Combined approach with therapeutic drug monitoring and pharmacogenomics in renal transplant recipients

Introduction

Tacrolimus-based regimen that includes induction with daclizumab and maintenance with mycophenolate mofetil and corticosteroids has superior efficacy in renal transplantation when compared with cyclosporine-based regimens.[12] Pharmacodynamic and pharmacokinetic variability with tacrolimus have been attributed to various factors such as co-medication, biochemical, hematological parameters, and genetic constitution.[34] Dose individualization for tacrolimus is routinely achieved with therapeutic drug monitoring. Recent literature highlights personalizing drug therapy using the pharmacogenomic approach.[5]

Inter-individual variability of tacrolimus is attributed to polymorphisms of Cyp3A5 and transporters as P glycoprotein.[67] The presence of Cyp3A5*3 allele, CYP3A5*6, or MDR-1 (T-1236C, C3435T, and G2677T) are associated with an increased exposure to tacrolimus. Scholten et al. reported that tacrolimus area under the concentration time curve (AUC_0-12) of 210 ng.h/mL for 6 weeks post-transplant and 125 ng.h/mL thereafter would be adequate to prevent acute rejections.[8] For mycophenolate, the dosing is based on maintaining AUC_0-12 within 30-60 mg.h/L.[9]

Case Report

A 50-year-old lady of mongoloid extraction from Bhutan, with chronic kidney disease resulting from membranous proliferative glomerulonephritis pre-emptively received a renal allograft from her haplo-matched cousin sister. Her pre-transplant donor-recipient crossmatch and donor-specific antibodies were negative. She received standard immunosuppressive therapy with mycophenolate sodium (1440 mg/day), tacrolimus (5.5 mg/day), and steroid (20 mg/day) with basiliximab induction. She was also prescribed valganciclovir, cotrimoxazole, pantoprazole, and calcium. During the first 2 months post-transplant the MPA AUC_0-12 ranged from 29.2 to 168.7 mg.h/L with total daily doses varying from 1440 to 1620 mg. She developed leukopenia which did not remit with reduction in dose of mycophenolate. Due to persistent leucopenia, other drugs such as valganciclovir and co-trimoxazole were stopped. Mycophenolate dose was gradually tapered but leucopenia continued to worsen therefore mycophenolate was stopped. Subsequently, leucocyte counts never increased more than 5000/cu.mm so mycophenolate could not be restarted. Renal and liver function parameters were within normal limits in the post-transplant period. The tacrolimus trough measurements (ng/ml) and the subsequent dose adjustments over time are shown in Figure 1.

Close

Figure 1

Tacrolimus dose (mg/kg) and trough measurements (ng/mL) over time

Export to PPT

Dose reductions for tacrolimus were made gradually over a 1½ month period. However, the trough concentration remained above the recommended trough concentration. Tacrolimus 2 point LSS AUC within the first post-transplant year ranged between 165.6 and 140.9 μg.h/L while on 2 mg/day in two divided doses, which was within the range of exposure in the maintenance period at this center.[10] Post-transplant immune monitoring with donor-specific antibody was negative throughout her follow-up. BK virus PCR screening remained negative when tested during serial visits.

Two years later, the two-point LSS tacrolimus AUC increased to 281.7 μg.h/L after initiation of ciprofloxacin which reduced to 217.3 μg.h/L, 1 week after discontinuation of ciprofloxacin.

In view of the possibility of polymorphism affecting tacrolimus metabolism, with informed consent, single nucleotide polymorphisms that could account for the elevated tacrolimus levels were tested for with PCR. She was mutant homozygous for CYP3A5*3(GG) alleles and MDR1-2677(TT) alleles, heterozygous for MDR1-1236(CT) alleles and wild-type homozygous for CYP3A5*6 (GG) and MDR1 3435C (CC) alleles.

Discussion

The optimum therapeutic range of tacrolimus trough concentrations in our transplant unit for the immunosuppressive regimen with MPA, tacrolimus, and steroid is 5-10 ng/mL for the 1^st month after transplantation and 3-5 ng/mL thereafter, provided there is no evidence of rejection. Unlike other transplant patients, this patient was maintained on an immunosuppressive regimen of only tacrolimus and prednisolone, but at significantly higher tacrolimus trough concentrations than normal after stabilization (7-20 ng/mL). There were no clinical features of side effects including tremor or biochemical features of rejection or toxicity.

Mutations in the genes encoding for CYP3A5 and MDR 1 (2677G > T) explains the increased exposure to tacrolimus. The availability of this information in the early treatment period could have decreased the number of TDM specimens and if in future patients with this genotype can be managed on low doses of tacrolimus alone it will significantly reduce the cost of treatment. TDM is the proven cornerstone of dose individualization but pharmacogenomics has a vital role to play. In South Indians the frequency of CYP3A5*3 was found to be 63.5% which is significantly different from the incidence among the African Americans, Caucasians (87.3%), and Chinese population.[11]

Conclusion

This case report gives rise to a number of questions. Can other patients with this genotype be maintained on only low dose tacrolimus with steroids? Will a mandatory genetic screening of patients undergoing renal transplant reduce the overall cost and time to individualized therapy? Would it be necessary to define a different tacrolimus trough therapeutic range for patients maintained on only two drug immunosuppressive regimen (tacrolimus + steroid).