Relationship between pretreatment level of plasma Epstein-Barr virus DNA, tumor burden, and metabolic activity in advanced nasopharyngeal carcinoma

被引:96
作者
Ma, Brigette B. Y.
King, Ann
Lo, Y. M. Dennis
Yau, Y. Y.
Zee, Benny
Hui, Edwin P.
Leung, Sing F.
Mo, Frankie
Kam, Michael K.
Ahuja, Anil
Kwan, Wing H.
Chan, Anthony T. C. [1 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Sir YK Pao Ctr Canc, Dept Clin Oncol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Diagnost Radiol & Organ Imaging, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Chem Pathol, Shatin, Hong Kong, Peoples R China
[4] Hong Kong Baptist Hosp, PET CT Ctr, Kowloon, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Sch Publ Hlth, Ctr Clin Trials, Hong Kong, Hong Kong, Peoples R China
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2006年 / 66卷 / 03期
关键词
nasopharyngeal carcinoma; plasma Epstein-Barr virus DNA; positron emission tomography; magnetic resonance imaging;
D O I
10.1016/j.ijrobp.2006.05.064
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Plasma Epstein-Barr virus DNA (pEBV DNA) is an important prognostic marker in nasopharyngeal carcinoma (NFC). This study tested the hypotheses that pEBV DNA reflects tumor burden and metabolic activity by evaluating its relationship with tumor volume and F-18-fluorodeoxyglucose (F-18-FDG) uptake in NPC. Methods and Materials: Pre-treatment pEBV DNA analysis, F-18-FDG positron emission tomography-computed tomography scan (PET-CT) and magnetic resonance imaging (MRI) of the head and neck were performed in 57 patients. Net volume (cm(3)) of the primary tumor (T-vol) and regional nodes (N-vol)were quantified on MRI. F-18-FDG uptake was expressed as the maximum standardized uptake value (SUVmax) at the primary tumor (T-suv) and regional nodes (N-suv). Lesions with SUVmax >= 2.5 were considered malignant. Relationship between SUVmax, natural logarithm (log) of pEBV DNA, and square root (sq) of MRI volumes was analyzed using the Wilcoxon test. A linear regression model was constructed to test for any interaction between variables and disease stage. Results: Log-pEBV DNA showed significant correlation with sq-T-vol (r = 0.393), sq-N-vol (r = 0.452), total tumor volume (sq-Total(vol) = T-vol + N-vol, r = 0.554), T-suv (r = 0.276), N-suv (r = 0.434), and total SUVmax. (Total(suv) = T-suv + N-suv, r = 0.457). Likewise, sq-T-vol, was correlated to T-suv (r = 0.426), and sq-N-vol with N-suv (r = 0.651). Regression analysis showed that only log-pEBV DNA was significantly associated with sq-Total(vol) (p < 0.001; parameter estimate = 8.844; 95% confidence interval = 3.986-13.703), whereas Sq-T-vol was significantly associated with T-suv (p = 0.002; parameter estimate = 3.923; 95% confidence interval = 1.498-6.348). Conclusion: This study supports the hypothesis that cell-free plasma EBV DNA is a marker of tumor burden in EBV-related NPC. (c) 2006 Elsevier Inc.
引用
收藏
页码:714 / 720
页数:7
相关论文
共 42 条
[1]  
AJCC, 2002, CANC STAG HDB
[2]   Accuracy of whole-body dual-modality fluorine-18-2-fluoro-2-deoxy-D-glucose positron emission tomography and computed tomography (FDG-PET/CT) for tumor staging in solid tumors: Comparison with CT and PET [J].
Antoch, G ;
Saoudi, N ;
Kuehl, H ;
Dahmen, G ;
Mueller, SP ;
Beyer, T ;
Bockisch, A ;
Debatin, JF ;
Freudenberg, LS .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (21) :4357-4368
[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]   Biological characterisation of breast cancer by means of PET [J].
Buck, AK ;
Schirrmeister, H ;
Mattfeldt, T ;
Reske, SN .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2004, 31 (Suppl 1) :S80-S87
[5]  
CHAN A, 2005, P AM SOC CLIN ONC
[6]  
Chan AT, 2004, J CLIN ONCOL, V22, p493S
[7]  
Chan ATC, 2002, JNCI-J NATL CANCER I, V94, P1614, DOI 10.1093/jnci/94.21.1614
[8]   Investigation into the origin and tumoral mass correlation of plasma Epstein-Barr virus DNA in nasopharyngeal carcinoma [J].
Chan, KCA ;
Chan, ATC ;
Leung, SF ;
Pang, JCS ;
Wang, AYM ;
Tong, JHM ;
To, KF ;
Chan, LYS ;
Tam, LLS ;
Chung, NYF ;
Zhang, J ;
Lo, KW ;
Huang, DP ;
Lo, YMD .
CLINICAL CHEMISTRY, 2005, 51 (11) :2192-2195
[9]  
Chan KCA, 2003, CANCER RES, V63, P2028
[10]   Volumetric analysis of tumor extent in nasopharyngeal carcinoma and correlation with treatment outcome [J].
Chua, DTT ;
Sham, JST ;
Kwong, DLW ;
Tai, KS ;
Wu, PM ;
Lo, M ;
Yung, A ;
Choy, D ;
Leong, L .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1997, 39 (03) :711-719