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Comparison of Reduced-Dose and Labeled-Dose Belatacept Conversion with Immediate or Early Tacrolimus Withdrawal in Kidney Transplant Recipients without Maintenance Corticosteroids

H. Kuzaro1, A. R. Shields2, M. Cuffy2, E. S. Woodle1, K. Pembaur2, S. Safdar2, S. Huang2, G. Krisko2, S. Raabe2, R. Parks2, J. Kremer2

1U Cincinnati, Cincinnati, OH, 2The Christ Hospital, Cincinnati, OH

Meeting: 2020 American Transplant Congress

Abstract number: A-087

Keywords: Co-stimulation, Glomerular filtration rate (GFR), Graft function, Rejection

Session Information

Session Name: Poster Session A: Kidney Immunosuppression: Novel Regimens and Drug Minimization

Session Type: Poster Session

Date: Saturday, May 30, 2020

Session Time: 3:15pm-4:00pm

 Presentation Time: 3:30pm-4:00pm

Location: Virtual

*Purpose: A primary reason for conversion from tacrolimus (TAC) to belatacept (BELA) is to avoid nephrotoxicity. Previous published experiences with BELA-conversion regimens have shown increased rejection risk suggesting a potential need for prolonged TAC taper. The purpose of this study is to compare outcomes of kidney transplant recipients converted from TAC to BELA-based regimens using Reduced-Dose (RDCP) and Labeled-Dose conversion protocols (LDCP) with immediate or early withdrawal of TAC under corticosteroid withdrawal.

*Methods: This retrospective analysis included kidney transplant recipients at a single center converted to BELA-based regimens using a RDCP with immediate TAC withdrawal or 2-4 week tac taper or using a LDCP with immediate TAC withdrawal between Sep 2013-Sep 2019. Both protocols were used with no planned maintenance corticosteroids. The LDCP and RDCP included total initial BELA doses of 65 mg/kg and 50 mg/kg respectively. The primary outcome is mean estimated glomerular filtration rates (eGFRs) at 1-year post-conversion. Secondary outcomes include mean eGFRs at 6 months post-conversion, change in eGFR at 6 and 12 months post-conversion, graft and patient survival, biopsy-proven acute rejection (BPAR), cytomegalovirus (CMV) and BK virus, and leukopenia (defined as white blood cells <2000 cells/mm3) and/or neutropenia (defined as <1500 cell/mm3) within 6 months of conversion.

*Results: 49 patients were converted to BELA-based regimens. There were no differences in induction (~25% of patients per group were considered high immunologic risk). Patients were converted using LDCP (N=22) or RDCP (N=27). Results are in table 1.

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*Conclusions: Renal function is comparable at 6 and 12 months post-conversion with both LDCP and RDCP. Use of LDCP was associated with greater improvement in eGFR at 6 and 12 months compared to those converted with RDCP, which may be due to more DGF in the LDCP group; however, there was more CMV viremia in the LDCP group. Both protocols were associated with increased eGFRs compared to pre-conversion eGFRs. BELA conversion from TAC can be successful with LDCP or RDCP using immediate TAC withdrawal or a 2-4 weeks taper with low BPAR rates (10%) that do not have a negative impact on kidney function nor graft survival (LDCP 90.9% vs. RDCP 92.6%) and excellent patient survival (LDCP 90.9% vs. RDCP 92.6%). Due to a lower CMV rate and trend toward less rejection, the RDCP may be more favorable overall.

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To cite this abstract in AMA style:

Kuzaro H, Shields AR, Cuffy M, Woodle ES, Pembaur K, Safdar S, Huang S, Krisko G, Raabe S, Parks R, Kremer J. Comparison of Reduced-Dose and Labeled-Dose Belatacept Conversion with Immediate or Early Tacrolimus Withdrawal in Kidney Transplant Recipients without Maintenance Corticosteroids [abstract]. Am J Transplant. 2020; 20 (suppl 3). https://atcmeetingabstracts.com/abstract/comparison-of-reduced-dose-and-labeled-dose-belatacept-conversion-with-immediate-or-early-tacrolimus-withdrawal-in-kidney-transplant-recipients-without-maintenance-corticosteroids/. Accessed May 16, 2025.

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