Positron emission tomography/computerized tomography functional imaging of esophageal and colorectal cancer

被引:19
作者
Larson, SM [1 ]
Schoder, H [1 ]
Yeung, H [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, Sloan Kettering Inst, New York, NY 10021 USA
关键词
positron emission tomography; computed tomography; PET/FDG imaging;
D O I
10.1097/00130404-200407000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Positron Emission Tomography/Computerized Emission Tomography (PET/CT) creates fusion images which are a combination of tissue function (PET) and anatomy (CT). PET/CT imaging for esophageal and colorectal cancers improves staging, detection of recurrence, and treatment monitoring. Both tumor types are highly metabolically active in the untreated state, and the glucose analog, 2-[18F]-2-fluoro-2-deoxy-D-glcuose, (FDG), is widely useful as a PET imaging tracer for these malignancies, For esophageal and colorectal malignancies, diagnostic imaging sensitivity and specificity are greater than 90%. For esophageal tumors, PET imaging is standard of care for staging of locally advanced tumor. Fifteen to 20% of patients will have otherwise occult metastatic sites detected by PET imaging at initial staging. Progression free survival and survival are correlated with the magnitude of reduction in PET-FDG measured metabolic activity post-treatment. For colorectal cancers, PET-FDG is standard of care to detect recurrence, and to monitor treatment response. The addition of CT to the PET imaging, causes a significant reduction in uncertainty of image interpretation and improves the distinction between benign and malignant causes for FDG-PET positive sites.
引用
收藏
页码:243 / 250
页数:8
相关论文
共 32 条
[1]  
Beyer T, 2000, J NUCL MED, V41, P1369
[2]  
Brücher BLDM, 2001, ANN SURG, V233, P300
[3]  
Cohade C, 2003, J NUCL MED, V44, P1797
[4]  
Coleman R Edward, 1998, Clin Positron Imaging, V1, P15, DOI 10.1016/S1095-0397(97)00004-6
[5]  
Dietlein M, 2003, NUKLEARMED-NUCL MED, V42, P145
[6]   Whole body 18FDG-PET and the response of esophageal cancer to induction therapy:: Results of a prospective trial [J].
Downey, RJ ;
Akhurst, T ;
Ilson, D ;
Ginsberg, R ;
Bains, MS ;
Gonen, M ;
Koong, H ;
Gollub, M ;
Minsky, BD ;
Zakowski, M ;
Turnbull, A ;
Larson, SM ;
Rusch, V .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (03) :428-432
[7]   Utility of positron emission tomography for the staging of patients with potentially operable esophageal carcinoma [J].
Flamen, P ;
Lerut, A ;
Van Cutsem, E ;
De Wever, W ;
Peeters, M ;
Stroobants, S ;
Dupont, P ;
Bormans, G ;
Hiele, M ;
De Leyn, P ;
Van Raemdonck, D ;
Coosemans, W ;
Ectors, N ;
Haustermans, K ;
Mortelmans, L .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (18) :3202-3210
[8]   Staging of esophageal cancer with F-18-fluorodeoxyglucose positron emission tomography [J].
Flanagan, FL ;
Dehdashti, F ;
Siegel, BA ;
Trask, DD ;
Sundaresan, SR ;
Patterson, GA ;
Cooper, DJ .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1997, 168 (02) :417-424
[9]  
Fong Y, 2000, Adv Surg, V34, P351
[10]   Utility of 18F-FDG positron emission tomography scanning on selection of patients for resection of hepatic colorectal metastases [J].
Fong, YM ;
Saldinger, PF ;
Akhurst, T ;
Macapinlac, H ;
Yeung, H ;
Finn, RD ;
Cohen, A ;
Kemeny, N ;
Blumgart, LH ;
Larson, SM .
AMERICAN JOURNAL OF SURGERY, 1999, 178 (04) :282-287