TY - JOUR
T1 - A systematic literature review approach to estimate the therapeutic index of selected immunosuppressant drugs after renal transplantation
AU - Ericson, Jessica E.
AU - Zimmerman, Kanecia O.
AU - Gonzalez, Daniel
AU - Melloni, Chiara
AU - Guptill, Jeffrey T.
AU - Hill, Kevin D.
AU - Wu, Huali
AU - Cohen-Wolkowiez, Michael
N1 - Funding Information:
Supported by the Food and Drug Administration through Grants 1U01FD004858-01 and 3U01FD004858-01. J. E. Ericson received support from the NICHD under award number 5T32HD060558. K. O. Zimmerman is funded by KL2TR001115-03 from the Duke Clinical and Translational Science Awards. D. Gonzalez is funded by K23HD083465 from the National Institute for Child Health and Human Development (NICHD) and by the nonprofit Thrasher Research Fund (www.thrasherresearch.org). C. Melloni receives support for research from the NICHD (HHSN275201000003I), the FDA (3U01FD004858-01), and from industry for drug development in adults (www.dcri.duke.edu/ research/coi.jsp). J. T. Guptill is supported by K23NS085049-01A1 from National Institute of Neurological Disorders and Stroke (NINDS), the Myasthenia Gravis Foundation of America, the NICHD (HHSN275201000003I), and from industry for drug development in adults (www.dcri.duke.edu/research/coi.jsp). K. D. Hill is supported in part by grants from The National Center for Advancing Translational Sciences of the National Institutes of Health (KL2TR001115-02), the Mend A Heart Foundation (Clarendon Hills, IL), and from industry (Gilead Sciences and Kowa pharmaceuticals) for drug development in children. M. Cohen-Wolkowiez receives support for research from the NIH (1R01-HD076676-01A1), the National Center for Advancing Translational Sciences of the NIH (UL1TR001117), the NIAID (HHSN272201500006I and HHSN272201300017I), the NICHD (HHSN275201000003I), the FDA (1U01FD004858-01), the Biomedical Advanced Research and Development Authority (HHSO100201300009C), the nonprofit Thrasher Research Fund (www.thrasherresearch.org), and from the industry for drug development in adults and children (www.dcri.duke.edu/research/coi.jsp). The remaining author declares no conflict of interest.
Publisher Copyright:
Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2017
Y1 - 2017
N2 - Background: Drugs that exhibit close margins between therapeutic and toxic blood concentrations are considered to have a narrow therapeutic index (NTI). The Food and Drug Administration has proposed that NTI drugs should have more stringent bioequivalence standards for approval of generic formulations. However, many immunosuppressant drugs do not have a well-defined therapeutic index (TI). Methods: We sought to determine whether safety, efficacy, and pharmacokinetic data obtained from the medical literature through a comprehensive literature search could be used to estimate the TI of cyclosporine, tacrolimus, and sirolimus. In this analysis, we considered TI ≤2 as a criterion to define a drug as having an NTI. Results: Published literature indicates that cyclosporine has a TI of 2-3, which falls just short of our criteria to be classified as having an NTI. We found sirolimus and tacrolimus to have a therapeutic range of 5-12 ng/mL and of 5-20 ng/mL, respectively, but were unable to calculate the TI. Conclusions: Although the current literature does not provide a clear indication that these drugs have an NTI, the routine use of therapeutic drug monitoring in clinical practice suggests that more stringent testing of their pharmacokinetic and pharmacodynamic properties should be performed before the approval of generic formulations.
AB - Background: Drugs that exhibit close margins between therapeutic and toxic blood concentrations are considered to have a narrow therapeutic index (NTI). The Food and Drug Administration has proposed that NTI drugs should have more stringent bioequivalence standards for approval of generic formulations. However, many immunosuppressant drugs do not have a well-defined therapeutic index (TI). Methods: We sought to determine whether safety, efficacy, and pharmacokinetic data obtained from the medical literature through a comprehensive literature search could be used to estimate the TI of cyclosporine, tacrolimus, and sirolimus. In this analysis, we considered TI ≤2 as a criterion to define a drug as having an NTI. Results: Published literature indicates that cyclosporine has a TI of 2-3, which falls just short of our criteria to be classified as having an NTI. We found sirolimus and tacrolimus to have a therapeutic range of 5-12 ng/mL and of 5-20 ng/mL, respectively, but were unable to calculate the TI. Conclusions: Although the current literature does not provide a clear indication that these drugs have an NTI, the routine use of therapeutic drug monitoring in clinical practice suggests that more stringent testing of their pharmacokinetic and pharmacodynamic properties should be performed before the approval of generic formulations.
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U2 - 10.1097/FTD.0000000000000364
DO - 10.1097/FTD.0000000000000364
M3 - Review article
C2 - 28081041
AN - SCOPUS:85010422720
SN - 0163-4356
VL - 39
SP - 13
EP - 20
JO - Therapeutic Drug Monitoring
JF - Therapeutic Drug Monitoring
IS - 1
ER -