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Association of Baseline Viral Serology and Sirolimus Regimens With Kidney Transplant Outcomes: A 14-Year Registry-Based Cohort Study in the United States.
- Source :
-
Transplantation [Transplantation] 2017 Feb; Vol. 101 (2), pp. 377-386. - Publication Year :
- 2017
-
Abstract
- Background: The risks for transplant outcomes associated with baseline viral serostatus in kidney transplant recipients (KTR) on sirolimus have not been widely studied.<br />Methods: We performed a cohort-study of 61 590 adult KTR in 2000 to 2013. We used Cox regression models to determine the adjusted hazard ratio (aHR) of patient death, death-censored graft loss and posttransplant malignancy associated with the baseline serostatus (+ or -: hepatitis B core [HBc], hepatitis C virus [HCV], Epstein-Barr virus [EBV], or cytomegalovirus [CMV]) in KTR on sirolimus (SRL) + mycophenolate (MPA) or SRL + tacrolimus (Tac), relative to the control-regimen: Tac + MPA.<br />Results: Compared with Tac + MPA, SRL + MPA, and SRL + Tac were associated with higher risks of 5-year mortality (aHR, 1.41; 95% CI, 1.23-1.60 and aHR, 1.59; 95% CI, 1.38-1.83, respectively) and death-censored graft loss (aHR, 1.41; 95% CI, 1.24-1.60 and aHR, 1.38; 95% CI, 1.21-1.57, respectively). In KTR with negative pretransplant EBV, CMV, HBc, or HCV serostatus, SRL + MPA not SRL + Tac was associated with a lower risk of posttransplant malignancy compared with control (aHR, 0.27; 95% CI, 0.10-0.72; aHR, 0.61; 95% CI, 0.43-0.88; aHR, 0.79; 95% CI, 0.64-0.97; and aHR, 0.80; 95% CI, 0.65-0.98, respectively, for SRL + MPA and aHR, 0.98: 95% CI, 0.52-1.80; aHR, 0.69; 95% CI, 0.46-1.06; aHR, 0.83; 95% CI, 0.66-1.06 and aHR, 0.85; 95% CI, 0.67-1.07, respectively, for SRL + Tac). In KTR with positive serostatus to any of the above viruses, SRL + MPA or SRL + Tac was not associated with a different malignancy risk compared with control.<br />Conclusions: Compared with Tac + MPA, SRL regimens were associated with higher risks for patient death and graft loss, although SRL + MPA was associated with a lower risk for posttransplant malignancy in kidney allograft recipients with negative pretransplant HBc, HCV, EBV, or CMV serology.
- Subjects :
- Adult
Allografts
Biomarkers blood
Chi-Square Distribution
Cytomegalovirus Infections blood
Cytomegalovirus Infections diagnosis
Cytomegalovirus Infections mortality
Drug Therapy, Combination
Epstein-Barr Virus Infections blood
Epstein-Barr Virus Infections diagnosis
Epstein-Barr Virus Infections mortality
Female
Graft Survival drug effects
Hepatitis B blood
Hepatitis B diagnosis
Hepatitis B mortality
Hepatitis C blood
Hepatitis C diagnosis
Hepatitis C mortality
Humans
Immunocompromised Host
Immunosuppressive Agents adverse effects
Logistic Models
Male
Middle Aged
Multivariate Analysis
Neoplasms etiology
Odds Ratio
Predictive Value of Tests
Proportional Hazards Models
Registries
Retrospective Studies
Risk Factors
Serologic Tests
Sirolimus adverse effects
Time Factors
Treatment Outcome
United States
Antibodies, Viral blood
Cytomegalovirus Infections immunology
Epstein-Barr Virus Infections immunology
Hepatitis B immunology
Hepatitis C immunology
Immunosuppressive Agents therapeutic use
Kidney Transplantation adverse effects
Kidney Transplantation mortality
Sirolimus therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1534-6080
- Volume :
- 101
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Transplantation
- Publication Type :
- Academic Journal
- Accession number :
- 28121742
- Full Text :
- https://doi.org/10.1097/TP.0000000000001520