320 Risk of CMV after r-ATG or IL2 Antagonist Induction and the Impact of CMV-Directed Prophylaxis in Low Risk Renal Transplant Recipients

Tuesday, October 23, 2012: 10:15 AM
Westin Diplomat Resort
Teena Sam, PharmD, BCPS1, Elise Carlson, PharmD2, Ian C. Doyle, PharmD, BCPS3, Steven Gabardi, PharmD, BCPS4, Karen L. Hardinger, PharmD, BCPS5, John Knorr, PharmD, BCPS6, Lisa M. McDevitt, Pharm.D., BCPS7, Kimi Ueda, PharmD, BCPS8 and Eric Tichy, Pharm.D., BCPS1
1Yale-New Haven Hospital, New Haven, CT
2Sanford Health, Fargo, ND
3Pacific University Oregon School of Pharmacy, Hillsboro, OR
4Department of Pharmacy & Renal Divison, Brigham & Women's Hospital; Department of Medicine, Harvard Medical School, Boston, MA
5UMKC School of Pharmacy, Kansas City, MO
6Albert Einstein Medical Center, Philadelphia, PA
7Tufts Medical Center, Boston, MA
8California Pacific Medical Center, San Francisco, CA

Purpose: Rabbit antithymocyte globulin (r-ATG) induction is associated with an increased risk for CMV after transplant.  Limited data exists for optimal antiviral prophylaxis strategies in low CMV risk (D-/R-) renal transplant recipients (RTRs) receiving r-ATG. Our objective was to compare risk of CMV disease associated with r-ATG versus IL2 antagonist (IL2) induction and the impact of CMV-directed prophylaxis on the incidence of CMV disease in D-/R- RTRs who received r-ATG induction.

Methods: A multicenter, retrospective analysis evaluated adult D-/R- RTRs between 01/01/04 to 09/30/A multicenter, retrospective analysis evaluated adult D-/R- RTRs between 01/01/04 to 09/30/2010.  All patients received induction therapy with either r-ATG or IL2 plus maintenance immunosuppression with tacrolimus, mycophenolic acid, with or without steroids. Group A (n=118) received r-ATG induction without CMV-directed antiviral prophylaxis. Group B (n=41) received r-ATG induction with CMV-directed prophylaxis using valganciclovir. Group C (n=73) received IL2 induction without CMV-directed antiviral prophylaxis. The primary endpoint was CMV disease incidence and secondary endpoints included CMV viremia, acute rejection (AR), antibody mediated rejection (AMR), and other opportunistic infections (OIs) at 1 year post-transplant.

Results: Differences in baseline characteristics included proportion of living donor transplants (24.4%, 60.2% vs 75.3%), rate of early steroid withdrawal (2.4%, 48.8% vs 19.2%), and mean duration of antiviral prophylaxis (5.1, 3.0 vs 3.5 months) in group A, B and C, respectively (p<0.05). There was no difference in rate of CMV disease (0.0%, 0.8% vs 1.4%) or rate of AR (14.6%, 14.4%, vs 19.2%) in groups A, B and C, respectively (p>0.05). Similarly, there were no significant differences in rate of AMR, BK or HSV infection.

Conclusion: Our study demonstrates that the incidence of CMV disease in D-/R- RTRs is rare, regardless of induction or antiviral prophylaxis strategy utilized.  Non-CMV-directed prophylaxis may provide sufficient efficacy and potentially offer significant cost avoidance in this population.