TY - JOUR
T1 - Primary pediatric deceased-donor kidney transplant recipients outcomes by immunosuppression induction received in the United States
AU - Riad, Samy
AU - Jackson, Scott
AU - Chinnakotla, Srinath
AU - Verghese, Priya
N1 - Funding Information:
We want to acknowledge both the University of Minnesota department of medicine for providing the funds to acquire the SRTR standard analysis file and the Fairview Health Services for providing the statistical support needed for this project. Special thanks to Stephanie Taylor, a project specialist at the division of surgery, for her editorial support.
Publisher Copyright:
© 2020 Wiley Periodicals LLC
PY - 2021/8
Y1 - 2021/8
N2 - Background: We studied the association of induction immunosuppression and pediatric deceased-donor kidney recipient and graft survival. Methods: We utilized the SRTR to evaluate all primary pediatric deceased-donor kidney transplants from January 1st, 2000, through December 2018. We included only recipients who were maintained on tacrolimus and mycophenolate. Recipients were grouped by induction type: alemtuzumab n = 320, r-ATG n = 2091 and IL-2RA n = 2165. Recipient and allograft survival, and their predictors, were examined. Models were adjusted for age, sex, ethnicity, HLA-antigen mismatches, transplant year, steroid maintenance, pre-emptive transplantation and payor type, with the transplant center included as a random effect. Results: Rejection rates at 6 months (alemtuzumab 8.6% vs r-ATG 7.8% vs IL2-RA 9.2%; P =.30) and 12 months (alemtuzumab 17.2% vs r-ATG 15.7% vs IL2-RA 16.5%; P =.70) were not significantly different between induction groups. In the multivariable models, compared to IL-2RA neither alemtuzumab nor r-ATG was associated with improved recipient [alemtuzumab (HR 1.06, P =.88); r-ATG (HR 1.03, P =.84)] or graft survival [alemtuzumab (HR 1.18, P =.32); r-ATG (HR 1.10, P =.21)]. Conclusion: In this large cohort of standard immunological risk primary pediatric deceased-donor kidney recipients on tacrolimus and mycophenolate maintenance, depletional induction regimens were not associated with better rejection rates, recipient, or graft survival compared to IL-2RA induction. Racial, payor type, and sex-related outcome disparities were significant in this group independent of the induction choice.
AB - Background: We studied the association of induction immunosuppression and pediatric deceased-donor kidney recipient and graft survival. Methods: We utilized the SRTR to evaluate all primary pediatric deceased-donor kidney transplants from January 1st, 2000, through December 2018. We included only recipients who were maintained on tacrolimus and mycophenolate. Recipients were grouped by induction type: alemtuzumab n = 320, r-ATG n = 2091 and IL-2RA n = 2165. Recipient and allograft survival, and their predictors, were examined. Models were adjusted for age, sex, ethnicity, HLA-antigen mismatches, transplant year, steroid maintenance, pre-emptive transplantation and payor type, with the transplant center included as a random effect. Results: Rejection rates at 6 months (alemtuzumab 8.6% vs r-ATG 7.8% vs IL2-RA 9.2%; P =.30) and 12 months (alemtuzumab 17.2% vs r-ATG 15.7% vs IL2-RA 16.5%; P =.70) were not significantly different between induction groups. In the multivariable models, compared to IL-2RA neither alemtuzumab nor r-ATG was associated with improved recipient [alemtuzumab (HR 1.06, P =.88); r-ATG (HR 1.03, P =.84)] or graft survival [alemtuzumab (HR 1.18, P =.32); r-ATG (HR 1.10, P =.21)]. Conclusion: In this large cohort of standard immunological risk primary pediatric deceased-donor kidney recipients on tacrolimus and mycophenolate maintenance, depletional induction regimens were not associated with better rejection rates, recipient, or graft survival compared to IL-2RA induction. Racial, payor type, and sex-related outcome disparities were significant in this group independent of the induction choice.
KW - deceased donor
KW - induction
KW - kidney transplant
KW - pediatric
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U2 - 10.1111/petr.13928
DO - 10.1111/petr.13928
M3 - Article
C2 - 33314638
AN - SCOPUS:85097391001
SN - 1397-3142
VL - 25
JO - Pediatric Transplantation
JF - Pediatric Transplantation
IS - 5
M1 - e13928
ER -