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Belatacept Conversion in Adult Kidney Transplant Recipients for Cause: A Single Center Observational Cohort.

M. Savic,1 M. Cruz,2 A. Rossi,1 J. Vella.1

1Maine Transplant Program, Maine Medical Center, Portland, ME
2University of Connecticut, Storrs, CT.

Meeting: 2016 American Transplant Congress

Abstract number: D146

Keywords: Co-stimulation, Efficacy, Immunosuppression, Kidney transplantation

Session Information

Session Name: Poster Session D: Kidney Immunosuppression: Novel Agents

Session Type: Poster Session

Date: Tuesday, June 14, 2016

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Halls C&D

Background: Calcineurin inhibition (CNI) is the single most effective strategy to prevent allograft rejection however tolerability is limited by toxicity. To date, alternate strategies have been limited by serious adverse reactions including reduced patient & graft survival. Belatacept, a novel costimulatory blockade agent approved for de novo rejection prophylaxis, offers a potential alternate conversion strategy for patients with serious CNI toxicity.

Methods: A retrospective cohort study of adult KT recipients who transitioned from CNI to belatacept between March 2012 and August 2015 was performed. Data on allograft function was collected at baseline, 3 months and 6 months. Primary outcome was the number of patients that remained on belatacept therapy. Secondary outcomes include change in allograft function using serum creatinine (Scr), calculated creatinine clearance (CrCl), graft failures, death, and tolerance.

Results: Twenty-three kidney transplant recipientstransitioned from CNI to belatacept were identified. All patients were Caucasian, mean age was 53 years and 55% were female. Indication for belatacept conversion included the following: advanced chronic allograft nephropathy (CAN) 35 %, acute nephrotoxicity 35%, non-adherence 22%, and neurotoxicity 8% of patients. Of the 8 patients with CAN, 50% lost their graft, including one death with functioning graft and only 50% remained on therapy. Of the 15 patients converted to belatacept for all other indications, 93% remained on belatacept therapy. In addition 14/15 patients in the non-CAN group had a statistically significant increase in creatinine clearance at 6 months with average increase of 9ml/min/1.73m2 (95% CI 1.8 to 16 ml/min/1.73m2, p=0.018). In terms of safety, no infusion related adverse effects were noted and one patient reported cough. The only death was not related to belatacept administration.

 Indication for Conversion  N=  Days to Conversion  Graft Failure  Death  Ongoing Belatacept
 Acute Nephrotoxicity  8  524  0  0  8
 Adherence  5  219  1  0  4
 Neurotoxicity  2  98  0  0  2
 Subtotal  15    1  0  14
 CAN  8  2355  4  1  4

Conclusions: Conversion to belatacept from CNI is well tolerated and resulted in improvement of allograft function in most patients without CAN. Based on our experience, patients with CAN are unlikely to see benefit from conversion to belatacept.

CITATION INFORMATION: Savic M, Cruz M, Rossi A, Vella J. Belatacept Conversion in Adult Kidney Transplant Recipients for Cause: A Single Center Observational Cohort. Am J Transplant. 2016;16 (suppl 3).

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To cite this abstract in AMA style:

Savic M, Cruz M, Rossi A, Vella J. Belatacept Conversion in Adult Kidney Transplant Recipients for Cause: A Single Center Observational Cohort. [abstract]. Am J Transplant. 2016; 16 (suppl 3). https://atcmeetingabstracts.com/abstract/belatacept-conversion-in-adult-kidney-transplant-recipients-for-cause-a-single-center-observational-cohort/. Accessed May 9, 2025.

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