| Literature DB >> 29603596 |
José Luis Piñana1,2,3, Alejandro Perez-Pitarch4, Beatriz Guglieri-Lopez5, Estela Giménez6, Juan Carlos Hernandez-Boluda1, María José Terol1, Rafael Ferriols-Lisart4, Carlos Solano1,7, David Navarro6,8.
Abstract
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.Entities:
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
Year: 2018 PMID: 29603596 DOI: 10.1111/ajt.14754
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086