451 Sub-Therapeutic Levels of ORAL Tacrolimus Prophylaxis PRIOR to Allogeneic STEM CELL Transplant Do NOT Predict the Incidence of Chronic GRAFT Versus HOST Disease

Track: Contributed Abstracts
Saturday, February 16, 2013, 6:45 PM-7:45 PM
Hall 1 (Salt Palace Convention Center)
Jill MacPherson, DNP, RN, FNP-BC, AOCNP , Adult Blood and Marrow Transplant, Texas Transplant Institute, San Antonio, TX
Carlos Bachier, MD , Adult Blood and Marrow Transplant, Texas Transplant Institute, San Antonio, TX
Ashley Simpson, PA-C , Adult Blood and Marrow Transplant, Texas Transplant Institute, San Antonio, TX
Paul J. Shaughnessy, MD , Adult Blood and Marrow Transplant, Texas Transplant Institute, San Antonio, TX
SUB-THERAPEUTIC LEVELS OF ORAL TACROLIMUS PROPHYLAXIS PRIOR TO ALLOGENEIC STEM CELL TRANSPLANT DO NOT PREDICT THE INCIDENCE OF CHRONIC GRAFT VERSUS HOST DISEASE

Jill MacPherson, Ashley Simpson, Carlos Bachier, Paul Shaughnessy

Chronic graft versus host disease (cGVHD) is a common complication of allogeneic stem cell transplantation (ASCT). Tacrolimus prophylaxis has been proven to be instrumental in the prevention of acute graft versus host disease (aGVHD) a common precursor to developing cGVHD. Our institution uses oral tacrolimus prior to ASCT because we perform ASCT in the outpatient setting and increases ease of administration. We retrospectively reviewed our experience in 94 consecutive patients (pts) who received ASCT from 10 /10 HLA matched donors, 47 were matched sibling donors (MSD) and 47matched unrelated donors (MUD) with a median age of 50 and 52 respectively. All patients received GVHD prophylaxis with tacrolimus started orally between day -3 and day -1 at a dose of 0.06mg/kg per day divided twice daily. Standard short course methotrexate (MTX) was prescribed for all pts (D1 dose 15mg/m2, D3, 6, and 11 doses at 10mg/m2). Pts who had sub-therapeutic tacrolimus levels (less than 5ug/L) on the day of transplant (D0) were compared to pts who had therapeutic tacrolimus levels (greater than 5ug/L) for incidence of cGVHD and overall survival. Sixty-eight pts had tacrolimus levels less than 5ug/L on D0 and 26 pts had tacrolimus of 5ug/L or greater. Fifty eight of the 94 patients developed cGVHD and 36 did not develop cGVHD indicating that there was no significant difference in the incidence of cGVHD in these patients despite the level of tacrolimus on D0. The 58 pts that developed cGVHD, 42/68 (62%) had a tacrolimus level less than 5ug/L.The 36 pts that did not develop cGVHD, 26/68 (38%) had a tacrolimus level less than 5ug/L. With a median follow up of 463 days 54/94 pts (57%) survive; 40/68 pts (59%) with D0 tacrolimus levels that were less than 5ug/L, and 14/26 pts (54%) with D0 tacrolimus levels were greater than or equal to 5ug/L. In conclusion, oral tacrolimus prophylaxis prior to ASCT at our institution results in sub-therapeutic levels on the day of transplant in the majority of patients, however, this does not appear to impact the overall incidence of cGVHD or survival. As an incidental finding, those who developed cGVHD had longer overall survival versus those who did not develop cGVHD. This study was limited by its retrospective nature, small size and single center experience.