Volume 8, Issue 2 pp. 171-177

Short sirolimus half-life in pediatric renal transplant recipients on a calcineurin inhibitor-free protocol

A. D. Schachter

A. D. Schachter

Division of Nephrology, Children's Hospital and Harvard Medical School, Boston, MA, USA

Children's Hospital Informatics Program, Children's Hospital, Boston, MA, USA

Search for more papers by this author
K. E. Meyers

K. E. Meyers

Division of Nephrology, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, USA

Search for more papers by this author
L. D. Spaneas

L. D. Spaneas

Division of Nephrology, Children's Hospital and Harvard Medical School, Boston, MA, USA

Search for more papers by this author
J. A. Palmer

J. A. Palmer

Division of Nephrology, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, USA

Search for more papers by this author
M. Salmanullah

M. Salmanullah

Division of Nephrology, Children's Hospital and Harvard Medical School, Boston, MA, USA

Search for more papers by this author
J. Baluarte

J. Baluarte

Division of Nephrology, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, USA

Search for more papers by this author
K. L. Brayman

K. L. Brayman

Department of Surgery, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, USA

Search for more papers by this author
W. E. Harmon

W. E. Harmon

Division of Nephrology, Children's Hospital and Harvard Medical School, Boston, MA, USA

Search for more papers by this author
First published: 26 March 2004
Citations: 66
Asher D. Schachter, Nephrology Division, HU-319, Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA.
Tel.: 617-355-6129
Fax: 617-232-2949
E-mail: [email protected]

Abstract

Abstract: Immunosuppression with SRL may provide an opportunity to avoid long-term exposure to the nephrotoxicity of CNI. Thus, we have initiated an experimental protocol of IL-2r antibody induction, prednisone, MMF and SRL in pediatric renal transplant recipients (median age 15.5 yr, IQR 8.5, range 1.3–21.7). The recipients were treated with daclizumab every 2 wk for the first 2 months, prednisone on a tapering schedule, MMF at 1200 mg/m2/day and SRL given b.i.d. The SRL was dosed to achieve defined target whole blood 12-h trough levels. We performed 24 SRL PK profiles in 13 stable pediatric renal transplant recipients at 1 and 3 months post-transplant. Half-life (T1/2) and terminal T1/2 were 9.7 (7.1–24.6) and 10.8 (4.4–95.2) hours (median, range) respectively at month 1, and were 9.6 (5–17.8) and 12.1 (4.7–71.0) hours respectively at month 3. SRL trough levels correlated with AUC (r2 = 0.84, p < 0.001). There was no relationship between SRL and mycophenolic acid (MPA) AUC values (r2 = 0.04). During the first 3 months post-transplant only one patient experienced severe neutropenia and another patient had subclinical (histologic) evidence of a mild acute rejection episode with no change in renal function. We conclude that the T1/2 of SRL in pediatric renal transplant recipients not treated with CNI is much shorter than what has been reported for adults, due to rapid metabolism. We conclude that children require SRL dosing every 12 h, higher doses and frequent drug monitoring to achieve target SRL concentrations.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.