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. Author manuscript; available in PMC: 2011 Jul 1.
Published in final edited form as: Br J Haematol. 2010 May 9;150(2):170–178. doi: 10.1111/j.1365-2141.2010.08210.x

Table I.

Patients’ Clinical Characteristics

Patient No. Histological Subtype Age (years) Sex Donor Prior Tx (n) Failed Prior ASCT Disease Status Prior to Tx Time from Dx to Tx (months)
1 AITL 51 F MR 5 Yes SD 22
2 PTCL-NOS 61 M MUR 4 Yes CR 29
3 PTCL-NOS 55 M MUR 3 Yes CR 27
4 T-PLL 59 M MUR 3 No PD 25
5 AITL 51 M MUR 6 Yes CR 25
6 PTCL-NOS 61 F MR 8 Yes PR 144
7 PTCL-NOS 25 M MUR 1 No CR 8
8 CTCL-SS 61 M MUR 7 No PD 20
9 AITL 72 M MR 3 No PR 6
10 PTCL-NOS 57 F MUR 4 No PR 21
11 PTCL-NOS 58 M MR 3 No SD 22
12* NKC-L/L 63 M MR 1 No CR 9
13 T-PLL 62 F MR 2 No PR 9
14 T-PLL 59 M MUR 3 No PR 50
15* AITL 57 F MUR 1 No CR 6
16 ALCL 45 M MR 4 Yes CR 48
17* PTCL-NOS 73 M MUR 2 No CR 6

Abbreviations: AITL=angioimmunoblastic T-cell lymphoma; ALCL=anaplastic large cell lymphoma; ASCT=autologous stem cell transplantation; CR=complete remission; MR=matched related; MRD=minimal residual disease; MUR=matched unrelated; NK-L/L=NK-cell leukaemia/lymphoma; PD=progressive disease; PR=partial remission; PTCL-NOS=peripheral T-cell lymphoma, not otherwise specified; CTCL-SS = Cutaneous T-cell Lymphoma-Sezary Syndrome; SD=stable disease; T-PLL=T-cell prolymphocytic leukaemia; Dx=diagnosis; Tx=therapy.

*

Received NMA HCT as part of the primary therapy due to poor-risk disease characteristics or histology.

ASCT was performed as part of planned tandem autologous-NMA allogeneic transplantation.