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

被引:23
作者
Luis Pinana, Jose [1 ,2 ,3 ]
Perez-Pitarch, Alejandro [4 ]
Guglieri-Lopez, Beatriz [5 ]
Gimenez, Estela [6 ]
Carlos Hernandez-Boluda, Juan [1 ]
Jose Terol, Maria [1 ]
Ferriols-Lisart, Rafael [4 ]
Solano, Carlos [1 ,7 ]
Navarro, David [6 ,8 ]
机构
[1] Hosp Clin Univ, Dept Hematol, Fdn Invest, INCLIVA, Valencia, Spain
[2] Hosp Univ & Politecn la Fe, Dept Hematol, Valencia, Spain
[3] Inst Carlos III, CIBERONC, Madrid, Spain
[4] Hosp Clin Univ, Dept Pharm, Valencia, Spain
[5] Hosp Univ Doctor Peset, Dept Pharm, Valencia, Spain
[6] Hosp Clin Univ, Microbiol Serv, Valencia, Spain
[7] Univ Valencia, Sch Med, Dept Med, Valencia, Spain
[8] Univ Valencia, Sch Med, Dept Microbiol, Valencia, Spain
关键词
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; HOST-DISEASE PROPHYLAXIS; DELTA T-CELLS; MARIBAVIR PROPHYLAXIS; DOUBLE-BLIND; INFECTION; RECIPIENTS; TACROLIMUS/SIROLIMUS; ERA; PREVENTION; MORTALITY;
D O I
10.1111/ajt.14754
中图分类号
R61 [外科手术学];
学科分类号
摘要
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.
引用
收藏
页码:2885 / 2894
页数:10
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