Prospective measurement of Epstein-Barr virus–DNA in plasma and peripheral blood mononuclear cells of extranodal NK/T-cell lymphoma, nasal type

Author:

Suzuki Ritsuro1,Yamaguchi Motoko2,Izutsu Koji3,Yamamoto Go3,Takada Kenzo4,Harabuchi Yasuaki5,Isobe Yasushi6,Gomyo Hiroshi7,Koike Tadashi8,Okamoto Masataka9,Hyo Rie1,Suzumiya Junji10,Nakamura Shigeo11,Kawa Keisei12,Oshimi Kazuo6,

Affiliation:

1. Department of HSCT Data Management and Biostatistics, Nagoya University Graduate School of Medicine, Nagoya, Japan;

2. Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan;

3. Department of Hematology and Oncology, Tokyo University School of Medicine, Tokyo, Japan;

4. Department of Virology, Hokkaido University Graduate School of Medicine, Sapporo, Japan;

5. Department of Otorhinoraryngology, Asahikawa Medical University, Asahikawa, Japan;

6. Department of Hematology, Juntendo University, Tokyo, Japan;

7. Department of Hematology, Hyogo Cancer Center, Kobe, Japan;

8. Department of Hematology, Nagaoka Red Cross Hospital, Nagaoka, Japan;

9. Department of Hematology, Fujita Health University School of Medicine, Fujita, Japan;

10. Department of Hematology, Fukuoka University School of Medicine, Fukuoka, Japan;

11. Department of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan; and

12. Department of Pediatrics, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan

Abstract

Abstract Epstein-Barr virus (EBV)–DNA was prospectively analyzed in plasma and mononuclear cells (MNCs) from peripheral blood in patients with extranodal natural killer (NK)/T-cell lymphoma, nasal type, to evaluate the clinical significance for diagnosis, monitoring the tumor burden, and prognostication. Thirty-three patients were enrolled, and 32 were evaluable. Pretreatment plasma and MNC EBV-DNA was detectable in 14 (range, 50-71 000 copies/mL) and 6 patients (range, 20-780 copies/μg DNA), respectively, and both were well correlated (r = 0.8741, P < .0001). Detectable plasma EBV-DNA was associated with higher clinical stage (P = .02), presence of B symptoms (P = .02), worse performance status (P = .02), and higher serum soluble IL-2 receptor level (P < .0001). Twenty-two patients attained complete response. Plasma EBV-DNA level was significantly higher in nonresponders than in responders (mean, 16 472 vs 2 645 copies/mL; P = .02). Multivariate analysis showed clinical stage (hazard ratio, 9.0; 95% confidence interval, 1.8%-45.0%) and pretreatment plasma EBV-DNA (hazard ratio, 10.6; 95% confidence interval, 1.3%-87.0%) were significant prognostic factors. Three-year overall survival of plasma EBV-DNA positive and negative patients was 42.9% and 94.4%, respectively (P = .0009). Plasma was a preferable sample for this purpose in NK/T-cell lymphoma, nasal type, and EBV-DNA level was a good indicator for response and overall survival.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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