Skip to search boxSkip to navigationSkip to main content

Randomized double-blind study of immunoprophylaxis with basiliximab, a chimeric anti-interleukin-2 receptor monoclonal antibody, in combination with mycophenolate mofetil-containing triple therapy in renal transplantation

  • Joseph G. Lawen(corresponding author)
    ,
  • Elizabeth A. Davies
    ,
  • Georges Mourad
    ,
  • Frederic Oppenheimer
    ,
  • Miguel Gonzalez Molina
    ,
  • Lionel Rostaing
*Corresponding author for this work
  • QEII Health Sciences Centre
    ,
  • Ohio State University
    ,
  • CHU Montpellier
    ,
  • Hospital Clinico Villaroel
    ,
  • Hospital Regional Universitario Carlos Haya
    ,
  • CHU de Toulouse
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Background. Acute rejection remains a major problem in renal transplantation. Immunoprophylaxis with basiliximab (Simulect) has achieved significant reductions in acute rejection episodes in renal allograft recipients receiving dual immunosuppression. This study explored the tolerability and cumulative benefit of combining basiliximab with triple-drug therapy-cyclosporine (USP Modified, Neoral), mycophenolate mofetil, and steroids. Methods. In a randomized, double-blind, placebocontrolled, multicenter study, 123 kidney transplant recipients received either basiliximab at 20 mg before transplantation (day 0) and 20 mg on day 4 (n=59), or placebo (n=64). All received triple-drug immunosuppression and were followed for 6 months. Results. Tolerability of basiliximab was equivalent to placebo, with no increase in serious adverse events, infection, malignancy, or posttransplant lymphoproliferative disorder. At 6 months, there were trends in favor of basiliximab over placebo in the incidences of first biopsy-confirmed acute rejection (15.3% vs. 26.6%, P=NS) and of acute rejection treated with antibody (5.1% vs. 15.6%, P=NS). Kaplan-Meier estimates at 4 weeks and 6 months were significantly in favor of basiliximab treatment for first acute rejection, biopsyconfirmed rejection, rejection episodes treated with antibody therapy, and treatment failure. Renal function improved more rapidly in the basiliximab group, with mean creatinine clearance at week 2 being 54.7 mL/min versus 43.2 mL/min for placebo (P=0.034). At 12 months, patient survival was 100% in both groups; graft survival was 94.9% with basiliximab and 92.2% with placebo. Conclusions. Basiliximab immunoprophylaxis is safe, well tolerated, and shows a trend toward reduction in number of acute rejection episodes in renal transplant patients receiving cyclosporine, mycophenolate mofetil, and steroids.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 37-43 (7 pages)

Journal (Volume, Issue Number)

Transplantation (Volume 75, Issue 1)

Publication milestones

  • Published - 01/15/2003

Publication status

Published - 01/15/2003

ISSN

0041-1337

Publication IDs

  • Scopus: 0037439677
  • PubMed: 12544868

Publication metrics

Metrics

SciVal
citations
116
Scopus
citations
SciVal
FWCI
5.23
SciVal
Author count
12
SciVal
Paper percentile
95
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.08
Fractional count
11
Fractional count
0.92
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
36
Citation count
129