Positron emission tomography evaluation of residual radiographic abnormalities in postchemotherapy germ cell tumor patients

被引:119
作者
Stephens, AW
Gonin, R
Hutchins, GD
Einhorn, LH
机构
[1] INDIANA UNIV,MED CTR,DEPT RADIOL,DIV IMAGING SCI,INDIANAPOLIS,IN 46204
[2] INDIANA UNIV,MED CTR,DEPT MED,DIV HEMATOL ONCOL,INDIANAPOLIS,IN 46204
[3] INDIANA UNIV,SCH MED,DEPT MED,DIV BIOSTAT,INDIANAPOLIS,IN 46204
关键词
D O I
10.1200/JCO.1996.14.5.1637
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study was performed to assess the ability of positron emission tomography (PET) to differentiate residual radiographic abnormalities in postchemotherapy nonseminomatous germ cell tumor (GCT) patients. Materials and Methods: Thirty patients with nonseminomatous GCT were evaluated with PET scans before surgical resection of a residual mass or masses, Standardized uptake values (SUV) were calculated for the region of maximal 2-fluoro-2-deoxyglucose (FDG) uptake and compared with histologic findings. Results: Eleven patients had necrosis/fibrosis in the resected specimen, 15 had teratoma, and four viable GCT, The median SUV for the necrosis/fibrosis group was 2.86, teratoma 3.07, and viable GCT 8.81. A significant association between SUV and histology was found when comparing viable GCT versus necrosis/fibrosis plus teratoma (P = .004). Patients with an SUV greater than 5 were 75 times more likely to have viable cancer than teratoma or necrosis/fibrosis (odds ratio; 95% confidence interval, 3.66 to 1,536), PET did not differentiate necrosis/fibrosis from teratoma, However, PET was able to differentiate viable GCT from residual necrosis/fibrosis or teratoma. Conclusion: PET-FDG imaging can be useful for detection of residual viable carcinoma following chemotherapy in nonseminomatous GCT patients with residual masses, It may be a valuable adjunct in the determination of which patients should undergo postchemotherapy resection. (C) 1996 by American Society of Clinical Oncology.
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页码:1637 / 1641
页数:5
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