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Table 1 Clinicopathologic features of rituximab-treated diffuse large B cell lymphoma patients (N = 103)

From: Overexpression of sphingosine-1-phosphate receptor 1 and phospho-signal transducer and activator of transcription 3 is associated with poor prognosis in rituximab-treated diffuse large B-cell lymphomas

Variables

Total n (%)

GCB*n (%)

Non-GCB*n (%)

Age, years

   

 Mean (range)

57.7 (14–79)

60.5 (23–79)

56.2 (14–78)

 <60

50 (49%)

13 (35%)

35 (56%)

 ≥60

53 (51%)

24 (65%)

27 (44%)

Sex

   

 Male

61 (59%)

23 (62%)

36 (58%)

 Female

42 (41%)

14 (38%)

26 (42%)

Primary site

   

 Nodal

37 (36%)

14 (38%)

21 (34%)

 Extranodal

66 (64%)

23 (62%)

41 (66%)

Ann Arbor stage

   

 I, II

47 (46%)

19 (51%)

27 (44%)

 III, IV

56 (54%)

18 (49%)

35 (56%)

IPI group†

   

 Low (0–2)

60 (63%)

24 (65%)

33 (60%)

 High (3–5)

36 (37%)

13 (35%)

22 (40%)

B symptoms†

   

 Absent

74 (76%)

31 (84%)

43 (72%)

 Present

24 (24%)

6 (16%)

17 (28%)

ECOG PS†

   

 0, 1

86 (84%)

34 (92%)

49 (80%)

 ≥2

16 (16%)

3 (8%)

12 (20%)

LDH†

   

 Normal

43 (45%)

14 (39%)

26 (46%)

 Elevated

53 (55%)

22 (61%)

30 (54%)

BM involvement†

   

 Absent

85 (86%)

34 (92%)

48 (83%)

 Present

14 (14%)

3 (8%)

10 (17%)

Number of extranodal sites

   

 0, 1

75 (73%)

26 (70%)

46 (74%)

 ≥2

28 (27%)

11 (30%)

16 (26%)

EBER†

   

 Negative

95 (94%)

37 (100%)

55 (90%)

 Positive

6 (6%)

0 (0%)

6 (10%)

Treatment

   

 Rituximab + CHOP

97 (94%)

37 (100%)

57 (92%)

 Rituximab + others

6 (6%)

0 (%)

5 (8%)

  1. GCB, germinal center B-cell like; IPI, international prognostic index; ECOG PS, Eastern Cooperative Oncology Group performance status; LDH, lactate dehydrogenase; BM, bone marrow; EBER, EBV-encoded RNA; CHOP, cyclophosphamide, doxorubicin, vincristine, prednisolone. *GCB and non-GCB phenotypes were classified using Hans classification with four unclassifiable cases. †The number excludes missing values.