TY - JOUR
T1 - Effect of Sirolimus Exposure on the Need for Preemptive Antiviral Therapy for Cytomeglovirus Infection after Allogeneic Hematopoietic Stem Cell Transplantation
AU - Guglieri-Lopez, Beatriz
AU - Perez-Pitarch, Alejandro
AU - Garcia-Cadenas, Irene
AU - Gimenez, Estela
AU - Barba, Pere
AU - Rabella, Nuria
AU - Hernandez-Boluda, Juan Carlos
AU - Fox, Laura
AU - Valcarcel, David
AU - Esquirol, Albert
AU - Ferriols-Lisart, Rafael
AU - Sierra, Jorge
AU - Solano, Carlos
AU - Navarro, David
AU - Martino, Rodrigo
AU - Piñana, José Luis
PY - 2019/5/1
Y1 - 2019/5/1
N2 - © 2019 American Society for Blood and Marrow Transplantation The current study evaluates the clinical effect of sirolimus exposure on the occurrence of cytomegalovirus (CMV)DNAemia necessitating preemptive antiviral therapy. A total of 167 consecutive recipients of reduced-intensity conditioning (RIC)allogeneic hematopoietic stem cell transplantation (allo-HSCT)who received sirolimus- and tacrolimus-based graft-versus-host disease (GVHD)prophylaxis and whose CMV serostatus was positive for donors and/or recipients were included in this multicenter retrospective study. A parametric model with consecutive sirolimus blood levels describing the time to CMV DNAemia-RAT was developed using NONMEM version 7.4. Overall, 122 of 167 patients (73%)were allografted from an unrelated donor, and the donor CMV-serostatus was negative in 51 cases (31%). Fifty-six recipients (34%)developed CMV DNAemia necessitating preemptive therapy, with a cumulative incidence of 36% at a median follow-up of 25 months. Time to CMV DNAemia necessitating preemptive therapy was best described using a Gompertz function. CMV DNAemia necessitating preemptive therapy-predicting factors were antithymocyte globulin-based conditioning regimen (hazard ratio [HR], 2.2; 95% confidence interval [CI], 1.1 to 4.1; P <.01)and sirolimus concentration (HR,.94; 95% CI,.87 to.99; P <.01). The risk of CMV DNAemia-RAT decreased by 6% for each 1 ng/mL increase in sirolimus trough concentration. In conclusion, we provide evidence on the association between sirolimus blood concentration and incidence of CMV DNAemia necessitating preemptive therapy in allo-HSCT recipients. Moreover, this study presents the first predictive model describing the time to CMV DNAemia necessitating preemptive antiviral therapy as a function of sirolimus drug concentration.
AB - © 2019 American Society for Blood and Marrow Transplantation The current study evaluates the clinical effect of sirolimus exposure on the occurrence of cytomegalovirus (CMV)DNAemia necessitating preemptive antiviral therapy. A total of 167 consecutive recipients of reduced-intensity conditioning (RIC)allogeneic hematopoietic stem cell transplantation (allo-HSCT)who received sirolimus- and tacrolimus-based graft-versus-host disease (GVHD)prophylaxis and whose CMV serostatus was positive for donors and/or recipients were included in this multicenter retrospective study. A parametric model with consecutive sirolimus blood levels describing the time to CMV DNAemia-RAT was developed using NONMEM version 7.4. Overall, 122 of 167 patients (73%)were allografted from an unrelated donor, and the donor CMV-serostatus was negative in 51 cases (31%). Fifty-six recipients (34%)developed CMV DNAemia necessitating preemptive therapy, with a cumulative incidence of 36% at a median follow-up of 25 months. Time to CMV DNAemia necessitating preemptive therapy was best described using a Gompertz function. CMV DNAemia necessitating preemptive therapy-predicting factors were antithymocyte globulin-based conditioning regimen (hazard ratio [HR], 2.2; 95% confidence interval [CI], 1.1 to 4.1; P <.01)and sirolimus concentration (HR,.94; 95% CI,.87 to.99; P <.01). The risk of CMV DNAemia-RAT decreased by 6% for each 1 ng/mL increase in sirolimus trough concentration. In conclusion, we provide evidence on the association between sirolimus blood concentration and incidence of CMV DNAemia necessitating preemptive therapy in allo-HSCT recipients. Moreover, this study presents the first predictive model describing the time to CMV DNAemia necessitating preemptive antiviral therapy as a function of sirolimus drug concentration.
KW - Allogeneic hematopoietic stem cells transplantation
KW - Cytomegalovirus disease
KW - Cytomegalovirus DNAemia
KW - Cytomegalovirus infection
KW - Mechanistic target of rapamycin inhibitor
KW - PK/PD
KW - Preemptive antiviral therapy
KW - Quantitative PCR
KW - Sirolimus
KW - Sirolimus exposure
KW - Time-to-event analysis
UR - http://www.mendeley.com/research/effect-sirolimus-exposure-need-preemptive-antiviral-therapy-cytomeglovirus-infection-after-allogenei
U2 - 10.1016/j.bbmt.2019.01.012
DO - 10.1016/j.bbmt.2019.01.012
M3 - Article
C2 - 30639821
SN - 1083-8791
VL - 25
SP - 1022
EP - 1030
JO - Biology of Blood and Marrow Transplantation
JF - Biology of Blood and Marrow Transplantation
ER -