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Toxicity Driven Conversion to Belatacept in Kidney Transplant Recipients

E. Cohen, W. Asch, R. Formica, E. Tichy.

Yale-New Haven Transplantation Center, New Haven, CT.

Meeting: 2015 American Transplant Congress

Abstract number: C72

Keywords: Immunosuppression, Kidney transplantation

Session Information

Session Name: Poster Session C: Immunosuppression/Compliance

Session Type: Poster Session

Date: Monday, May 4, 2015

Session Time: 5:30pm-6:30pm

 Presentation Time: 5:30pm-6:30pm

Location: Exhibit Hall E

Purpose: Evaluate the result of conversion to belatacept from calcineurin inhibitor (CNI) or TOR inhibitor based regimens due to toxicities in kidney transplant recipients (KTR).

Methods: A retrospective chart review was conducted of adult KTR at our center who were converted to belatacept from either a CNI or TOR inhibitor. Data was collected at baseline, 1 month, 3 months and 6 months post-conversion. Primary outcome was indication for changing immunosuppression. Secondary outcomes include change in toxicity, change in renal function using serum creatinine (SCr) and calculated creatinine clearance (CrCl), rates of failed conversion, biopsy proven acute rejection (BPAR) and infection. Student's t-test was used to compare renal function changes.

Results: Twenty three patients were included in this analysis. Fourteen patients were converted from a CNI regimen and nine patients were converted from an mTOR. For patients converted from CNIs, twelve (85.7%) were converted for neurotoxicities and two (14.3%) for other indications. For patients converted from TORs, indications include hyperlipidemia (33.4%), edema (22.2%), pneumonitis (22.2%), and wound healing (22.2%). Of these, 17 patients (73.9%) had improvement in their indication after converting to belatacept. Three patients (13%) did not have improvement and in three patients (13%) failed conversion to belatacept due to infusion related adverse effects. Other adverse events include one urinary tract infection (UTI), one resistant CMV viremia, and one case of BPAR requiring treatment.

Conclusion: The majority of toxicities resolved upon conversion to belatacept. In the conversion from CNIs there was an additional benefit of improved renal function.

Table 1
  Number Percentage
N 23  
Improvement 17 73.9%
No improvement 3 13%
Failed conversion 3 13%
CNI: Indication for conversion (n=14)
Neurotoxicity 12 85.7%
CNI kidney injury 1 7.2%
Weight gain 1 7.2%
TOR: Indication for conversion (n=9)
Edema 2 22.2%
Pneumonitis 2 22.2%
Hyperlipidemia 3 33.4%
Wound healing 2 22.2%
Adverse Effects
Infusion reaction 3 13%
Infection 2 8.7%
BPAR 1 4.3%
Table 2: Kidney Function
All Patients (N=23)
    p-value
Baseline SCr 1.7±0.9  
SCr at 6 months 1.4±0.5 0.0106
Baseline CrCl 45.9±22.3  
CrCl at 6 months 49.5±16.9 0.195
Conversion from CNI (n=14)
Baseline SCr 1.9±0.9  
SCr at 6 months 1.3±0.6 0.005
Baseline CrCl 37.8±19.9  
CrCl at 6 months 48.1±19.1 0.0072
Conversion from TOR (n=9)
Baseline SCr 1.5±0.8  
SCr at 6 months 1.4±0.5 0.645
Baseline CrCl 55.8±22.4  
CrCl at 6 months 51.3±14.5 0.279
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To cite this abstract in AMA style:

Cohen E, Asch W, Formica R, Tichy E. Toxicity Driven Conversion to Belatacept in Kidney Transplant Recipients [abstract]. Am J Transplant. 2015; 15 (suppl 3). https://atcmeetingabstracts.com/abstract/toxicity-driven-conversion-to-belatacept-in-kidney-transplant-recipients/. Accessed May 11, 2025.

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