Chronic Graft-versus-Host disease trends over 30 years - a study by the EBMT transplant complications working party

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Drazen Pulanic - , University of Zagreb (Autor:in)
  • Christophe Peczynski - , Sorbonne Université (Autor:in)
  • William Boreland - , Sorbonne Université (Autor:in)
  • Christina Rautenberg - , Universitätsklinikum Essen (Autor:in)
  • Nicolaus Kröger - , Universität Hamburg (Autor:in)
  • David Michonneau - , Hôpital Saint-Louis AP-HP (Autor:in)
  • Urpu Salmenniemi - , University of Helsinki (Autor:in)
  • Robert Zeiser - , Albert-Ludwigs-Universität Freiburg (Autor:in)
  • Katharina Egger-Heidrich - , Medizinische Klinik und Poliklinik I, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Edouard Forcade - , Haut-Lévêque Hospital (Autor:in)
  • Didier Blaise - , Aix-Marseille Université (Autor:in)
  • Thomas Luft - , Universität Heidelberg (Autor:in)
  • Hélène Labussière-Wallet - , Hospices civils de Lyon (Autor:in)
  • Ivan Moiseev - , Pavlov First State Medical University of St. Petersburg (Autor:in)
  • Christian Koenecke - , Medizinische Hochschule Hannover (MHH) (Autor:in)
  • Helene Schoemans - , KU Leuven (Autor:in)
  • Grzegorz Basak - , Medical University of Warsaw (Autor:in)
  • Olaf Penack - , Charité – Universitätsmedizin Berlin (Autor:in)
  • Zinaida Peric - , University Hospital Centre Zagreb, University of Rijeka (Autor:in)

Abstract

We assessed whether the incidence and outcomes of chronic Graft-versus-Host Disease (cGvHD) after allogeneic hematopoietic stem cell transplantation (alloHSCT) have changed over 30 years. We studied 102,275 adults with hematological malignancies receiving a first alloHSCT from identical siblings or unrelated donors. We compared 3 decades: (I) 1990–1999 vs. (II) 2000–2009 vs. (III) 2010–2019. Over time, patients were older at transplantation, received more PBSC, unrelated donor transplants, reduced intensity conditioning, in vivo T-cell depletion and an ATG prophylaxis, and less TBI. cGvHD incidence at 48 months was 37.3% [36.2–38.4] in I decade vs. 44.9% [44.3–45.5] in II decade vs. 39.1% [38.7–39.5] in III decade, and incidence of extensive cGvHD at 48 months was 18.1% [17.3–19] vs. 22.2% [21.7–22.6] vs. 19.2% [18.9–19.5] over decades. In multivariate analysis, more cGvHD developed in II than in I decade (HR 1.14, 95% CI 1.09–1.21), but no difference was found between III and I decade (HR 1.01, 95% CI 0.96–1.06). Among patients with cGvHD, NRM at 48 months decreased over decades (21.3% [19.8–22.8] vs. 21% [20.3–21.7] vs. 19.7% [19.1–20.2], p < 0.001). Our data show unchanged cGvHD incidences over time and a high NRM in patients after cGvHD diagnosis.

Details

OriginalspracheEnglisch
Seiten (von - bis)1436-1444
Seitenumfang9
FachzeitschriftBone marrow transplantation
Jahrgang60
Ausgabenummer11
PublikationsstatusVeröffentlicht - Nov. 2025
Peer-Review-StatusJa

Externe IDs

PubMed 40830236

Schlagworte