Modeling graft loss in patients with donor-specific antibody at baseline using the Birmingham-Mayo (BirMay) predictor: Implications for clinical trials.
Allografts
Cohort Studies
Female
Glomerular Filtration Rate
Graft Rejection
/ diagnosis
Graft Survival
/ immunology
HLA Antigens
/ immunology
Histocompatibility
Humans
Incidence
Isoantibodies
/ immunology
Kidney Failure, Chronic
/ immunology
Kidney Function Tests
Kidney Transplantation
/ mortality
Male
Middle Aged
Models, Statistical
Prognosis
Risk Assessment
/ methods
Risk Factors
Survival Rate
Tissue Donors
/ supply & distribution
United States
/ epidemiology
alloantibody
clinical research/practice
kidney (allograft) function/dysfunction
kidney transplantation/nephrology
pathology/histopathology
protocol biopsy
risk assessment/risk stratification
Journal
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
28
09
2018
revised:
31
12
2018
accepted:
06
02
2019
pubmed:
16
2
2019
medline:
1
9
2020
entrez:
16
2
2019
Statut:
ppublish
Résumé
Predicting which renal allografts will fail and the likely cause of failure is important in clinical trial design to either enrich patient populations to be or as surrogate efficacy endpoints for trials aimed at improving long-term graft survival. This study tests our previous Birmingham-Mayo model (termed the BirMay Predictor) developed in a low-risk kidney transplant population in order to predict the outcome of patients with donor specific alloantibody (DSA) at the time of transplantation and identify new factors to improve graft loss prediction in DSA+ patients. We wanted define ways to enrich the population for future therapeutic intervention trials. The discovery set included 147 patients from Mayo Cohort and the validation set included 111 patients from the Paris Cohort-all of whom had DSA at the time of transplantation. The BirMay predictor performed well predicting 5-year outcome well in DSA+ patients (Mayo C statistic = 0.784 and Paris C statistic = 0.860). Developing a new model did not improve on this performance. A high negative predictive value of greater than 90% in both cohorts excluded allografts not destined to fail within 5 years. We conclude that graft-survival models including histology predict graft loss well, both in DSA+ cohorts as well as DSA- patients.
Identifiants
pubmed: 30768833
doi: 10.1111/ajt.15312
pii: S1600-6135(22)09193-6
doi:
Substances chimiques
HLA Antigens
0
Isoantibodies
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
2274-2283Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK088791
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002379
Pays : United States
Informations de copyright
© 2019 The American Society of Transplantation and the American Society of Transplant Surgeons.