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Assessment of converting from intravenous to oral administration of cyclosporin A in pediatric allogeneic hematopoietic stem cell transplant recipients

Authors
Choi, J. S.Lee, S. H.Chung, S. J.Yoo, K. H.Sung, K. W.Koo, H. H.
Issue Date
Jul-2006
Publisher
NATURE PUBLISHING GROUP
Keywords
pharmacokinetic; cyclosporin A; hematopoietic stem cell transplantation; pediatric
Citation
BONE MARROW TRANSPLANTATION, v.38, no.1, pp 29 - 35
Pages
7
Journal Title
BONE MARROW TRANSPLANTATION
Volume
38
Number
1
Start Page
29
End Page
35
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/15111
DOI
10.1038/sj.bmt.1705402
ISSN
0268-3369
1476-5365
Abstract
We studied the administration method during a transition period from continuous intravenous ( i.v.) infusion to oral administration of cyclosporin A ( CsA). Thirty-two pediatric hematopoietic stem cell transplant ( HSCT) recipients, between the ages of 8 months and 15.6 years ( median 7.1 years) participated in this study. The pharmacokinetic properties of CsA was evaluated during the transition period from i.v. to oral CsA. The daily oral dose of CsA was three times higher than the i.v. dose. Oral dosing began immediately after the continuous infusion was discontinued. Whole-blood CsA concentrations were measured by a monoclonal fluorescence polarization immunoassay ( FPIA). The mean +/- s.d. value of bioavailability ( F), maximum concentration ( C-max), half-life ( t(1/2)) of CsA were 43.1 +/- 14.4%, 1135.3 +/- 340.6 ng/ml and 3.1 +/- 1.2 h, respectively. Mean clearance ( CL)+/- s.d. was 480.9 +/- 103.7, 414.9 +/- 137.1 and 320 +/- 51.8 ml/h/kg in patients < 20, 20-40 and 440 kg of body weight, respectively. The CsA CL of younger children was significantly greater than for older children ( P = 0.044). CsA trough levels were maintained within the therapeutic range throughout the transition period. Therefore, our findings suggest that the immediate administration of an oral formulation, after discontinuation of the continuous infusion, would be practical and effective for routine clinical use.
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