1.Safety of reduced dose of mycophenolate mofetil combined with tacrolimus in living-donor liver transplantation.
Hyeyoung KIM ; Nam Joon YI ; Juyeun LEE ; Joohyun KIM ; Mi Ra MOON ; Jaehong JEONG ; Jeong Moo LEE ; Tae Suk YOU ; Suk Won SUH ; Min Su PARK ; Youngrok CHOI ; Geun HONG ; Hae Won LEE ; Kwang Woong LEE ; Kyung Suk SUH
Clinical and Molecular Hepatology 2014;20(3):291-299
BACKGROUND/AIMS: The dose of mycophenolate mofetil (MMF) has been reduced in Asia due to side effects associated with the conventional fixed dose of 2-3 g/day. We aimed to determine the pharmacokinetics of a reduced dose of MMF and to validate its feasibility in combination with tacrolimus in living-donor liver transplantation (LDLT). METHODS: Two sequential studies were performed in adult LDLT between October 2009 and 2011. First, we performed a prospective pharmacokinetic study in 15 recipients. We measured the area under the curve from 0 to 12 hours (AUC0-12) for mycophenolic acid at postoperative days 7 and 14, and we performed a protocol biopsy before discharge. Second, among 215 recipients, we reviewed 74 patients who were initially administered a reduced dose of MMF (1.0 g/day) with tacrolimus (trough, 8-12 ng/mL during the first month, and 5-8 ng/mL thereafter), with a 1-year follow-up. We performed protocol biopsies at 2 weeks and 1 year post-LDLT. RESULTS: In the first part of study, AUC0-12 was less than 30 mgh/L in 93.3% of cases. In the second, validating study, 41.9% of the recipients needed dose reduction or cessation due to side effects within the first year after LDLT. At 12 months post-LDLT, 17.6% of the recipients were administered a lower dose of MMF (0.5 g/day), and 16.2% needed permanent cessation due to side effects. The 1- and 12-month rejection-free survival rates were 98.6% and 97.3%, respectively. CONCLUSIONS: A reduced dose of MMF was associated with low blood levels compared to the existing recommended therapeutic range. However, reducing the dose of MMF combined with a low level of tacrolimus was feasible clinically, with an excellent short-term outcome in LDLT.
Adult
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Aged
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Area Under Curve
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Drug Therapy, Combination
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Female
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Follow-Up Studies
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Gastrointestinal Diseases/etiology
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Graft Rejection/prevention & control
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Humans
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Immunosuppressive Agents/blood/*pharmacokinetics
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Leukopenia/etiology
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Liver/pathology
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Liver Failure/*therapy
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*Liver Transplantation
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Male
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Middle Aged
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Mycophenolic Acid/adverse effects/*analogs & derivatives/blood/pharmacokinetics
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ROC Curve
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Retrospective Studies
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Tacrolimus/therapeutic use
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Tissue Donors