TY - JOUR
T1 - Mycophenolate monitoring in liver, thoracic, pancreas, and small bowel transplantation
T2 - A consensus report
AU - Cantarovich, Marcelo
AU - Brown, Nigel W.
AU - Ensom, Mary H.H.
AU - Jain, Ashok
AU - Kuypers, Dirk R.J.
AU - Gelder, Teun Van
AU - Tredger, J. Michael
N1 - Funding Information:
M.C. was a recipient of Educational Grants (Astellas, Hoffman LaRoche, Genzyme, Novartis, Wyeth), Research Grant (Astellas), and on Advisory Boards (Astellas, Novartis, Hoffman LaRoche). M.H.H.E. received unrestricted grants from Hoffman-La Roche, Ltd . D.R.K. received travel fees, honoraria, and grants from Hoffman-La Roche and travel fees and honoraria from Novartis . T.V.G. has received lecture fees and research support from Hoffman-La Roche. J.M.T. has received a travel grant from Astellas . N.W.B. and A.J. declare no conflicts of interest.
PY - 2011/4
Y1 - 2011/4
N2 - Assessing the value of mycophenolic acid (MPA) monitoring outside renal transplantation is hindered by the absence of any trial comparing fixed-dose and concentration-controlled therapy. However, in liver and thoracic transplantation particularly, clinical trials, observational studies with comparison groups, and case series have described MPA efficacy, exposure/efficacy relationships, pharmacokinetic variability, and clinical outcomes relating to plasma MPA concentrations. On the basis of this evidence, this report identifies MPA as an immunosuppressant for which the combination of variable disposition, efficacy, and adverse effects contributes to interindividual differences seemingly in excess of those optimal for a fixed-dosage mycophenolate regimen. Combined with experiences of MPA monitoring in other transplant indications, the data have been rationalized to define circumstances in which measurement of MPA concentrations can contribute to improved management of mycophenolate therapy in nonrenal transplant recipients.
AB - Assessing the value of mycophenolic acid (MPA) monitoring outside renal transplantation is hindered by the absence of any trial comparing fixed-dose and concentration-controlled therapy. However, in liver and thoracic transplantation particularly, clinical trials, observational studies with comparison groups, and case series have described MPA efficacy, exposure/efficacy relationships, pharmacokinetic variability, and clinical outcomes relating to plasma MPA concentrations. On the basis of this evidence, this report identifies MPA as an immunosuppressant for which the combination of variable disposition, efficacy, and adverse effects contributes to interindividual differences seemingly in excess of those optimal for a fixed-dosage mycophenolate regimen. Combined with experiences of MPA monitoring in other transplant indications, the data have been rationalized to define circumstances in which measurement of MPA concentrations can contribute to improved management of mycophenolate therapy in nonrenal transplant recipients.
UR - http://www.scopus.com/inward/record.url?scp=79953720823&partnerID=8YFLogxK
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U2 - 10.1016/j.trre.2010.12.001
DO - 10.1016/j.trre.2010.12.001
M3 - Review article
C2 - 21454066
AN - SCOPUS:79953720823
SN - 0955-470X
VL - 25
SP - 65
EP - 77
JO - Transplantation Reviews
JF - Transplantation Reviews
IS - 2
ER -