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. Author manuscript; available in PMC: 2014 May 22.
Published in final edited form as: Br J Haematol. 2012 Mar 26;157(5):553–563. doi: 10.1111/j.1365-2141.2012.09099.x

Table 1.

Patient characteristics

N = 30 No. Percent
Age at transplant, median, year (range) 54.5 (36-70) -
Male 15 50
Multiple myeloma subtype
  IgG 15 50
  IgA 9 30
  Light chain 5 17
  Plasma cell leukemia 1 3
Chromosomal abnormality*1
  High risk 13 45
   13q deletion 11 38
   17p deletion 2 7
   t(4;14) 2 7
  Standard risk 16 55
β2 microglobulin, median, mg/L (range) 4.35 (1.8-11.4) -
Refractory disease*2 16 55
Albumin, median, g/dL (range) 3.7 (3.1-4.9) -
Time from diagnosis to enrollment, median, month
(range)
7 (3 – 80)*3 -
Prior chemotherapy
  Thalidomide/dexamethasone 14 46
  Lenalidomide-based regimen*4 11 37
  Vincristine/Adriamycin/dexamethasone (VAD) 5 17
  Liposomal doxorubicin-based regimen 3 10
Number of prior regimens
  1 23 77
  ≥2 7 23
Durie-Salmon Staging System*5
  1 3 10
  2 6 21
  3 20 69
International Staging System (ISS)
  I 8 27
  II 16 53
  III 6 20
*1

One patient with plasma cell leukemia was not included in the chromosomal risk classification.

*2

Disease progression during induction therapy or within 60 days of discontinuing induction therapy (prior to enrollment)

*3

One patient was diagnosed as asymptomatic myeloma 6 years prior to study enrollment and only required systemic therapy 4 months before the enrollment.

*4

Three patients received liposomal doxorubicin containing regimen.

*5

One patient with plasma cell leukemia was excluded.