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.
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Data availability
The data analyzed in this study were provided and approved by the Transplant Complications Working Party (TCWP) of the EBMT. The datasets generated and analyzed during the current study are available from the corresponding author on reasonable request after approval of the scientific board of the TCWP of EBMT.
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DP, CP, WB, IM, OP, and ZP contributed to the design of the study, analysis and interpretation of the data. DP wrote the original draft of the manuscript. CP performed statistical analyses. CR, NK, DM, US, RZ, KEG, EF, DB, TL, HLW, CK, HS, and GB contributed to the collection and interpretation of data. All authors reviewed, critically revised, and approved the manuscript.
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DP received honoraria from Novartis and Takeda. NK received honoraria from Sanofi and Neovii. DM received research grants from Novartis, Sanofi and CSL Behring, consulting fees from Novartis, Incyte, Sanofi, Jazz Pharmaceuticals, and Mallinckrodt. RZ received honoraria from Novartis, Incyte, Sanofi, Medac and Mallinckrodt. KEH received travel support and honoraria from Beigene, Sanofi, Johnson&Johnson and Servier. IM received honoraria from Novartis, Sanofi, J&J. OP has received honoraria or travel support from Alexion, Gilead, Jazz, MSD, Neovii, Novartis, Pfizer and Therakos. He has received research support from Incyte and Priothera. He is member of advisory boards to Apogepha, Alexion, Equillium Bio, Jazz, Gilead, Novartis, MSD, Omeros, Orca Bio, Priothera, Sanofi, Shionogi and SOBI. OP acknowledges the support of José Carreras Leukämie-Stiftung (3 R/2019, 23 R/2021), Deutsche Krebshilfe (70113519), Deutsche Forschungsgemeinschaft (PE 1450/7-1, PE 1450/9-1, PE 1450/10-1, PE 1450/11-1) and Stiftung Charité BIH (BIH_PRO_549, Focus Group Vascular Biomedicine). ZP received honoraria from Therakos, Sanofi and Novartis.
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The study was conducted in accordance with the Declaration of Helsinki and was reviewed and approved by the scientific board of the Transplant Complications Working Party of EBMT. As per EBMT data collection policies, written informed consent was obtained from all patients for the use of their data. All methods were conducted in accordance with relevant guidelines and regulations.
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Pulanic, D., Peczynski, C., Boreland, W. et al. Chronic Graft-versus-Host disease trends over 30 years - a study by the EBMT transplant complications working party. Bone Marrow Transplant 60, 1436–1444 (2025). https://doi.org/10.1038/s41409-025-02697-w
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DOI: https://doi.org/10.1038/s41409-025-02697-w


