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Table 1 Correlation between TMB and clinical phenotype for 59-Brazilian patients with nMTCL

From: Tumor mutation burden involving epigenetic regulatory genes and the RhoA GTPase predicts overall survival in nodal mature T-cell lymphomas

Characteristic

Low-TMB (N, %) (48/59–81.3%)

High-TMB (N, %) (11/59–18.7%)

p value

Male gender

25 (52.1%)

09 (81.8%)

p = 0.06

IPI ≥ 3 points

26 (54.2%)

07 (63.6%)

p = 0.56

PIT ≥ 3 points

23 (47.9%)

07 (63.6%)

p = 0.34

ECOG ≥ 2

25 (52.1%)

08 (72.8%)

p = 0.21

Bulky disease ≥ 7 cm

26 (54.2%)

10 (90.9%)

p = 0.01

B-symptoms

39 (81.3%)

10 (90.9%)

p = 0.41

BM infiltration

05 (10.4%)

02 (18.2%)

p = 0.78

≥ 2 extra nodal sites

13 (27.1%)

03 (27.3%)

p = 0.87

Clinical stage III/IV

45 (93.8%)

11 (100%)

p = 0.75

ORR

29 (60.4%)

04 (36.4%)

p = 0.08

Mortality

23 (47.9%)

09 (81.8%)

p = 0.04

  1. TMB tumor mutation burden, IPI international prognostic index, PIT prognostic index for peripheral T-cell lymphomas, ECOG Eastern Cooperative Oncology Group, BM bone marrow, ORR overall mortality rate