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. 2019 Feb 20;8(3):953–962. doi: 10.1002/cam4.1973

Table 1.

Patient characteristics

Characteristics Training cohort
No. (%)
Validation cohort
No. (%)
P value
Sex (male/female) 31/33 44/42 0.512
Age (median y, range) 74 (33‐86) 71 (24‐90) 0.019
ECOG Performance status <0.01
0, 1 45 (70) 81 (94)
≥2 19 (30) 5 (6)
Stage <0.01
I, II 12 (19) 54 (63)
III 13 (20) 11 (13)
IV 39 (61) 21 (24)
Extranodal sites 0.281
0 33 (34) 60 (70)
≥1 42 (66) 26 (30)
Bone marrow involvement 0.541
Yes 11 (17) 10 (12)
No 53 (83) 76 (88)
B symptoms 0.330
Yes 29 (58) 12 (14)
No 35 (42) 74 (86)
LDH 0.285
≤Normal 21 (33) 45 (52)
≥Normal 43 (67) 41 (48)
sIL‐2R 0.409
Median (range) 1735 (243‐43 700) U/mL 1274 (200‐39 798) U/mL
<1300 27 (42) 40 (47)
≥1300 37 (58) 46 (53)
TMTV 0.411
Median (range) 236.32 (76.62‐677.09) cm3 167.2305 (4.61‐5445.50) cm3
<150 26 (41) 44 (51)
≥150 38 (59) 42 (49)
NCCN‐IPI 0.014
Low, Low‐int 15 (24) 47 (55)
High‐int 20 (31) 33 (38)
High 29 (45) 6 (7)
Treatment <0.01
R‐CHOP 27(42) 81(94)
R‐THP‐COP 36(56) 5(6)
R‐CVP 1(2) 0(0)
Outcome
CR 42 (66) 69 (80) 0.0594
PR 7(11) 2(2) 0.0378
Residual disease 18 (28) 18 (21) 0.338
Relapse 16 (25) 14 (16) 0.218
Death from disease 12 (19) 5 (6) 0.0184
Treatment‐related death 11 (17) 8 (9) 0.214
Death from other reasons 5 (8) 2 (2) 0.134

CR, complete remission; ECOG, Eastern Cooperative Oncology Group; LDH, lactate dehydrogenase; NCCN‐IPI, National Comprehensive Cancer Network‐International Prognostic Index; PR, partial remission; residual disease includes the patient with PR, stable disease, and progressive disease.; R‐CHOP, rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone; R‐CVP, rituximab, cyclophosphamide, vincristine, and prednisolone; R‐THP‐COP, rituximab, therarubicin, cyclophosphamide, vincristine, and prednisone; sIL‐2R, soluble interleukin‐2 receptor; TMTV, total metabolic tumor volume.