Previous studies provide a rationale for administration of AZA after allo SCT for decreasing chimerism. The investigators hypothesize that azacitidine can be well tolerated after SCT and help decrease rate of decreasing donor chimerism and hence decrease relapse without increasing GVHD
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
43
azacitidine 32mg/m2 x 5 days every 28 days for minimum of 4 cycles if tolerated
Henry ford hospital
Detroit, Michigan, United States
RECRUITINGThe rate of increase or stable donor chimerism
To determine the rate of increase or stable donor chimerism when using low dose azacitidine post allogenic stem cell transplant (SCT) in patients with acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML) and myeloproliferative neoplasms (MPN) with documented low or decreasing donor chimerism
Time frame: one year
NALINI JANAKIRAMAN, MD
CONTACT
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