Rethinking the advantage of zero-HLA mismatches in unrelated living donor kidney transplantation: implications on kidney paired donation

被引:13
作者
Casey, Michael Jin [1 ]
Wen, Xuerong [1 ]
Rehman, Shehzad [1 ]
Santos, Alfonso H. [1 ]
Andreoni, Kenneth A. [2 ]
机构
[1] Univ Florida, Dept Med, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Surg, Gainesville, FL 32610 USA
关键词
human leukocyte antigen; kidney; living donor; mismatch; paired donation; transplant; LIVE-DONOR; RENAL-TRANSPLANTATION; GRAFT FAILURE; RECIPIENTS; SURVIVAL; IMMUNOSUPPRESSION; ALLOCATION; PROGRAMS; OUTCOMES; IMPACT;
D O I
10.1111/tri.12495
中图分类号
R61 [外科手术学];
学科分类号
摘要
The OPTN/UNOS Kidney Paired Donation (KPD) Pilot Program allocates priority to zero-HLA mismatches. However, in unrelated living donor kidney transplants (LDKT)the same donor source in KPDno study has shown whether zero-HLA mismatches provide any advantage over >0 HLA mismatches. We hypothesize that zero-HLA mismatches among unrelated LDKT do not benefit graft survival. This retrospective SRTR database study analyzed LDKT recipients from 1987 to 2012. Among unrelated LDKT, subjects with zero-HLA mismatches were compared to a 1:1-5 matched (by donor age +/- 1year and year of transplantation) control cohort with >0 HLA mismatches. The primary endpoint was death-censored graft survival. Among 32,654 unrelated LDKT recipients, 83 had zero-HLA mismatches and were matched to 407 controls with >0 HLA mismatches. Kaplan-Meier analyses for death-censored graft and patient survival showed no difference between study and control cohorts. In multivariate marginal Cox models, zero-HLA mismatches saw no benefit with death-censored graft survival (HR=1.46, 95% CI 0.78-2.73) or patient survival (HR=1.43, 95% CI 0.68-3.01). Our data suggest that in unrelated LDKT, zero-HLA mismatches may not offer any survival advantage. Therefore, particular study of zero-HLA mismatching is needed to validate its place in the OPTN/UNOS KPD Pilot Program allocation algorithm.
引用
收藏
页码:401 / 409
页数:9
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