Clinical significance of plasma Epstein-Barr Virus DNA loads in a large cohort of Malaysian patients with nasopharyngeal carcinoma

被引:47
作者
Chai, San Jiun [3 ]
Pua, Kin Choo [4 ]
Saleh, Amyza [3 ]
Yap, Yoke Yeow [5 ]
Lim, Paul V. H. [6 ]
Subramaniam, Selva Kumar [7 ]
Lum, Chee Lun [8 ]
Krishnan, Gopala [9 ]
Mahiyuddin, Wan Rozita Wan [10 ]
Teo, Soo-Hwang [3 ]
Khoo, Alan S. B. [11 ]
Yap, Lee Fah [1 ,2 ,3 ]
机构
[1] Univ Malaya, Dent Res & Training Unit, Fac Dent, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Oral Canc Res & Coordinating Ctr, Fac Dent, Kuala Lumpur 50603, Malaysia
[3] Canc Res Initiat Fdn, Subang Jaya, Malaysia
[4] Hosp Pulau Pinang, Dept Otorhinolaryngol, George Town, Malaysia
[5] Univ Putra Malaysia, Hosp Kuala Lumpur, Dept Surg, Clin Campus Fac Med & Hlth Sci, Kuala Lumpur, Malaysia
[6] Tung Shin Hosp, ENT Dept, Kuala Lumpur, Malaysia
[7] Sarawak Gen Hosp, Dept Otorhinolaryngol Head & Neck Surg, Sarawak, Malaysia
[8] Queen Elizabeth Hosp, ENT Dept, Sabah, Malaysia
[9] Univ Malaya, Dept Otorhinolaryngol, Fac Med, Kuala Lumpur 50603, Malaysia
[10] Inst Med Res, Epidemiol & Biostat Unit, Kuala Lumpur 50588, Malaysia
[11] Inst Med Res, Mol Pathol Unit, Kuala Lumpur 50588, Malaysia
关键词
Nasopharyngeal carcinoma; Epstein-Barr Virus; Diagnosis; Metastasis; VIRAL CAPSID ANTIGEN; DIAGNOSTIC-VALUE; SERUM; ANTIBODY; IGA; QUANTIFICATION; METASTASIS; SURVIVAL; BLOOD;
D O I
10.1016/j.jcv.2012.05.017
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Nasopharyngeal carcinoma (NPC) is an Epstein-Barr Virus (EBV)-associated cancer that is the fifth most common cancer in Malaysia. Early and accurate diagnoses are critical for patient prognosis. Unfortunately, early detection of NPC is still a challenge and the cost of more accurate imaging protocols is prohibitive in developing countries like Malaysia. Objectives: To evaluate the clinical values of pre-treatment plasma EBV DNA levels in Malaysian NPC patients. Study design: Plasma EBV DNA levels were measured by quantitative PCR (Q-PCR) in a large and multi-ethnic cohort of Malaysian patients with NPC (n = 459) and 72 control subjects. Results: We show for the first time that, compared to controls, NPC patients with stage I disease had significantly higher levels of EBV DNA (p < 0.001). Further, the median level of plasma EBV DNA in stage IV patients with distant metastasis was >9-fold higher than those without systemic spread (p = 0.001), suggesting plasma EBV DNA measurement could aid in the diagnosis of metastatic disease in advanced cases. Further, using a cut-off value of 8000 copies/mL, we demonstrate that EBV DNA level is a strong predictor for overall survival of NPC patients. Conclusions: Our data show that pre-treatment plasma EBV DNA is a potential biomarker for early stage and metastatic NPC. We conclude that the quantification of plasma EBV DNA is a useful tool in developing countries to stratify patients for MRI or PET/CT scans where such imaging protocol is not routinely applied. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:34 / 39
页数:6
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