Positron emission tomography in limited-stage small-cell lung cancer: A prospective study

被引:190
作者
Bradley, JD
Dehdashti, F
Mintun, MA
Govindan, R
Trinkaus, K
Siegel, BA
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Radiol, Mallinckrodt Inst Radiol,Dept Biostat, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, St Louis, MO 63110 USA
关键词
D O I
10.1200/JCO.2004.11.089
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine how often positron emission tomography with [F-18]fluoro-2-deoxy-D-glucose (FDG-PET) detects extensive-stage small-cell lung cancer (SCLC) in patients considered to have limited-stage disease based on conventional staging procedures, and to determine the impact of PET on treatment planning for presumed limited-stage SCLC. Patients and Methods We prospectively performed pretreatment FDG-PET on 24 patients determined by conventional staging methods to have limited-stage SCLC (defined as disease that could be encompassed within a reasonable radiotherapy portal, excluding bilateral supraclavicular disease). PET images were evaluated for evidence of extensive-stage disease. Tumor-node-metastasis system staging was also assigned for each patient, with and without PET information. Results FDG-PET demonstrated findings consistent with extensive-stage SCLC in three of 24 patients. FDG-PET correctly upstaged two (8.3%) of 24 patients to extensive-stage disease (95% CI, 1.03% to 27.0%). PET correctly identified tumor in each SCLC mass (primary or nodal) that was suspected on computed tomography (CT) imaging, thus giving a lesion-based sensitivity relative to CT of 100%. PET identified unsuspected regional nodal metastasis in six (25%) of 24 patients, and the radiation therapy plan was significantly altered to include the PET-positive/CT-negative nodes within the high-dose region in each of these patients. Brain PET images in 23 patients disclosed no evidence of brain metastasis. Conclusion FDG-PET has high sensitivity for SCLC and appears to be of value for initial staging and treatment planning of patients with presumed limited-stage disease. (C) 2004 by American Society of Clinical Oncology.
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页码:3248 / 3254
页数:7
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