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Belatacept Versus Tacrolimus for Kidney Transplant Recipients of Deceased Donors With Acute Kidney Injury: US
Junji Yamauchi1,2,3, Divya Raghavan1, Duha Jweehan1
1Division of Nephrology and Hypertension, Department of Internal Medicine, Spencer Fox Eccles School of Medicine at the University of Utah, Salt Lake City, UT.
Background:
It is unclear whether kidney grafts from deceased donors with acute kidney injury (AKI) are more vulnerable to calcineurin inhibitor nephrotoxicity, and whether de novo use of belatacept is more beneficial than tacrolimus for recipients of these types of kidney transplants.
Methods:
In this retrospective cohort study using the US Organ Procurement and Transplantation Network database, we created 1:4 matches with highly similar characteristics for recipients of AKI-donor kidneys receiving belatacept versus tacrolimus for initial maintenance immunosuppression and compared outcomes for graft function, patient and graft survival, and rejection.
Results:
The matched cohort consisted of 567 and 2268 recipients administered belatacept and tacrolimus, respectively. Posttransplant estimated glomerular filtration rate was significantly higher in the belatacept group at 6 mo (58.2 ± 24.2 versus 54.6 ± 21.6 mL/min/1.73 m 2 , P < 0.001); however, the between-group difference did not reach statistical significance at 12 mo (57.2 ± 24.3 versus 55.7 ± 22.2 mL/min/1.73 m 2 , P = 0.057). Median follow-up periods were 3.2 and 3.1 y for patient and graft survival, respectively. There were no significant differences between belatacept versus tacrolimus for mortality (hazard ratio 1.18 [95% confidence interval, 0.95-1.47], P = 0.14) or death-censored graft failure (hazard ratio 1.17 [0.85-1.61], P = 0.33). Rejection rate within 12 mo was significantly higher in the belatacept group (13% versus 7%, P < 0.001).
Conclusions:
In this matched cohort study, initial use of belatacept for AKI-donor kidney recipients was associated with small benefits in early graft function when compared with tacrolimus. Although rejection risk was significantly higher in recipients administered belatacept, patient and graft survival were not significantly different between groups.
Insights
Belatacept showed slightly better early kidney graft function than tacrolimus in acute kidney injury (AKI) donor transplants. However, belatacept increased rejection risk without impacting long-term patient or graft survival.
Area of Science:
- Nephrology
- Transplantation Immunology
- Immunosuppression
Background:
- Assessing the vulnerability of kidney grafts from deceased donors with acute kidney injury (AKI) to calcineurin inhibitor nephrotoxicity.
- Evaluating the comparative efficacy of de novo belatacept versus tacrolimus in kidney transplant recipients receiving AKI donor grafts.
Purpose of the Study:
- To compare the outcomes of belatacept versus tacrolimus in kidney transplant recipients using grafts from deceased donors with AKI.
- To investigate differences in graft function, patient and graft survival, and rejection rates between the two immunosuppressive strategies.
Main Methods:
- Retrospective cohort study utilizing the US Organ Procurement and Transplantation Network database.
- 1:4 matching of recipients of AKI-donor kidneys based on highly similar characteristics.
- Comparison of outcomes including estimated glomerular filtration rate (eGFR), patient and graft survival, and rejection rates between belatacept and tacrolimus groups.
Main Results:
- Belatacept group showed significantly higher eGFR at 6 months post-transplant (58.2 vs 54.6 mL/min/1.73 m²).
- No significant differences in patient mortality (HR 1.18) or death-censored graft failure (HR 1.17) between groups.
- Higher rejection rate within 12 months in the belatacept group (13% vs 7%).
Conclusions:
- Initial belatacept use in AKI-donor kidney recipients offers minor early graft function benefits compared to tacrolimus.
- Belatacept is associated with a significantly increased risk of rejection within the first year.
- Despite higher rejection rates, belatacept did not significantly impact overall patient or graft survival in this cohort.
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