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An automated histological classification system for precision diagnostics of kidney allografts

  • Daniel Yoo
  • , Valentin Goutaudier
  • , Gillian Divard
  • , Juliette Gueguen
  • , Brad C. Astor
  • , Olivier Aubert
  • , Marc Raynaud
  • , Zeynep Demir
  • , Julien Hogan
  • , Patricia Weng
  • , Jodi Smith
  • , Rouba Garro
  • , Bradley A. Warady
  • , Rima S. Zahr
  • , Marta Sablik
  • , Katherine Twombley
  • , Lionel Couzi
  • , Thierry Berney
  • , Olivia Boyer
  • , Jean Paul Duong-Van-Huyen
  • Magali Giral, Alaa Alsadi, Pierre A. Gourraud, Emmanuel Morelon, Moglie Le Quintrec, Sophie Brouard, Christophe Legendre, Dany Anglicheau, Jean Villard, Weixiong Zhong, Nassim Kamar, Oriol Bestard, Arjang Djamali, Klemens Budde, Mark Haas, Carmen Lefaucheur, Marion Rabant, Alexandre Loupy
  • PARCC - Paris-Centre de Recherche Cardiovasculaire
  • Université Paris Cité
  • Centre Hospitalier Régional Universitaire de Tours
  • University of Wisconsin-Madison
  • Hôpital Robert Debré
  • University of California at Los Angeles
  • University of Washington
  • Emory University
  • University of Missouri at Kansas City
  • University of Tennessee Health Science Center
  • Medical University of South Carolina
  • Centre Hospitalier Universitaire de Bordeaux
  • University of Geneva
  • CHU de Nantes
  • Hôpital Édouard Herriot
  • CHU Montpellier
  • CHU de Toulouse
  • Hospital Vall d'Hebron
  • Maine Medical Center
  • harité – Universitätsmedizin Berlin
  • Cedars-Sinai Medical Center

Producción científicarevisión exhaustiva

56 Citas (Scopus)

Resumen

For three decades, the international Banff classification has been the gold standard for kidney allograft rejection diagnosis, but this system has become complex over time with the integration of multimodal data and rules, leading to misclassifications that can have deleterious therapeutic consequences for patients. To improve diagnosis, we developed a decision-support system, based on an algorithm covering all classification rules and diagnostic scenarios, that automatically assigns kidney allograft diagnoses. We then tested its ability to reclassify rejection diagnoses for adult and pediatric kidney transplant recipients in three international multicentric cohorts and two large prospective clinical trials, including 4,409 biopsies from 3,054 patients (62.05% male and 37.95% female) followed in 20 transplant referral centers in Europe and North America. In the adult kidney transplant population, the Banff Automation System reclassified 83 out of 279 (29.75%) antibody-mediated rejection cases and 57 out of 105 (54.29%) T cell-mediated rejection cases, whereas 237 out of 3,239 (7.32%) biopsies diagnosed as non-rejection by pathologists were reclassified as rejection. In the pediatric population, the reclassification rates were 8 out of 26 (30.77%) for antibody-mediated rejection and 12 out of 39 (30.77%) for T cell-mediated rejection. Finally, we found that reclassification of the initial diagnoses by the Banff Automation System was associated with an improved risk stratification of long-term allograft outcomes. This study demonstrates the potential of an automated histological classification to improve transplant patient care by correcting diagnostic errors and standardizing allograft rejection diagnoses. ClinicalTrials.gov registration: NCT05306795 .

Idioma originalEnglish
Páginas (desde-hasta)1211-1220
Número de páginas10
PublicaciónNature Medicine
Volumen29
N.º5
DOI
EstadoPublished - may 2023
Publicado de forma externa

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