Literature DB >> 11562416

Long-term results of a randomized study comparing three immunosuppressive schedules with cyclosporine in cadaveric kidney transplantation.

Giuseppe Montagnino1, Antonio Tarantino1, Giuseppe P Segoloni2, Vincenzo Cambi3, Gaetano Rizzo4, Paolo Altieri5, Marco Castagneto6, Maurizio Salvadori7, Maria Cossu8, Francesco Pisani9, Mario Carmellini10, Francesco Mastrangelo11, Roberto Ferrara12, Claudio Ponticelli1.   

Abstract

In this randomized controlled trial started in October 1990, 354 cadaveric kidney transplant recipients were assigned to receive either cyclosporine (CsA) monotherapy (115 patients), CsA + steroids (117 patients), or CsA + steroids + azathioprine (122 patients). The median follow-up was 85.1 mo. Thirty-one deaths occurred (infection, 12; cardiovascular disease, 11; neoplasia, 4; and others, 4), and 65 grafts were lost, mostly due to acute (15) or chronic rejection (50). The cumulative graft half-life was 18.1 yr. According to the "intention-to-treat," the 9-yr actuarial patient and graft survival were 94.0% and 73.3%, respectively, in monotherapy, 87.3% and 65.9% in dual therapy, and 87% and 72.2% in triple therapy (P = 0.647). At the last follow-up, the percentage of patients who remained with the original treatment was 51.2% in monotherapy, 81.7% in dual therapy, and 63.3% in triple therapy. At the seventh year, the mean creatinine clearances were 54.9 +/- 17.6 ml/min in monotherapy, 57.9 +/- 23.4 in dual therapy, and 60.6 +/- 20.7 in triple therapy (P = 0.375). Cataracts (P = 0.000), osteoporosis (P = 0.000), and cardiovascular complications (P = 0.000) were more frequent in dual or triple therapy than in monotherapy. Actuarial graft survival at 9 yr in patients on monotherapy who had to have steroids added was similar to that of the other two groups (62.2% versus 69.3%, P = 0.134). In conclusion, actuarial patient and graft survivals did not differ among the three schemes. The long-term renal function and survival were not affected in the patients on monotherapy who needed the addition of steroids. Monotherapy was associated with a lower incidence of extrarenal complications than the other two regimens.

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Year:  2001        PMID: 11562416     DOI: 10.1681/ASN.V12102163

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  7 in total

1.  Steroid withdrawal in renal transplant patients: the Irish experience.

Authors:  P J Phelan; A-M Moran; P O'Kelly; P Y Heng; S M Yussof; J J Walshe; C Magee; P J Conlon
Journal:  Ir J Med Sci       Date:  2010-10-29       Impact factor: 1.568

Review 2.  Systematic review of randomized controlled trial quality in pediatric kidney transplantation.

Authors:  Robert J Brooks; Gail Y Higgins; Angela C Webster
Journal:  Pediatr Nephrol       Date:  2010-08-06       Impact factor: 3.714

Review 3.  Calcineurin inhibitors in renal transplantation: what is the best option?

Authors:  Kazunari Tanabe
Journal:  Drugs       Date:  2003       Impact factor: 9.546

Review 4.  Immunosuppression for long-term maintenance of renal allograft function.

Authors:  Gerd Offermann
Journal:  Drugs       Date:  2004       Impact factor: 9.546

Review 5.  Interventions for preventing bone disease in kidney transplant recipients.

Authors:  Suetonia C Palmer; Edmund Ym Chung; David O McGregor; Friederike Bachmann; Giovanni Fm Strippoli
Journal:  Cochrane Database Syst Rev       Date:  2019-10-22

6.  Steroid- and calcineurin inhibitor free immunosuppression in kidney transplantation: state of the art and future developments.

Authors:  Markus Giessing; Tom Florian Fuller; Max Tuellmann; Torsten Slowinski; Klemens Budde; Lutz Liefeldt
Journal:  World J Urol       Date:  2007-02-28       Impact factor: 3.661

7.  Novel surgical techniques, regenerative medicine, tissue engineering and innovative immunosuppression in kidney transplantation.

Authors:  Maciej Nowacki; Łukasz Nazarewski; Tomasz Kloskowski; Dominik Tyloch; Marta Pokrywczyńska; Katarzyna Pietkun; Arkadiusz Jundziłł; Janusz Tyloch; Samy L Habib; Tomasz Drewa
Journal:  Arch Med Sci       Date:  2016-08-25       Impact factor: 3.318

  7 in total

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