Key result
Belatacept improved renal function at 12 months (MD 11.7) and reduced new onset diabetes (OR 0.43) compared to calcineurin inhibitors, with no difference in acute rejection.
Why the study?
Does belatacept improve outcomes compared to calcineurin inhibitors in adult kidney transplant recipients?
Systematic Review
Does belatacept improve outcomes compared to calcineurin inhibitors in adult kidney transplant recipients?
Mean Difference: 11.7
Belatacept may offer better renal function and metabolic profiles than CNIs in kidney transplant recipients without increasing acute rejection, though PTLD risk exists in EBV-seronegative patients.
No difference in acute rejection with belatacept versus CNIs; supports CNI-sparing regimens while leaving long-term outcomes open for further RCTs.
BACKGROUND: Belatacept was intended to provide better outcomes for kidney transplant (KT) recipients by allowing minimization/withdrawal of calcineurin inhibitors (CNI) and steroids. METHODS: We searched for randomized controlled trials (RCTs) in adult KT comparing belatacept with CNIs. Methodological quality was assessed. Meta-analyses were performed to calculate odds ratios (OR) and mean differences (MD). RESULTS: Six RCTs were included. Pooled analyses found no differences for acute rejection at any time point. Renal function [Calculated glomerular filtration rate (cGFR)] was better with belatacept at 12 and 24 months (MD = 11.7 and 13.7 ml/min/1.73 m(2) ). New onset diabetes after transplantation was lower with belatacept at 12 months (OR = 0.43). Systolic and diastolic blood pressures were lower at 12 months (MD -7.2 and -3.1 mmHg) as were triglycerides at 12 and 24 months (MD = -32.9 and -41.7 mg/dl). Total and low-density lipoprotein cholesterol were lower with belatacept at 24 months (MD = -19.8 and -10.6 mg/dl). There were no differences for other outcomes. CONCLUSION: Limited available data suggest a potential benefit for belatacept by reducing the risk of CNI toxicity, especially renal function, without evidence of increased acute rejection. There were no safety issues apart from a possible risk of post-transplant lymphoproliferative disorder in Epstein-barr virus-seronegative recipients. Further studies are required to confirm this benefit.
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Talawila et al. (2015) conducted a systematic review in Kidney transplant. Belatacept vs. Calcineurin inhibitors (CNIs) was evaluated on Renal function (cGFR) at 12 months (MD 11.7). Belatacept improved renal function at 12 months (MD 11.7) and reduced new onset diabetes (OR 0.43) compared to calcineurin inhibitors, with no difference in acute rejection.
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