4.6 Article

Sirolimus exposure and the occurrence of cytomegalovirus DNAemia after allogeneic hematopoietic stem cell transplantation

Journal

AMERICAN JOURNAL OF TRANSPLANTATION
Volume 18, Issue 12, Pages 2885-2894

Publisher

WILEY
DOI: 10.1111/ajt.14754

Keywords

antibiotic: antiviral; basic (laboratory) research/science; bone marrow/hematopoietic stem cell transplantation; clinical research/practice; immunosuppressant-calcineurin inhibitor: tacrolimus; immunosuppressant-mechanistic target of rapamycin: sirolimus; infection and infectious agents-viral: cytomegalovirus (CMV); infectious disease; pharmacokinetics/pharmacodynamics; pharmacology

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Sirolimus appears to protect against cytomegalovirus (CMV) in organ transplant recipients. The effect of this drug in allogeneic hematopoietic stem cell transplantation recipients remains unexplored. By means of multivariate continuous-time Markov model analyses, we identified 3 independent covariates that significantly impacted the risk of CMV DNAemia: recipient/donor CMV serostatus, tacrolimus exposure, and sirolimus exposure. CMV-seropositive recipients with CMV-seronegative donors had a significantly higher probability of having detectable CMV DNAemia. Increasing the tacrolimus trough concentration from 0 to 16 ng/mL increased the probability of patients having detectable CMV DNAemia by 40% (from 40% to 80%), whereas this probability decreased by 25% (from 40% to 15%) when trough concentrations of sirolimus increased from 0 to 16 ng/mL. Sensitivity analysis showed that sirolimus exposure between 0 and 6 ng/mL has no or negligible effect on CMV DNAemia, but levels >8 ng/mL significantly decreased the number of detectable CMV DNAemia cases (the risk ratios decreased from 0.68 to 0.21 when whole blood sirolimus concentrations changed from 8 to 18 ng/mL, P < .01). In conclusion, we used a pharmacometric statistical tool to provide the first clinical evidence that fewer CMV DNAemia events become detectable as sirolimus exposure increases.

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