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Table 3 Clinical application of EBV DNA in T cell lymphoma

From: Liquid biopsy in T-cell lymphoma: biomarker detection techniques and clinical application

Lymphoma subtypes

Author

PMID/doi

Biomarker

Liquid Biopsy

Method

No. of patients

Results

Clinical applications

ENKTL

Lei, Kenny I K et al. [132]

11801537

EBV DNA levels

PB

qRT-PCR

18

plasma EBV DNA was detected in 17/18 patients but in 0/35 control subjects (P < 0.0001)

Clinically responding patients plasma EBV DNA levels fall whereas no responding patients rapid increase

patients baseline plasma EBV DNA levels ≥ 600 copies/ml vs < 600 copies/ml, OS 21% vs 78%; P = 0.024

diagnosis, prognosis. longitudinal monitoring

ENKTL, nTFHL-AI

Au, Wing-Yan et al. [133]

15031209

EBV DNA levels

PB

Q-PCR

39

high-presentation EBV DNA (> 6.1 × 107 copies/mL) was significantly associated with an inferior DFS. During treatment, patients with EBV DNA had significantly inferior OS

diagnosis, prognosis. longitudinal monitoring

ENKTL

Kwong YL et al. [134]

23842425

EBV DNA levels

PB

Q-PCR

56

negative EBV DNA after SMILE had the most significant impact (P < 0.001) on OS and persistently undetectable EBV DNA had the most significant impact (P = 0.002) on DFS

prognosis

ENKTL

Wang XX et al. [135]

30646796

EBV DNA levels

PB

qRT-PCR

99

3-year OS:

pre-, interim-, post-treatment EBV-DNA, positive vs negative, 70.2% vs. 93.9% (P = 0.022), 53.8% vs. 99.1% (P < 0.001), 40.6% vs. 91.8% (P < 0.001)

prognosis. longitudinal monitoring

PTCL, NOS, ALCL, nTFHL-AI

Zhao D et al. [136]

34753127

EBV DNA levels

PB

qRT-PCR

128

pre-treatment EBV-DNA ≥ 500 copies/mL(3-year PFS: 12.2% vs. 48.2%, p = 0.001; 3-year OS: 42.5% vs. 66.1%, P = 0.003)

EBV-DNA with normalization of after first-line chemotherapy ORR (81.3% vs. 22.2%, P = 0.014), PFS (12.0 m vs. 3.7 m, P = 0.011), OS (37.9 m vs. 7.8 m, P = 0.012)

prognosis. longitudinal monitoring

PTCL, NOS, nTFHL-AI, ENKTL

Suwiwat, Supaporn et al. [137]

17996493

EBV DNA levels

PB

RT-PCR

45

concentration of EBV DNA in the plasma was not a prognostic marker in PTCL and PTPD patients

prognosis

nTFHL-AI

Delfau-Larue, MH et al. [138]

22371178

EBV DNA levels

PB

RT-PCR

25

peripheral EBV load at diagnosis (≥ 100 copy/μg DNA) was associated with shorter PFS (P = 0.06)

prognosis

ENKTL

Wang ZY et al. [139]

22826562

EBV DNA levels

PB

RT-PCR

69

3-year OS and PFS rates: pretreatment EBV-DNA level of ≤ 500 copies/mL vs > 500 copies/mL, 97.1% and 79.0% vs 66.3% (P = .002) and 52.2% (P = .045)

prognosis

ENKTL

Wang L et al. [140]

26210287

EBV DNA levels

PB

qRT-PCR

68

Patients with negative pretreatment EBV-DNA had a higher CR rate (96.0% vs. 69.8%, P = 0.023)

post-treatment EBV-DNA positivity and treatment response (non-CR) were prognostic factors for both worse PFS and OS (P < 0.05)

prognosis

MRD

  1. EBV Epstein-Barr virus, EBV DNA Epstein-Barr virus DNA, ENKTL extranodal NK/T-cell lymphoma, PTCL, NOS peripheral T-cell lymphoma, not otherwise specified, nTFHL-AI Nodal T-follicular helper cell lymphoma, angioimmunoblastic-type, PTPD peripheral T-cell proliferative diseases, qRT-PCR real-time quantitative PCR, OS overall survival, DFS disease-free survival, PFS progression-free survival