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