 0.05). The positive and negative predictive values of SUV(2:1) a parts per thousand currency sign 0.5 for good and poor responses were 80% and 100%, respectively. FDG-PET imaging of osteosarcoma correlates positively with histologic response to neoadjuvant chemotherapy. SUV(2) and SUV(2:1) could be feasible as non-invasive surrogate predictors of response in osteosarcoma patients.
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Korea Canc Ctr Hosp, Dept Nucl Med, Seoul 139706, South Korea
Korea Inst Radiol & Med Sci, Dept Mol Imaging Ctr, Seoul, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Cheon, Gi Jeong
Kim, Min Suk
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Korea Canc Ctr Hosp, Dept Pathol, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Kim, Min Suk
Lee, Jun Ah
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Korea Canc Ctr Hosp, Dept Pediat, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Lee, Jun Ah
Lee, Soo-Yong
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Korea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Lee, Soo-Yong
Cho, Wan Hyeong
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Korea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Cho, Wan Hyeong
Song, Won Seok
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Korea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Song, Won Seok
Koh, Jae-Soo
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Korea Canc Ctr Hosp, Dept Pathol, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Koh, Jae-Soo
Yoo, Ji Young
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Korea Canc Ctr Hosp, Dept Radiol, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Yoo, Ji Young
Oh, Dong Hyun
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Korea Canc Ctr Hosp, Dept Nucl Med, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Oh, Dong Hyun
Shin, Duk Seop
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Yeungnam Univ, Coll Med, Dept Orthoped Surg, Taegu, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea
Shin, Duk Seop
Jeon, Dae-Geun
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Korea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South KoreaKorea Canc Ctr Hosp, Dept Orthoped Surg, Seoul 139706, South Korea