Campath induction for kidney transplantation: report of 297 cases

To evaluate 297 adult renal transplantation patients who received Campath-1H-based induction protocol. Single center Institutional Review Board approved retrospective chart review of 297 patients who received alemtuzumab induction between November 2003 and December 2005. Maintenance immunosuppressio...

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Bibliographic Details
Published inTransplantation Vol. 85; no. 11; p. 1550
Main Authors Ortiz, Jorge, Palma-Vargas, Juan, Wright, Francis, Bingaman, Adam, Agha, Irfan, Rosenblatt, Steven, Foster, Preston
Format Journal Article
LanguageEnglish
Published United States 15.06.2008
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Summary:To evaluate 297 adult renal transplantation patients who received Campath-1H-based induction protocol. Single center Institutional Review Board approved retrospective chart review of 297 patients who received alemtuzumab induction between November 2003 and December 2005. Maintenance immunosuppression consisted of tacrolimus, mycophenolate mofetil, and rapidly tapered solumedrol with few exceptional cases. The mean patient follow-up was 362 days. All rejection episodes were biopsy confirmed. Posttransplant infection rates were recorded. There were 153 living donor and 144 deceased donor recipients. One-year survival rates for recipient and kidney allografts were 100% and 98% for living donors, 97.4% and 89.7% for non-extended criteria donors (ECD) deceased donors, and 85.7% and 89.3% for ECD deceased donors. The overall rejection rate was 7%. Overall infectious rate was 19.8%. We had no cases of posttransplant lymphoproliferative disease. Of the 289 recipients discharged off prednisone, 269 (93%) remain steroid free. Alemtuzumab and reduced dosages of tacrolimus and mycophenolate without long-term steroids can achieve low rates of rejection and excellent graft and patient survival without excessive risk of infection or malignancy. There is still a need for large randomized trials with long-term follow-up to determine its exact role in solid organ transplantation.
ISSN:0041-1337
DOI:10.1097/TP.0b013e31816f60cf