Renal function with cyclosporine C2 monitoring, enteric-coated mycophenolate sodium and basiliximab:: a 12-month randomized trial in renal transplant recipients

被引:11
作者
Cibrik, Diane
Meier-Kriesche, Herwig-Ulf
Bresnahan, Barbara
Wu, You Min
Klintmalm, Goran
Kew, Clifton E.
Kuo, Paul C.
Whelchel, John
Cohen, David
Baliga, Prabakar
Akalin, Enver
Benedetti, Enrico
Wright, Francis
Lieberman, Bonnie
Ulbricht, Bettina
Jensik, Stephen
机构
[1] Univ Michigan, Dept Internal Med, Div Nephrol, Ann Arbor, MI 48109 USA
[2] Univ Florida, Dept Med, Gainesville, FL USA
[3] Med Coll Wisconsin, Dept Nephrol, Milwaukee, WI 53226 USA
[4] Univ Arkansas, Sch Med, Transplant Serv, Little Rock, AR 72204 USA
[5] Baylor Univ, Med Ctr, Transplantat Serv, Dallas, TX 75246 USA
[6] Univ Alabama, Dept Nephrol, Birmingham, AL USA
[7] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[8] Piedmont Hosp, Transplantat Serv, Atlanta, GA USA
[9] Columbia Univ, Med Ctr, Dept Med, New York, NY USA
[10] Med Univ S Carolina, Charleston, SC 29425 USA
[11] Mt Sinai Med Ctr, Miller Transplant Inst, New York, NY 10029 USA
[12] Univ Illinois, Chicago, IL USA
[13] Methodist Specialty & Transplant Hosp, San Antonio, TX USA
[14] Novartis Pharmaceut Corp, Med Affairs, E Hanover, NJ USA
[15] Rush Presbyterian St Lukes Med Ctr, Organ & Tissue Transplant Serv, Chicago, IL 60612 USA
关键词
C-2; monitoring; cyclosporine microemulsion; enteric-coated mycophenolate sodium; high-risk recipient; kidney transplant; myfortic; renal function;
D O I
10.1111/j.1399-0012.2006.00622.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Cyclosporine exposure, as estimated by the area under the curve (AUC), predicts outcomes in renal transplantation. Cyclosporine concentration at two h post-dose (C-2) has been shown to be the most reliable, single-point surrogate marker for AUC. The objective of this study was to measure renal function beyond month 2 post-transplant using two different C-2 maintenance targets in combination with enteric-coated mycophenolate sodium (EC-MPS), corticosteroids, and basiliximab induction. Methods: In this open-label, multicenter trial, renal transplant recipients entered one of two randomized groups at day 61 post-transplant: group A (higher-C-2 range) or group B (lower-C-2 range). Results: Patients (164) were recruited, and 141 patients were entered the randomized groups (group A, n = 66; group B, n = 75). At 12 months, the mean calculated creatinine clearance was significantly greater in group B than in group A (79.2 vs. 71.0 mL/min, p < 0.05). Biopsy-proven acute rejection occurred in 14.7% patients in group B and in 24.2% patients in group A (n.s.). During the 12-month trial, 17.7% patients discontinued EC-MPS because of adverse events. Group B (44.0%) had fewer serious adverse events when compared with group A (62.1%; p = 0.04). Overall patient and graft survival were 99.4% and 95.7% respectively. Among 99 high-risk patients (i.e., African-American race, previous transplant, PRA > 35% or > 4 HLA mismatches), mean creatinine clearance at 12 months was 65.6 mL/min and biopsy-proven rejection occurred in 20.2% patients. Conclusions: Low cyclosporine C-2 levels are associated with improved renal function compared with higher C-2 levels when used in conjunction with EC-MPS, steroids and basiliximab induction. EC-MPS with low cyclosporine C-2 levels, corticosteroids and basiliximab provides excellent renal function with good efficacy even in high-risk patients.
引用
收藏
页码:192 / 201
页数:10
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