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Renal Function Outcomes by HLA Mismatch in De Novo Kidney Transplant Recipients Receiving Everolimus PlusReduced-Dose Cyclosporine versus Mycophenolate Plus Standard-Dose Cyclosporine: 24-Month Subanalysis of A1202 Study.

K. Yoshida,1 Y. Watarai,2 K. Nakagawa,3 O. Kamisawa.4

1Kitasato University, Sagamihara, Japan
2Nagoya Daini Red Cross Hospital, Nagoya, Japan
3Ichikawa General Hospital, Tokyo Dental College, Ichikawa, Japan
4Novartis Pharma K.K., Tokyo, Japan

Meeting: 2017 American Transplant Congress

Abstract number: D81

Keywords: HLA matching, Kidney transplantation, Proteinuria, Renal function

Session Information

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

Session Type: Poster Session

Date: Tuesday, May 2, 2017

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

 Presentation Time: 6:00pm-7:00pm

Location: Hall D1

Purpose: High levels of human leukocyte antigen (HLA) mismatches are a key determinant of kidney allograft survival. Here, we present 24-month (M) subanalysis of the A1202 study wherein influence of HLA mismatch on renal function outcomes was compared in kidney transplant recipients (KTxRs) receiving everolimus (EVR) plus reduced-dose cyclosporine (rCsA) vs mycophenolate mofetil (MMF) plus standard-dose CsA (sCsA).

Methods: A1202 was a 12M core plus 12M extension follow-up, multicenter, open-label study comparing efficacy and safety of 1.5 mg/day EVR plus rCsA (EVR+rCsA) vs 2 g/day MMF plus sCsA (MMF+sCsA) in Japanese de novo KxTRs. Patients completing the core and extension follow-up were included in this subanaylsis (n=50 each arm). Renal function [eGFR by MDRD, serum creatinine, and creatinine clearance] and composite efficacy failure events [treated biopsy-proven acute rejection, graft loss, death, or loss to follow-up] were determined at M24 in HLA mismatch groups (<3 vs ≥3).

Results: KTxRs were categorized by treatment and level of mismatch into 4 groups (Table). Although treatment differences were not statistically significant, mean eGFR remained numerically higher in EVR+rCsA vs MMF+sCsA arm for both mismatch groups up to M24 (<3: 60.1 vs 56.8 mL/min/1.73m2, P=0.51; ≥3: 62.1 vs 56.4 mL/min/1.73m2; P=0.24). Serum creatinine levels and creatinine clearance were similar in both arms for both mismatch groups. More KTxRs in EVR+rCsA vs MMF+sCsA arm (18.8% vs 8.1%) had sub-nephrotic proteinuria for mismatch group ≥3, whereas more KTxRs in MMF+sCsA arm had sub-nephrotic proteinuria for mismatch group <3. Composite efficacy failure events were comparable in both arms for both mismatch groups. No new safety signals were noted.

Conclusion: These results suggest that renal function outcomes are similar up to 24 months in KTxRs receiving EVR+rCsA vs MMF+sCsA regardless of HLA mismatch level.

CITATION INFORMATION: Yoshida K, Watarai Y, Nakagawa K, Kamisawa O. Renal Function Outcomes by HLA Mismatch in De Novo Kidney Transplant Recipients Receiving Everolimus PlusReduced-Dose Cyclosporine versus Mycophenolate Plus Standard-Dose Cyclosporine: 24-Month Subanalysis of A1202 Study. Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Yoshida K, Watarai Y, Nakagawa K, Kamisawa O. Renal Function Outcomes by HLA Mismatch in De Novo Kidney Transplant Recipients Receiving Everolimus PlusReduced-Dose Cyclosporine versus Mycophenolate Plus Standard-Dose Cyclosporine: 24-Month Subanalysis of A1202 Study. [abstract]. Am J Transplant. 2017; 17 (suppl 3). https://atcmeetingabstracts.com/abstract/renal-function-outcomes-by-hla-mismatch-in-de-novo-kidney-transplant-recipients-receiving-everolimus-plusreduced-dose-cyclosporine-versus-mycophenolate-plus-standard-dose-cyclosporine-24-month-subana/. Accessed May 13, 2025.

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