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. 2021 Dec 18;14:295. doi: 10.1186/s12920-021-01140-5

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© The Author(s) 2021

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — Kaplan–Meier (KM) survival analysis of genomic subgroups versus MDMS8. KM survival analysis showing overall survival (OS) of patients carrying one or more of the following genomic aberrations: [t(4;14), t(14;16), gain1q or del17p] versus the remaining patients (left); overall survival (OS) of patients with genomic aberrations [t(4;14), t(14;16), gain1q or del17p] in MDMS8 versus the same subset of patients in non-MDMS8 subgroups (middle); and progression free survival (PFS) of patients with genomic aberrations [(t(4;14), t(14;16), gain1q or del17p] in MDMS8 versus the same subset of patients in non-MDMS8 subgroups