Validation of a Highly Sensitive qPCR Assay for the Detection of Plasma Cell-Free Epstein-Barr Virus DNA in Nasopharyngeal Carcinoma Diagnosis

Author:

Anh Vu Nguyen Quynh1,Van Ba Nguyen2,Anh Do Tram3,Ung Nguyen Dinh1,Hiep Nguyen Hoang1ORCID,Ly Vu Thi1,Hang Dinh Thi Thu4,Sy Bui Tien5,Chinh Hoang Dao6,Ky Le Minh7,Phong Vu Truong7,Luu Nguyen Kim8,Trung Nguyen Thanh9,Son Ho Anh4,Van Luong Hoang4,Thuan Nghiem Duc3,Tung Ngo Thanh10,Tho Ho Huu1ORCID

Affiliation:

1. Department of Genomics and Cytogenetics, Institute of Biomedicine & Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam

2. Oncology Centre, 103 Military Hospital, Vietnam Military Medical University, Hanoi, Vietnam

3. ENT Department, 103 Military Hospital, Vietnam Military Medical University, Hanoi, Vietnam

4. Institute of Biomedicine & Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam

5. Department of Microbiology, 108 Military Central Hospital, Hanoi, Vietnam

6. Department of Oncology and Radiation, 108 Military Central Hospital, Hanoi, Vietnam

7. Oncology and Head & Neck Surgery Centre, Vietnam National ENT Hospital, Hanoi, Vietnam

8. Department of Radiation, 103 Military Hospital, Vietnam Military Medical University, Hanoi, Vietnam

9. HUS High School for Gifted Students, Hanoi, Vietnam

10. Department of Head & Neck Cancer and Radiation Oncology, Vietnam National K Hospital, Hanoi, Vietnam

Abstract

Quantification of plasma cell-free Epstein Barr virus DNA (cf EBV DNA) has been suggested as a promising liquid biopsy assay for screening and early detection of nasopharyngeal carcinoma (NPC). However, the diagnostic value of this assay is currently not known in the population of Vietnam, one of the countries which contributed the most to the NPC cases. Herein, we have reported a highly sensitive quantitative polymerase chain reaction (qPCR)-based assay targeting cf EBV DNA for the detection of NPC. A standard curve with linear regression, R 2 = 0.9961 (range: 25-150 000 copies/mL) and a detection limit of 25 copies/mL were obtained using an EBV standard panel provided by the Chinese University of Hong Kong. The clinical performance of this assay was assessed using plasma samples obtained from 261 Vietnamese individuals. The optimized qPCR assay detected cf EBV DNA in plasma with a sensitivity of 97.4% and a specificity of 98.2%. The absolute quantitative results of pretreatment cf EBV DNA and patient overall clinical stages were statistically correlated ( P < .05). In summary, the remarkably high sensitivity and specificity of our optimized qPCR assay strongly supports the wide use of cf EBV DNA quantification as a routine noninvasive method in early diagnosis and management of patients with NPC.

Funder

Hanoi Department of Science and Technology

Publisher

SAGE Publications

Subject

Oncology,Hematology,General Medicine

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