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

被引:14
作者
Choi, J. S.
Lee, S. H.
Chung, S. J.
Yoo, K. H.
Sung, K. W.
Koo, H. H.
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol & Oncol,Dept Pediat, Seoul, South Korea
[2] Samsung Med Ctr, Div Pharmaceut Serv, Seoul, South Korea
[3] Sookmyung Womens Univ, Grad Sch Clin Pharm, Seoul, South Korea
[4] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
关键词
pharmacokinetic; cyclosporin A; hematopoietic stem cell transplantation; pediatric;
D O I
10.1038/sj.bmt.1705402
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:29 / 35
页数:7
相关论文
共 43 条
[1]   Management of graft-versus-host disease [J].
Arai, S ;
Vogelsang, GB .
BLOOD REVIEWS, 2000, 14 (04) :190-204
[2]  
ATKINSON K, 1984, BRIT J HAEMATOL, V56, P223, DOI 10.1111/j.1365-2141.1984.tb03950.x
[3]  
ATKINSON K, 1987, BONE MARROW TRANSPL, V1, P265
[4]  
BLIFELD C, 1987, NEW ENGL J MED, V317, P509
[5]  
BURCKART G, 1985, TRANSPLANT P, V17, P1172
[6]   CYCLOSPORINE ABSORPTION FOLLOWING ORTHOTOPIC LIVER-TRANSPLANTATION [J].
BURCKART, GJ ;
VENKATARAMANAN, R ;
PTACHCINSKI, RJ ;
STARZL, TE ;
GARTNER, JC ;
ZITELLI, BJ ;
MALATACK, JJ ;
SHAW, BW ;
IWATSUKI, S ;
VANTHIEL, DH .
JOURNAL OF CLINICAL PHARMACOLOGY, 1986, 26 (08) :647-651
[7]   MONITORING OF CYCLOSPORINE BLOOD-LEVELS FROM CENTRAL VENOUS LINES - A MISLEADING ASSAY [J].
BUSCA, A ;
MINIERO, R ;
VASSALLO, E ;
LEONE, L ;
ODDENINO, O ;
MADON, E .
THERAPEUTIC DRUG MONITORING, 1994, 16 (01) :71-74
[8]  
CARRERAS E, 1988, BONE MARROW TRANSPL, V3, P637
[9]  
Caudell K A, 1990, Oncol Nurs Forum, V17, P563
[10]   CYCLOSPORINE, METHOTREXATE, AND PREDNISONE COMPARED WITH CYCLOSPORINE AND PREDNISONE FOR PROPHYLAXIS OF ACUTE GRAFT-VERSUS-HOST DISEASE [J].
CHAO, NJ ;
SCHMIDT, GM ;
NILAND, JC ;
AMYLON, MD ;
DAGIS, AC ;
LONG, GD ;
NADEMANEE, AP ;
NEGRIN, RS ;
ODONNELL, MR ;
PARKER, PM ;
SMITH, EP ;
SNYDER, DS ;
STEIN, AS ;
WONG, RM ;
BLUME, KG ;
FORMAN, SJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (17) :1225-1230