Skip to main content
. 2018 Aug 6;82(4):717–721. doi: 10.1007/s00280-018-3659-8

Table 1.

Patient characteristics as N (%) or median (range)

PHT LEV
N 70 34
Male sex 46 (65.7) 18 (52.9)
Age (years) 58 (17–74) 58 (35–69)
Diagnosis
 AML 40 (57.1) 10 (29.4)
 MDS 24 (34.3) 11 (32.4)
 CML 4 (5.7) 3 (8.8)
 PCNSL 0 5 (14.7)
 DLBCL 2 (2.9) 0
 Other 0 5 (14.7)
Donor/stem cell source
 Autologous peripheral blood 0 5 (14.7)
 Related peripheral blood 14 (20.0) 4 (11.8)
 Unrelated peripheral blood 0 5 (14.7)
 Unrelated bone marrow 42 (60.0) 10 (29.4)
 Unrelated cord blood 14 (20.0) 10 (29.4)
Conditioning regimen
 ivBu/CY 20 (28.6) 9 (26.5)
 FB4 8 (11.4) 0
 ATG/FB4 ± AraC 37 (52.9) 18 (52.9)
 FB4/TBI ± AraC 2 (2.9) 4 (11.8)
 ivBu2 + α 3 (4.3) 0
 ivBu4 + β 0 3 (8.8)
Emesis prophylaxis
 Granisetron 70 (100) 10 (29.4)
 Palonosetron 0 1 (2.9)
 Palonosetron + fosaprepitant 0 23 (67.6)

AML acute myeloid leukemia, MDS myelodysplastic syndrome, CML chronic myeloid leukemia, PCNSL primary central nervous system lymphoma, DLBCL diffuse large B cell lymphoma, ivBu/CY intravenous busulfan at 12.8 mg/kg + cyclophosphamide, ivBu2 + α intravenous busulfan at 6.4 mg/kg + other drugs, FB4 fludarabine + intravenous busulfan at 12.8 mg/kg, ATG anti-thymocyte globulin (rabbit), AraC cytarabine, TBI total body irradiation, ivBu4 + β intravenous busulfan at 12.8 mg/kg + other drugs, PHT phenytoin, LEV levetiracetam.