Influence of cell proportions and proliferation rates on FDG uptake in squamous-cell esophageal carcinoma: A PET study

被引:6
作者
Buchmann, Inga [1 ,2 ]
Haberkorn, Uwe [1 ]
Schmidtmann, Irene [3 ]
Brochhausen, Christoph [4 ]
Buchholz, Hans-Georg [2 ]
Bartenstein, Peter [2 ]
Hansen, Torsten [4 ,5 ]
机构
[1] Univ Kliniken Heidelberg, Abt Nukl Med, Heidelberg, Germany
[2] Univ Kliniken Mainz, Nukl Med Klin & Poliklin, Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Inst Med Biostat Epidemiol & Informat, D-6500 Mainz, Germany
[4] Univ Kliniken Mainz, Inst Pathol, Mainz, Germany
[5] Univ Kliniken Jena, Inst Pathol, Jena, Germany
关键词
carcinoma of the esophagus; ki-67; staining; fluoro-2-deoxy-glucose PET; quantitative FDG uptake; proliferation activity;
D O I
10.1089/cbr.2007.349
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We investigated the influence of cell proportions and proliferation activities on tumor maximum standard uptake value (SUV(max)) in patients with squamous-cell esophageal cancer (SCEC). Methods: Sixteen (16) patients with untreated SCEC were examined with (18)F-flourodeoxyglucose positron emission tomography (FDG-PET). The tumor SUV(max) were calculated. Tumors were resected by transthoracic esophagectomy. Tissues were stained with hematoxylin and eosin for the measurement of cell proportions and MIB-1 for measurement of proliferation indices (PIs). Tumor SUV and histologic data were related by using multiple linear regression analysis. Results: The mean proportion of tumor cells in the tumor site was 58.1% (+/- 12.1%); the proportion of inflammatory cells was 34.2% (+/- 14.2%); the PI of tumor cells was 70.5% (+/- 11.8%); and the PI of inflammatory cells was 22.2% (+/- 7.6%). The tumor PI was the only variable that was significantly associated with the FDG uptake in the tumor site (p=0.04). The correlation was low (Pearson-coefficient Gamma=0.51). The Pearson-correlation-coefficient between tumor SUV and the fraction of inflammatory cells was Gamma=0.37 and between tumor SUV and PI of inflammatory cells Gamma=0.13. Conclusions: In untreated SCEC-patients, the tumor maximum FDG uptake is weakly associated with the proliferation rate of tumor cells. In contrast, neither the proportion nor the PI of inflammatory cells in the tumor site significantly correlates with the maximum SUV and should not profoundly affect PET interpretations.
引用
收藏
页码:172 / 180
页数:9
相关论文
共 33 条
[1]  
Avril N, 2001, J NUCL MED, V42, P9
[2]  
BEAHRS OH, 1998, MANUAL STAGING CANC, P63
[3]   Biologic correlates of 18fluorodeoxyglucose uptake in human breast cancer measured by positron emission tomography [J].
Bos, R ;
van der Hoeven, JJM ;
van der Wall, E ;
van der Groep, P ;
van Diest, PJ ;
Comans, EFI ;
Joshi, U ;
Semenza, GL ;
Hoekstra, OS ;
Lammertsma, AA ;
Molthoff, CFM .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (02) :379-387
[4]  
Buchmann I, 2006, NUKLEARMED-NUCL MED, V45, P235
[5]  
Buchmann I, 2004, CANCER BIOTHER RADIO, V19, P436
[6]  
Chino O, 1998, J SURG ONCOL, V67, P18, DOI 10.1002/(SICI)1096-9098(199801)67:1<18::AID-JSO4>3.0.CO
[7]  
2-P
[8]  
CREMERIUS U, 1994, NUKLEARMED, V33, P144
[9]   Uptake of [18F]fluorodeoxyglucose in human monocyte-macrophages in vitro [J].
Deichen, JT ;
Prante, O ;
Gack, M ;
Schmiedehausen, K ;
Kuwert, T .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2003, 30 (02) :267-273
[10]   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