Outcomes at 3 years of a prospective pilot study of Campath-1H and sirolimus immunosuppression for renal transplantation

被引:61
作者
Barth, Rolf N.
Janus, Christina A.
Lillesand, Christine A.
Radke, Nancy A.
Pirsch, John D.
Becker, Bryan N.
Fernandez, Luis A.
Chin, L. Thomas
Becker, Yolanda T.
Odorico, Jon S.
D'Alessandro, Anthony M.
Sollinger, Hans W.
Knechtle, Stuart J.
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Dept Surg, Div Transplantat, Madison, WI 53792 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Nephrol Sect, Madison, WI 53792 USA
关键词
immunosuppression; kidney; transplant; sirolimus Campath-1H;
D O I
10.1111/j.1432-2277.2006.00388.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Campath-1H (alemtuzumab) induction was used for renal transplantation in combination with sirolimus as immunosuppression. We previously reported a high (28%) rate of early rejection with this regimen, and now report 3-year outcomes. Twenty-nine patients were recipients of either deceased donor or non-HLA (Human Leukocyte Antigen) identical living donor primary renal allografts. Clinical parameters including infection, malignancy, kidney function, and kidney histology were followed prospectively for 3 years. Three-year cumulative graft and patient survival were 96% and 100%, respectively. Twenty patients were maintained on steroid-free immunosuppressive regimens, and 15 patients were maintained on monotherapy for immunosuppression (12 on sirolimus). No serious infectious complications were observed and two patients developed basal cell skin cancer. The 3-year results of our initial pilot study demonstrate good graft (96%) and patient (100%) outcomes. Campath-1H induction has yielded a high proportion of patients maintained on immunosuppressive monotherapy (57%) without serious infectious- and no malignancy-related complications. The reported regimen yielded novel insights into both Campath-1H and sirolimus therapy in renal transplantation. Because of the higher incidence of early rejection, we recommend a modified strategy of immunosuppression including a brief course of a calcineurin inhibitor.
引用
收藏
页码:885 / 892
页数:8
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