Pharmacokinetics of CsA during the switch from continuous intravenous infusion to oral administration after allogeneic hematopoietic stem cell transplantation

We investigated the serial changes in the blood CsA concentration during the switch from continuous intravenous infusion to twice-daily oral administration in allogeneic hematopoietic stem cell transplant recipients (n=12). The microemulsion form of CsA, Neoral, was started at twice the last dose in intravenous infusion in two equally divided doses. The area under the concentration–time curve during oral administration (AUCPO) was significantly higher than the AUC during intravenous infusion (AUCIV) (median 7508 vs 6705 ng/ml × h, P=0.050). The median bioavailability of Neoral, defined as (AUCPO/DOSEPO) divided by (AUCIV/DOSEIV), was 0.685 (range, 0.45–1.04). Concomitant administration of oral voriconazole (n=4) significantly increased the bioavailability of Neoral (median 0.87 vs 0.54, P=0.017), probably due to the inhibition of gut CYP3A4 by voriconazole. Although the conversion from intravenous to oral administration of CsA at a ratio of 1:2 seemed to be appropriate in most patients, a lower conversion ratio may be better in patients taking oral voriconazole. To obtain a similar AUC, the target trough concentrations during twice-daily oral administration should be halved compared with the target concentration during continuous infusion.

[1]  B. Wolf,et al.  Measurement of cyclosporine concentrations in whole blood: HPLC and radioimmunoassay with a specific monoclonal antibody and 3H- or 125I-labeled ligand compared. , 1989, Clinical chemistry.

[2]  B. Carleton,et al.  INTERACTION BETWEEN CYCLOSPORINE AND FLUCONAZOLE IN RENAL ALLOGRAFT RECIPIENTS , 1991, Transplantation.

[3]  J. López-Gil,et al.  Fluconazole-Cyclosporine Interaction: A Dose-Dependent Effect? , 1993, The Annals of pharmacotherapy.

[4]  J. Kovarik,et al.  The pharmacokinetics of Sandimmun Neoral: a new oral formulation of cyclosporine. , 1994, Transplantation proceedings.

[5]  E D Thomas,et al.  1994 Consensus Conference on Acute GVHD Grading. , 1995, Bone marrow transplantation.

[6]  J. Wingard,et al.  Evaluation of the drug interaction between intravenous high-dose fluconazole and cyclosporine or tacrolimus in bone marrow transplant patients. , 1996, Transplantation.

[7]  A. Gratwohl,et al.  A survey of the prophylaxis and treatment of acute GVHD in Europe: a report of the European Group for Blood and Marrow Transplantation (EBMT) , 1997, Bone Marrow Transplantation.

[8]  E. Milgalter,et al.  Dose adjustment and cost of itraconazole prophylaxis in lung transplant recipients receiving cyclosporine and tacrolimus (FK 506). , 1997, Transplantation proceedings.

[9]  D. Min,et al.  Effect of Grapefruit Juice on the Pharmacokinetics of Microemulsion Cyclosporine and its Metabolite in Healthy Volunteers: Does the Formulation Difference Matter? , 1998, Journal of clinical pharmacology.

[10]  J. Spence,et al.  Pharmacokinetic-Pharmacodynamic Consequences and Clinical Relevance of Cytochrome P450 3A4 Inhibition , 2000, Clinical pharmacokinetics.

[11]  H. Esperou,et al.  New oral formulation of cyclosporin A (Neoral) pharmacokinetics in allogeneic bone marrow transplant recipients , 2000, Bone Marrow Transplantation.

[12]  S. Mineishi,et al.  Pre-emptive therapy against cytomegalovirus (CMV) disease guided by CMV antigenemia assay after allogeneic hematopoietic stem cell transplantation: a single-center experience in Japan , 2001, Bone Marrow Transplantation.

[13]  D. Nicolau,et al.  Beneficial pharmacokinetic interaction between cyclosporine and itraconazole in renal transplant recipients. , 2003, Transplantation proceedings.

[14]  H. Leather Drug interactions in the hematopoietic stem cell transplant (HSCT) recipient: what every transplanter needs to know , 2004, Bone Marrow Transplantation.

[15]  K. Oka,et al.  Evaluation of appropriate blood level in continuous intravenous infusion from trough concentrations after oral administration based on area under trough level in tacrolimus and cyclosporine therapy. , 2005, Transplantation proceedings.

[16]  J. Wingard,et al.  Pharmacokinetic evaluation of the drug interaction between intravenous itraconazole and intravenous tacrolimus or intravenous cyclosporin A in allogeneic hematopoietic stem cell transplant recipients. , 2006, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[17]  Y. Kanda,et al.  Effect of blood cyclosporine concentration on the outcome of hematopoietic stem cell transplantation from an HLA‐matched sibling donor , 2006, American journal of hematology.

[18]  R. Yamazaki,et al.  Greater impact of oral fluconazole on drug interaction with intravenous calcineurin inhibitors as compared with intravenous fluconazole , 2007, European Journal of Clinical Pharmacology.

[19]  H. Nakasone,et al.  Decreased incidence of acute graft‐versus‐host disease by continuous infusion of cyclosporine with a higher target blood level , 2008, American journal of hematology.

[20]  H. Nakasone,et al.  Long‐term ultra‐low‐dose acyclovir against varicella‐zoster virus reactivation after allogeneic hematopoietic stem cell transplantation , 2007, American journal of hematology.

[21]  Jun Kato,et al.  Drug interaction between voriconazole and calcineurin inhibitors in allogeneic hematopoietic stem cell transplant recipients , 2009, Bone Marrow Transplantation.

[22]  H. Nakasone,et al.  Fludarabine, cyclophosphamide, anti‐thymocyteglobulin, and low‐dose total body irradiation conditioning enables 1‐HLA‐locus‐mismatched hematopoietic stem cell transplantation for very severe aplastic anemia without affecting ovarian function , 2009, American journal of hematology.