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Related Experiment Videos

From cyclosporine to the future.

C Ponticelli1, A Tarantino, M Campise

  • 1Division of Nephrology, Ospedale Maggiore IRCCS, Milano, Italy. Ponticelli@policlinico.mi.it

Transplantation Proceedings
|March 26, 2004
PubMed
Summary

Cyclosporine (CsA) demonstrates improved long-term graft survival in kidney transplant patients compared to azathioprine. Monotherapy with CsA reduces side effects, while basiliximab addition lowers acute rejection rates.

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Area of Science:

  • Nephrology
  • Immunosuppression
  • Transplantation

Background:

  • Cyclosporine (CsA) is a cornerstone of immunosuppression in renal transplantation.
  • Extensive clinical trials have evaluated various CsA-based regimens.
  • Long-term outcomes and side effect profiles remain critical considerations.

Purpose of the Study:

  • To review cumulative experience with CsA in renal transplantation.
  • To assess the efficacy and safety of different CsA-based immunosuppressive strategies.
  • To identify current challenges and future directions in immunosuppression.

Main Methods:

  • Analysis of data from multiple randomized controlled trials and multicenter studies.
  • Review of cumulative patient experience and graft survival data.

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  • Inclusion of ongoing trials investigating novel immunosuppressive agents.
  • Main Results:

    • CsA-treated patients showed better 10-year graft survival than azathioprine.
    • CsA monotherapy and double/triple therapy demonstrated similar long-term graft survival, with monotherapy having fewer steroid side effects.
    • Addition of basiliximab to triple therapy reduced acute rejection without increasing side effects.
    • Mean graft half-life was 18.7 years for cadaver and 31.9 years for living donors.
    • No significant graft function decline observed in grafts functioning at 15 years.

    Conclusions:

    • CsA-based immunosuppression offers favorable long-term graft survival in renal transplantation.
    • Minimizing steroid use through monotherapy or alternative agents is beneficial.
    • Ongoing research focuses on addressing calcineurin inhibitor nephrotoxicity and steroid-related cardiovascular risks with newer agents.