Table 1

Patient characteristics

DiagnosisALLCML
No. of patients 15 
Imatinib therapy before HCT, no. 14 
Disease phase, no
    CR1, CR2 14, 1 — 
    AP, CP2, CP3, BC remission — 2, 2, 2, 1 
Median age, y (range) 37 (4-49) 44 (24-62) 
Sex, male/female 7/8 3/4 
Donor, no
    Related 
    Unrelated 
Stem cell source, no
    Peripheral blood 10 
    Marrow 
    Cord blood 
Conditioning, no
    TBI-based 15 
    Non-TBI-based 
GVHD prophylaxis, no
    Methotrexate/cyclosporine 
    Methotrexate/tacrolimus 
    Sirolimus/tacrolimus with or without methotrexate 
    Mycophenolate mofetil/tacrolimus 
    Methylprednisolone/cyclosporine/ATG 
Intrathecal methotrexate after HCT, no
    Yes 10 
    No 
Cytomegalovirus, no
    No reactivation 12 
    Ganciclovir/valganciclovir before day 90 4* 
DiagnosisALLCML
No. of patients 15 
Imatinib therapy before HCT, no. 14 
Disease phase, no
    CR1, CR2 14, 1 — 
    AP, CP2, CP3, BC remission — 2, 2, 2, 1 
Median age, y (range) 37 (4-49) 44 (24-62) 
Sex, male/female 7/8 3/4 
Donor, no
    Related 
    Unrelated 
Stem cell source, no
    Peripheral blood 10 
    Marrow 
    Cord blood 
Conditioning, no
    TBI-based 15 
    Non-TBI-based 
GVHD prophylaxis, no
    Methotrexate/cyclosporine 
    Methotrexate/tacrolimus 
    Sirolimus/tacrolimus with or without methotrexate 
    Mycophenolate mofetil/tacrolimus 
    Methylprednisolone/cyclosporine/ATG 
Intrathecal methotrexate after HCT, no
    Yes 10 
    No 
Cytomegalovirus, no
    No reactivation 12 
    Ganciclovir/valganciclovir before day 90 4* 

Numbers indicate numbers of patients unless otherwise indicated.

CR indicates complete remission; AP, accelerated phase; CP, chronic phase; BC, blast crisis; TBI, total body irradiation; ATG, antithymocyte globulin; —, not applicable.

*

One patient did not develop reactivation of CMV but was receiving either valganciclovir or placebo as part of a randomized CMV prophylaxis study.

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