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. 2013 Mar 8;92(7):925–933. doi: 10.1007/s00277-013-1716-2

Table 3.

Univariate analysis of prognostic factors associated with overall survival and progression-free survival

Group No. 5-year OS (95 % CI) p value 5-year PFS (95 %) p value
Ann Arbor stage
I–II 14 84.6 (57.8–95.7) 0.099 78.6 (52.3–92.5) 0.10
III–IV 50 53.0 (36.5–68.8) 52.1 (36.8–67.0)
B symptoms at diagnosis
No 14 83.3 (55.1–95.3) 0.066 85.1 (58.8–95.8) 0.023
Yes 51 53.8 (37.3–69.5) 51.5 (36.6–66.2)
Bone marrow involvement at diagnosis
No 44 69.2 (50.9–82.9) 0.004 69.9 (53.7–82.3) 0.002
Yes 16 34.9 (15.1–61.9) 24.1 (8.8–51.1)
Response to induction regimen
≥PR 53 66.0 (49.9–79.1) 0.050 65.2 (50.0–77.8) 0.004
Primary refractorinessa 12 41.0 (16.6–70.9) 33.3 (6.6–60.0)
Disease status at transplant
CR 36 65.7 (46.9–80.6) 0.46 64.5 (46.3–79.3) 0.23
less than CR 29 57.1 (35.5–76.3) 54.7 (36.5–72.9)
Number of prior chemotherapy regimen
1 19 77.2 (53.7–90.7) 0.17 78.7 (56.6–90.8) 0.08
2 or more 46 56.8 (40.7–71.6) 51.7 (36.9–66.2)
Histology
ALK-positive and ALK-unknown ALCL 13 54.2 (26.2–79.8) 0.70 59.8 (33.4–81.5) 0.89
Other types 52 63.3 (47.1–77.0) 59.3 (44.4–72.6)
ALCL-all subtypes 20 63.6 (38.8–82.8) 0.77 63.8 (41.7–81.3) 0.70
PTCL-NOS and AITL 45 60.7 (43.4–75.7) 57.5 (41.5–72.1)
ALK-positive and ALK-unknown ALCL 13 54.2 (26.2–79.8) 0.74 59.8 (33.4–81.5) 0.62
ALK-negative ALCL 7 83.3 (43.7–97.0) 71.4 (35.8–91.8)
PTCL-NOS 36 60.7 (42.3–76.5) 55.8 (39.0–71.3)
AITL 9 55.6 (18.0–87.7) 55.6 (18.0–87.7)

OS overall survival, PFS progression-free survival, CI confidence interval, CR complete response, PR partial response, ALK anaplastic lymphoma kinase, ALCL anaplastic large cell lymphoma, PTCL peripheral T cell lymphoma, NOS not otherwise specified, AITL angioimmunoblastic T cell lymphoma

aLess than PR