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. 2024 Aug 12;14(1):134. doi: 10.1038/s41408-024-01109-4

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 1 — A Heterogeneity by t(11:14) and BCL2 expression status in the BELLINI trial [18]. Heterogeneity in PFS and OS outcomes were seen between patients with t(11;14) or high BCL2 expression and those with no t(11;14) or low BCL2 expression. B Heterogeneity by age in the OCEAN trial [17]. Heterogeneity by age was observed for both PFS (p = 0.033^het) and OS (p = 0.006^het). Dex dexamethasone, mel melflufen, pom pomalidomide, pts patients, Vd bortezomib and dexamethasone, VenVd venetoclax, bortezomib, and dexamethasone.