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. Author manuscript; available in PMC: 2018 Oct 1.
Published in final edited form as: Br J Haematol. 2017 Jun 27;179(1):50–60. doi: 10.1111/bjh.14813

Table I.

Patient characteristics at diagnosis

Characteristic All (N=1039) Relapsed (N=250)

Median age (range), years 62 (18–92) 61 (19–89)

Age at diagnosis
  <60 years 475 (46%) 114 (46%)
  >60 years 564 (54%) 136 (54%)

Sex
  Male 577 (56%) 157 (63%)
  Female 462 (44%) 93 (37%)

Histology at diagnosis

DLBCL 983 (95%) 241 (96%)

PMBL 56 (5%) 9 (4%)

IPI at diagnosis

0–1 349 (34%) 47 (19%)

2 305 (29%) 69 (28%)

3 251 (24%) 93 (37%)

4 or 5 134 (13%) 41 (16%)

Stage at diagnosis
I/II 382 (37%) 54 (22%)
III/IV 647 (63%) 194 (78%)

LDH at diagnosis
  >Upper limit of normal 393 (42%) 161 (75%)
  <Upper limit of normal 543 (58%) 55 (25%)

2 or more Extranodal sites at diagnosis
      Yes 215 (21%) 60 (24%)
      No 824 (79%) 190 (76%)

ECOG performance status at diagnosis
  0–1 857 (83%) 186 (75%)
  2–4 179 (17%) 63 (25%)

Any B symptoms at diagnosis
    Yes 256 (25%) 84 (34%)
    No 783 (75%) 166 (66%)

Bulky disease > 10 cm at diagnosis
  Yes 127 (12%) 45 (18%)
  No 912 (88%) 205 (82%)

Bone marrow involvement with DLBCL at diagnosis
      Yes 102 (10%) 33 (13%)
      No 937 (90%) 217 (87%)

Cell of origin (Hans)
  GCB 375 (64%) 74 (59%)
  Non-GCB 210 (36%) 51 (41%)

CNS involvement at diagnosis
  Yes 18 (2%) 8 (3%)
  No 1021 (98%) 242 (97%)

Creatinine at diagnosis 0.9 (0.4–19.1) 1.0 (0.4–4.4)

CNS, central nervous system; DLBCL, diffuse large B cell lymphoma; ECOG, Eastern Cooperative Oncology Group; GCB, germinal centre B cell-like; IPI, International Prognostic Index; LDH, lactate dehydrogenase; PMBL, primary mediastinal B cell lymphoma.