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. 2019 Mar 7;9(3):32. doi: 10.1038/s41408-019-0191-y

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© The Author(s) 2019

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — a Proportion of patients receiving proteasome inhibitor + immunomodulatory drug based, proteasome inhibitor based, immunomodulator based, and other induction therapies in patients with (i) de novo del(17p), (ii) high-risk translocation and (iii) standard-risk FISH. b Best response to induction therapy in patients with de novo del(17p), high-risk translocation and standard-risk FISH, expressed as percentage within each category. The numbers in parentheses indicate the absolute number of patients. CR complete response, MR minimal response, PR partial response, PD progressive disease, sCR stringent CR, VGPR very good partial response, and SD Stable disease