Table 3.

Clinical characteristics of the 4 patients who developed clonal cytogenetic abnormalities without the morphologic features of myelodysplastic syndrome

Patient no.Age at diagnosis of AA, ySeverity of AA at diagnosisPrevious therapiesResponse to treatment after 6 moCumulative dose of G-CSF, mg/kgNo. of days of G-CSF therapyDuration of AA to MDS, moKaryotypeSurvival from diagnosis of AA, mo
Moderate None NR 1.1 68 37 + 8 > 82 
12 Very severe None PR 0.7 122 12 + 8 > 69 
18 Very severe None NR 2.1 214 19 del(13)(q14q21) > 73 
Moderate HDMP, CyA, AND NR 1.5 95 58 + 8 > 873-150 
Patient no.Age at diagnosis of AA, ySeverity of AA at diagnosisPrevious therapiesResponse to treatment after 6 moCumulative dose of G-CSF, mg/kgNo. of days of G-CSF therapyDuration of AA to MDS, moKaryotypeSurvival from diagnosis of AA, mo
Moderate None NR 1.1 68 37 + 8 > 82 
12 Very severe None PR 0.7 122 12 + 8 > 69 
18 Very severe None NR 2.1 214 19 del(13)(q14q21) > 73 
Moderate HDMP, CyA, AND NR 1.5 95 58 + 8 > 873-150 

AA indicates aplastic anemia; G-CSF, granulocyte colony-stimulating factor; MDS, myelodysplastic syndrome; NR, no response; and PR, partial response; HDMP, high-dose methylprednisolone; CyA, cyclosporin; AND, androgen.

F3-150

Patient underwent bone marrow transplantation.

or Create an Account

Close Modal
Close Modal