Abstract 4209

Background:

Recurrence of disease remains a significant cause of morbidity and mortality in patients who undergo allogeneic SCT for AML and MDS. Low-dose azacitidine is currently under investigation in the post-transplant setting with the goal of prolonging disease-free survival and decreasing relapse rates. It is unclear if there is potential pharmacologic interaction between azacitidine and dose-adjusted tacrolimus used to prevent post-transplant graft-versus-host disease (GVHD), a clinically relevant question since any resultant tacrolimus under- or over-dosing may lead to increased risk of GVHD or drug toxicity, respectively. We hypothesized that azacitidine does not significantly interact with tacrolimus levels and performed a retrospective analysis to test this hypothesis.

Patients and Methods:

We reviewed tacrolimus daily doses and serum drug levels of 62 AML and MDS patients who received azacitidine maintenance therapy (n=30) or no maintenance therapy (n=32) following allogeneic stem cell transplantation at MD Anderson Cancer Center between 2008–2012. Patient characteristics are summarized in the Table. Patients in the maintenance cohort received subcutaneous azacitidine at 32 mg/m2 on days 1–5 repeated every 28 days starting at a median time of post-transplant day +65 (range 43–100). Tacrolimus doses and serum levels were averaged for 28 days for each patient before and after initiation of azacitidine maintenance and at day +66 in the non-maintenance cohort. Differences between the two cohorts in their mean change of tacrolimus doses and serum drug levels were assessed using a Student's t-test.

Results:

Mean (SD) oral tacrolimus doses pre- and post-maintenance therapy were 2.61 (2.13) mg daily and 2.44 (2.15) mg daily in the azacitidine group and 2.54 (1.86) mg and 2.23 (1.39) mg daily in the non-azacitidine cohort. This resulted in a mean change in tacrolimus dosing of -0.17 (1.16) mg daily in the azacitidine patients and -0.31 (1.10) mg daily in the non-maintenance group (p=0.62). Mean (SD) serum tacrolimus levels pre- and post-maintenance therapy were 8.07 (1.16) ng/mL and 7.58 (2.32) ng/mL in the azacitidine group and 8.23 (1.49) ng/mL and 7.10 (1.69) ng/mL in patients on no maintenance therapy. This resulted in a mean change in serum tacrolimus levels of -0.49 (2.75) ng/mL in the azacitidine cohort and -1.13 (2.04) ng/mL in the non-maintenance group (p=0.30).

Conclusion:

Maintenance azacitidine therapy following allo-SCT for AML and MDS does not appear to affect concurrent tacrolimus dosing or serum drug levels.

Table.

Patient Characteristics

AZA (N=30)No AZA (N=32)p-value
Gender, n (%)    
    Male 17 (56.7) 22 (68.8) 0.43a 
    Female 13 (43.3) 10 (31.3)  
Age at transplant (years)    
    Mean (SD) 51.2 (14.5) 52.5 (14.3) 0.74b 
    Median (range) 54 (19–72) 57 (20–70)  
Diagnosis, n (%)    
    AML 26 (86.7) 26 (81.3) 0.73a 
    MDS 4 (13.3) 6 (18.8)  
Donor type, n (%)    
    Match unrelated donor 10 (33.3) 15 (46.9) 0.69a 
    Match related 16 (53.3) 12 (37.5)  
    Mismatch unrelated 3 (10.0) 4 (12.5)  
    Haploidentical 1 (3.3) 1 (3.1)  
Stem cell source, n (%)    
    Peripheral blood 19 (63.3) 22 (68.8) 0.68a 
    Bone Marrow 10 (33.3) 8 (25.0)  
    Cord 1 (3.3) 2 (6.3)  
Conditioning regimen, n (%)    
    Fludarabine/Busulfan 15 (50.0) 15 (46.9) 1.00a 
    Fludarabine/Melphalan 11 (36.7) 12 (37.5)  
    Other 4 (13.3) 5 (15.6)  
GVHD prophylaxis, n (%)    
    Tacrolimus/Methotrexate 27 (90.0) 27 (84.4) 0.71a 
    Tacrolimus/Cyclophosphamide/MMF 1 (3.3) 3 (9.4)  
    Tacrolimus/MMF 1 (3.3) 2 (6.3)  
    Tacrolimus/Cyclophosphamide 1 (3.3) 0 (0.0)  
AZA (N=30)No AZA (N=32)p-value
Gender, n (%)    
    Male 17 (56.7) 22 (68.8) 0.43a 
    Female 13 (43.3) 10 (31.3)  
Age at transplant (years)    
    Mean (SD) 51.2 (14.5) 52.5 (14.3) 0.74b 
    Median (range) 54 (19–72) 57 (20–70)  
Diagnosis, n (%)    
    AML 26 (86.7) 26 (81.3) 0.73a 
    MDS 4 (13.3) 6 (18.8)  
Donor type, n (%)    
    Match unrelated donor 10 (33.3) 15 (46.9) 0.69a 
    Match related 16 (53.3) 12 (37.5)  
    Mismatch unrelated 3 (10.0) 4 (12.5)  
    Haploidentical 1 (3.3) 1 (3.1)  
Stem cell source, n (%)    
    Peripheral blood 19 (63.3) 22 (68.8) 0.68a 
    Bone Marrow 10 (33.3) 8 (25.0)  
    Cord 1 (3.3) 2 (6.3)  
Conditioning regimen, n (%)    
    Fludarabine/Busulfan 15 (50.0) 15 (46.9) 1.00a 
    Fludarabine/Melphalan 11 (36.7) 12 (37.5)  
    Other 4 (13.3) 5 (15.6)  
GVHD prophylaxis, n (%)    
    Tacrolimus/Methotrexate 27 (90.0) 27 (84.4) 0.71a 
    Tacrolimus/Cyclophosphamide/MMF 1 (3.3) 3 (9.4)  
    Tacrolimus/MMF 1 (3.3) 2 (6.3)  
    Tacrolimus/Cyclophosphamide 1 (3.3) 0 (0.0)  
a

Fisher's exact test,

b

Student's t-test

Disclosures:

Off Label Use: azacitidine: off-label use as maintenance therapy following allogeneic stem cell transplant for MDS/AML. Champlin:Otsuka: Research Funding. De Lima:Celgene: Research Funding.

Author notes

*

Asterisk with author names denotes non-ASH members.

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