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Transplantation ; 96(12): 1073-81, 2013 Dec 27.
Article in English | MEDLINE | ID: mdl-24345868

ABSTRACT

BACKGROUND: Everolimus (EVR) has demonstrated good efficacy after renal transplantation. Racial disparities in clinical outcomes after de novo renal transplantation are well documented; whether the efficacy of EVR varies based on recipient ethnicity is unknown. We conducted a comparative risk assessment of EVR by ethnicity. METHODS: Data on 2004 renal transplant recipients from three EVR studies were pooled to identify the impact of ethnicity on efficacy outcomes across EVR dosing groups and control groups. Ethnic groups compared were African Americans, non-U.S. blacks, Asians, Hispanics, and Caucasians. EVR groups received either 1.5 or 3 mg per day, with either standard-dose cyclosporine or reduced-dose cyclosporine. Control groups received mycophenolic acid (MPA) with standard-dose cyclosporine. Composite efficacy failure endpoint was graft loss, death, biopsy-proven acute rejection, or lost to follow-up. Adjusted odds ratios were calculated using a logistic regression model. RESULTS: The proportion of renal transplant recipients who met the composite endpoint was African Americans (46%), non-U.S. black (35%), Caucasian (31%), Hispanic (28%), and Asian (25%). The odds of meeting the composite endpoint were significantly (P=0.0001) greater for African Americans versus Caucasians but did not differ among the other ethnic groups (ethnic groups were only compared with Caucasians). EVR and MPA were associated with similar efficacy among each of the ethnic groups. CONCLUSION: In this pooled data analysis in more than 2000 renal transplant recipients, EVR versus MPA resulted in similar composite endpoint incidence events across ethnicities. Consistent with previously published data, African Americans had poorer clinical outcomes. EVR is efficacious regardless of ethnicity.


Subject(s)
Kidney Transplantation/methods , Mycophenolic Acid/therapeutic use , Renal Insufficiency/therapy , Risk Assessment , Sirolimus/analogs & derivatives , Adult , Black or African American , Creatinine/metabolism , Cyclosporine/administration & dosage , Everolimus , Female , Humans , Immunosuppressive Agents/therapeutic use , Logistic Models , Male , Middle Aged , Multicenter Studies as Topic , Odds Ratio , Randomized Controlled Trials as Topic , Renal Insufficiency/ethnology , Sirolimus/therapeutic use , Treatment Outcome
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