A rational dosing algorithm for basiliximab (simulect) in pediatric renal transplantation based on pharmacokinetic-dynamic evaluations

John M. Kovarik, Gisela Offner, Michel Broyer, Patrick Niaudet, Chantal Loirat, Mark Mentser, Jacques Lemire, John F.S. Crocker, Pierre Cochat, Godfrey Clark, Christophe Gerbeau, Lawrence Chodoff, Alexander Korn, Michael Hall

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

49 Citas (Scopus)

Resumen

Background. The pharmacokinetics and immunodynamics of basiliximab were assessed in 39 pediatric de novo kidney allograft recipients to rationally chose a dose regimen for this age group. Methods. In study part 1, patients were given 12 mg/m2 of basiliximab by bolus intravenous injection before surgery and on day 4. An interim pharmacokinetic evaluation supported a fixed-dose approach for study part 2 in which infants and children received two 10-mg doses and adolescents received two 20-mg doses. Blood samples were collected over a 12-week period for analysis of basiliximab and soluble interleukin-2 receptor concentrations, flow cytometry, and screening for anti-idiotype antibodies. Results. Basiliximab clearance in infants and children (n=25) was reduced by approximately half compared with adults from a previous study and was independent of age (1-11 years), weight (9-37 kg), and body surface area (0.44-1.20 m2). Clearance in adolescents (12-16 years, n= 14) approached or reached adult values. CD25-saturating basiliximab concentrations were maintained for 31±12 days in study part 1 with mg/m2 dosing and for 36±14 days in study part 2 based on the fixed-dose regimen (P=0.31). A single patient experienced a rejection episode during CD25 saturation. The duration of CD25 saturation in patients who experienced a rejection episode after desaturation did not differ from those who remained rejection-free for the full 6-month period: 34±6 days (n=6) vs. 35±14 days (n=33 patients); P=0.74. Anti-idiotype antibodies were detected in two patients; however, this did not influence the clearance of basiliximab or the duration of CD25 saturation. Conclusions. To achieve similar basiliximab exposure as is efficacious in adults, pediatric patients <35 kg should receive two 10-mg doses and those ≥35 kg should receive two 20-mg doses of basiliximab by intravenous infusion or bolus injection. The first dose is given before surgery and the second on day 4 after transplantation.

Idioma originalEnglish
Páginas (desde-hasta)966-971
Número de páginas6
PublicaciónTransplantation
Volumen74
N.º7
DOI
EstadoPublished - oct. 15 2002
Publicado de forma externa

ASJC Scopus Subject Areas

  • Transplantation

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Kovarik, J. M., Offner, G., Broyer, M., Niaudet, P., Loirat, C., Mentser, M., Lemire, J., Crocker, J. F. S., Cochat, P., Clark, G., Gerbeau, C., Chodoff, L., Korn, A., & Hall, M. (2002). A rational dosing algorithm for basiliximab (simulect) in pediatric renal transplantation based on pharmacokinetic-dynamic evaluations. Transplantation, 74(7), 966-971. https://doi.org/10.1097/00007890-200210150-00011