Table 2.
De novo KTRs | Switch from tacrolimus | |
---|---|---|
Hard, clinically pertinent outcomes | ||
Death with a functioning graft | No proven benefit vs. tacrolimus | |
Loss of graft function | No proven benefit vs. tacrolimus | |
Rejections | Higher risk with belatacept than with tacrolimus (Mostly T-cell mediated, mostly within a year after initiation) | |
Cardiovascular events | No proven benefit vs. tacrolimus | |
Infectious events | No proven benefit vs. tacrolimus | Higher risk for CMV disease with belatacept |
Cancers | No proven benefit vs. tacrolimus | |
Surrogate endpoints | ||
Estimated GFR | Higher estimated GFR with belatacept than with tacrolimus | |
Donor specific antibodies | Less de novo DSA with belatacept than with tacrolimus | |
Glycemic control | Better glycemic control with belatacept than with tacrolimus |
GFR, glomerular filtration rate; DSA, donor specific antibodies; KTR, kidney transplant recipient.