Table 1

Patient characteristics (n = 30)

No. of patients/No. of evaluable patientsMeanRange
Age, y    
 <10 13 14 0.5-45 
 10-20 11   
 21-40   
 >40   
Body weight, kg  39 5-83 
Karnofsky index, %  65 20-100 
Diagnosis    
 Acute lymphoblastic leukemia 14   
 Acute myeloid leukemia   
 Chronic myeloid leukemia   
 Myelodysplastic syndrome   
 Solid tumor   
 Immunodeficiency   
 Congenital bone marrow failure   
 Non-Hodgkin lymphoma   
Graft    
 Matched unrelated donor   
 Matched sibling donor   
 Mismatched unrelated donor (<9/10 matched)   
 Haploidentical HSCT from parents or siblings 17   
T-cell depletion    
 In vivo depletion (ATG)   
 Graft manipulation (plus serotherapy) 17   
 Alemtuzumab   
Antiviral drugs for treatment of AdV    
 Cidofovir    
 Before ACT 28/29   
 After ACT 20/27   
 Ribavirin 19/26   
Time of first positive AdV PCR in days after HSCT    
 In stool (n = 30)  29 –80-275 
 In blood (n = 28)  36 –71-305 
Days to ACT after HSCT (± SD)]  56 ± 61  
 <50 25   
 50-100   
 >100   
No. of patients/No. of evaluable patientsMeanRange
Age, y    
 <10 13 14 0.5-45 
 10-20 11   
 21-40   
 >40   
Body weight, kg  39 5-83 
Karnofsky index, %  65 20-100 
Diagnosis    
 Acute lymphoblastic leukemia 14   
 Acute myeloid leukemia   
 Chronic myeloid leukemia   
 Myelodysplastic syndrome   
 Solid tumor   
 Immunodeficiency   
 Congenital bone marrow failure   
 Non-Hodgkin lymphoma   
Graft    
 Matched unrelated donor   
 Matched sibling donor   
 Mismatched unrelated donor (<9/10 matched)   
 Haploidentical HSCT from parents or siblings 17   
T-cell depletion    
 In vivo depletion (ATG)   
 Graft manipulation (plus serotherapy) 17   
 Alemtuzumab   
Antiviral drugs for treatment of AdV    
 Cidofovir    
 Before ACT 28/29   
 After ACT 20/27   
 Ribavirin 19/26   
Time of first positive AdV PCR in days after HSCT    
 In stool (n = 30)  29 –80-275 
 In blood (n = 28)  36 –71-305 
Days to ACT after HSCT (± SD)]  56 ± 61  
 <50 25   
 50-100   
 >100   

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