Modeling graft loss in patients with donor-specific antibody at baseline using the Birmingham-Mayo (BirMay) predictor: Implications for clinical trials.


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
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

2274-2283

Subventions

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.

Auteurs

Andrew Bentall (A)

Department of Renal Medicine, Queen Elizabeth Hospital Birmingham, Birmingham, UK.
William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

Byron H Smith (BH)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

Manuel Moreno Gonzales (MM)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.
Servicio de Cirugía General, Americana, Lima, Perú.

Keisha Bonner (K)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

Walter D Park (WD)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

Lynn D Cornell (LD)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.

Patrick G Dean (PG)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

Carrie A Schinstock (CA)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

Richard Borrows (R)

Department of Renal Medicine, Queen Elizabeth Hospital Birmingham, Birmingham, UK.

Carmen Lefaucheur (C)

Department of Nephrology and Kidney Transplantation, Saint-Louis Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.

Alexandre Loupy (A)

Department of Nephrology-Transplantation Necker Hospital, Assistance Publique-Hôpitaux de Paris, University Paris Descartes, Paris, France.
Paris Cardiovascular Research Centre - Biostatistics Unit University Paris Descartes, UMR-S970, Paris, France.

Mark D Stegall (MD)

William J. von Liebig Transplant Center, Mayo Clinic, Rochester, Minnesota.

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Classifications MeSH