[18F]fluorodeoxyglucose positron emission tomography is more sensitive than skeletal scintigraphy for detecting bone metastasis in endemic nasopharyngeal carcinoma at initial staging

被引:83
作者
Liu, FY
Chang, JT
Wang, HM
Liao, CT
Kang, CJ
Ng, SK
Chan, SC
Yen, TC
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Dept Nucl Med, Taipei 10507, Taiwan
[2] Chang Gung Univ, Chang Gung Mem Hosp, Mol Imaging Ctr, Taipei 10507, Taiwan
[3] Chang Gung Univ, Chang Gung Mem Hosp, Dept Radiat Oncol, Div Hematol Oncol, Taipei 10507, Taiwan
[4] Chang Gung Univ, Chang Gung Mem Hosp, Dept Internal Med, Sect Head & Neck Surg, Taipei 10507, Taiwan
[5] Chang Gung Univ, Chang Gung Mem Hosp, Dept Otorhinolaryngol, Taipei 10507, Taiwan
[6] Chang Gung Univ, Chang Gung Mem Hosp, Dept Diagnost Radiol, Taipei 10507, Taiwan
关键词
D O I
10.1200/JCO.2005.03.8760
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Bone metastasis occurs frequently in patients with endemic nasopharyngeal carcinoma (NPC). The main objective of this study is to evaluate positron emission tomography (PET) using fluorine-18-labeled fluorodeoxyglucose ([F-18]FDG) and conventional skeletal scintigraphy (SS) for detecting bone metastasis at initial staging. Auxiliary objectives are to identify risk factors for bone metastasis and features associated with poor survival in patients with bone metastasis. Patients and Methods Patients with endemic NPC before initiation of treatment were enrolled. PET and SS were performed at initial staging and compared using McNemar's paired-sample test. Bone metastasis was considered to be present if there was any reliable evidence identified within I year after primary diagnosis. Multiple logistic regression and Cox's proportional hazards models were used for auxiliary objectives. Results Thirty (15%) of 202 eligible patients were found to have bone metastasis. [F-18]FDG PET was found to be more sensitive than SS in the patient-based analysis (P = .006) and in the region-based analysis at the spine (P = .001). Advanced N stage was the only significant risk factor (P < .0001), and the coexistence of hepatic metastasis was a prognosticator of poor survival (P = .017). The survival was not significantly better for patients with bone metastasis Undetected at primary staging than for those with initially detectable bone metastasis (P = .620). Conclusion [F-18]FDG PET is more sensitive than SS for detecting bone metastasis in endemic NPC at initial staging, whereas SS can be considered as supplementary in this setting.
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收藏
页码:599 / 604
页数:6
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