Table 2.

Reversal of p15 hypermethylation and hematologic response of high-risk MDS patients after decitabine treatment

PatientHypermC reversalHematologic responseDAC coursesSurvival (mo)
001 Yes Blast reduction, hematologic improvement 27 
002 NM Progression to AML 
003 Yes Complete remission 16 
004 ND Progressive cytopenia 50 
005 Yes Blast reduction 15 
006 Yes Hematologic improvement 15 
007 Yes Complete remission 13 
008 No Progression to AML 11  
009 NM Blast reduction, hematologic improvement 31 
010 No Progressive cytopenia 10 
011 NM Hematologic improvement 38 
012 No Progression to AML 
013 Yes Complete remission 21  
014 ND Toxic death 2  
015 NM Partial remission 18 
016 Yes Blast reduction, tril hematologic improvement 44  
017 NM Stable disease 52 
018 Yes Blast reduction 5  
019 Yes Blast reduction, hematologic improvement 73  
020 NM Blast reduction, hematologic improvement 75 
021 NM Progression to AML 5  
022 ND No decitabine treatment — 
023 ND No decitabine treatment — 32+ 
PatientHypermC reversalHematologic responseDAC coursesSurvival (mo)
001 Yes Blast reduction, hematologic improvement 27 
002 NM Progression to AML 
003 Yes Complete remission 16 
004 ND Progressive cytopenia 50 
005 Yes Blast reduction 15 
006 Yes Hematologic improvement 15 
007 Yes Complete remission 13 
008 No Progression to AML 11  
009 NM Blast reduction, hematologic improvement 31 
010 No Progressive cytopenia 10 
011 NM Hematologic improvement 38 
012 No Progression to AML 
013 Yes Complete remission 21  
014 ND Toxic death 2  
015 NM Partial remission 18 
016 Yes Blast reduction, tril hematologic improvement 44  
017 NM Stable disease 52 
018 Yes Blast reduction 5  
019 Yes Blast reduction, hematologic improvement 73  
020 NM Blast reduction, hematologic improvement 75 
021 NM Progression to AML 5  
022 ND No decitabine treatment — 
023 ND No decitabine treatment — 32+ 

Reversal of p15 hypermethylation was defined as at least 25% reduction of methylation (relative to hypermethylation of more than 15% prior to treatment as given in Table 1). Thus, for the 7 patients with initial methylation of no more than 15%, reversal of hypermethylation was not measurable (NM). The total number of courses administered is given. Hematologic responses were defined as described in “Patients, materials, and methods.”12 Survival (in months) was from start of decitabine treatment (patients 001-021) or from diagnosis (patients 022, 023). For patient 001 at relapse and patient 018 during progression, p15 methylation was determined from peripheral blood MNCs because bone marrow MNCs were not available. ND indicates not done; —, no decitabine treatment; hematologic response not given because of early progression to AML (patient 022) and allogeneic transplantation as first line therapy (patient 023). Follow-up was until August 1, 2001.

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