Table 1

Patient characteristics of patients who started with lenalidomide

Patient characteristicValue
Total no. 30 
Male/female 19/10 
Median age, y (range) 53 (37-65) 
WHO performance status 0/1/2 20/9/1 
ISS stage at diagnosis I/II/III 9/11/10 
Induction therapy before HDM  
VAD/TAD/PAD 17/4/9 
Conditioning NMA allo-SCT  
TBI/TBI + fluda/TBI + fluda + ATG 28/1/1 
Median CD34+-infused stem cells, × 106/kg (range) 5.9 (2.0-10.9) 
Median time between allo-SCT and start of lenalidomide, wk (range) 12 (4-27) 
Patient characteristicValue
Total no. 30 
Male/female 19/10 
Median age, y (range) 53 (37-65) 
WHO performance status 0/1/2 20/9/1 
ISS stage at diagnosis I/II/III 9/11/10 
Induction therapy before HDM  
VAD/TAD/PAD 17/4/9 
Conditioning NMA allo-SCT  
TBI/TBI + fluda/TBI + fluda + ATG 28/1/1 
Median CD34+-infused stem cells, × 106/kg (range) 5.9 (2.0-10.9) 
Median time between allo-SCT and start of lenalidomide, wk (range) 12 (4-27) 

WHO indicates World Health Organization; ISS, International Staging System; HDM, high-dose melphalan; VAD, vincristine, adriamycin, and dexamethasone; TAD, thalidomide, adriamycin, and dexamethasone; PAD, bortezomib, adriamycin, and dexamethasone; TBI total body irradiation; and fluda, fludarabine.

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