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. 2023 Apr 25;7(17):5172–5186. doi: 10.1182/bloodadvances.2023009953

Table 3.

Variables correlating with inferior OS in the CCD cohort (n = 87)


Variable
n (%) Univariate analysis
Multivariate analysis
HR 95% CI P HR 95% CI P
Age > 60 y 50 (57) 1.3 0.6-2.7 .54
Stage III/IV 72 (83) 2.7 0.6-11.4 .18
Performance: ECOG PS ≥ 2 10 (11) 3.6 1.6-8.0 .002 19.2 2.8-133.0 .003
LDH elevated 53 (61) 2.4 1.1-5.7 .04 1.9 0.5-7.2 .33
BM involvement (by morphological assessment) 32 (37) 3.4 1.7-7.0 <.001 3.8 0.8-19.0 .10
Other extranodal sites of involvement 35 (40) 2.1 1.0-4.2 .04 1.0 0.2-4.5 .96
IPI score, n (%)
 0-1 (group 1) 17 (20) 1.0
 2 (group 2) 28 (32) 4.4 0.5-35.0 .16 7.8 0.8-73.0 .07
 3 (group 3) 30 (34) 7.5 1.0-57.0 .052 2.1 0.1-28.0 .59
 4-5 (group 4) 12 (14) 11.8 1.5-95.0 .02 0.4 0.01-21.0 .64
PIT score, n (%)
 0-1 (group 1) 44 (51) 1.0
 2 (group 2) 24 (28) 2.1 0.8-5.2.0 .13 0.8 0.2-3.5 .76
 3-4 (group 3) 19 (22) 4.3 1.8-10.0 <.001 1.3 0.1-30.0 .87
Histology
 PTCL-NOS 28 (32) 1.0
 PTCL-TFH 6 (7) 1.0 0.2-4.3 .95
 AITL 39 (45) 0.8 0.4-1.8 .61
 ALK+ ALCL 2 (2) 0.0 - .99
 ALK ALCL 8 (9) 0.3 0.04-2.4 .26
 MEITL 4 (5) 0.9 0.1-7.1 .93
Use of etoposide-containing regimens 47 (54) 0.7 0.3-1.3 .25
Use of BV-containing regimens 12 (14) 1.9 0.6-6.5 .31
ASCT consolidation 37 (43) 0.2 0.1-0.5 <.001 0.1 0.04-0.40 < .001
Maintenance therapy 12 (14) 0.4 0.1-1.2 .09
TP53 mutation 13 (15) 0.7 0.2-1.9 .45
TP53 or 17p deletion 5 (6) 1.4 0.3-6.0 .63
CDKN2A deletion 7 (8) 5.3 1.9-14.4 .001 12.1 2.8-52.0 < .001
TET2 mutation 48 (55) 1.3 0.6-2.7 .47
DNMT3A mutation 17 (20) 1.6 0.7-3.6 .25
DNMT3A exon 23 mutation 5 (6) 0.0 - .99
RHOA mutation 26 (30) 0.9 0.4-2.0 .79
FAT1 mutation 4 (5) 1.9 0.4-8.1 .40
STAT3 mutation 4 (5) 1.1 0.2-8.5 .90
SETD2 mutation 5 (6) 0.0 - .99
IDH2 mutation 7 (8) 2.0 0.7-5.8 .19
PCLG1 mutation 7 (8) 2.1 0.6-7.2 .22
Total number of aberrancies 87 (100) 1.0 1.0-1.1 .04

ECOG PS, Eastern Cooperative Oncology Group performance status; LDH, lactate dehydrogenase.

Bold indicates P < .05.

Twelve patients received maintenance systemic therapy on a clinical trial either after chemotherapy or after ASCT.