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. 2024 Sep 27;59(12):1744–1753. doi: 10.1038/s41409-024-02422-z

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — We performed a landmark analysis of cGvHD excluding BOS as risk factor for BOS development. Patients surviving 365 days after allo-HCT were included in the analysis (n = 195). Cumulative incidence of BOS was analyzed by cGvHD onset within the first year after allo-HCT. SHR subdistribution hazard risk, CI confidence interval, cGvHD chronic GvHD, allo-HCT allogeneic hematopoietic cell transplantation.