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. 2021 Jun 15;28(13):9086–9095. doi: 10.1245/s10434-021-10187-8

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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/.

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Fig. 2. — Adverse event (AE) overview in the mITT group. a Proportional distribution (%) of AEs classified according to National Cancer Institute CTCAE v.4.0, categorized as EAEs (bottom column) or UAEs (top column) [please see the Methods section (Assessment of Endpoints) for respective details]. b Proportional distribution (%) of patients experiencing (n) cumulative UAEs (left)/EAEs (right) over 30 days post-interventional follow-up. mITT modified intention-to-treat group, UAEs unexpected adverse events, EAEs expected adverse events, CTCAE Common Terminology Criteria for Adverse Events, AE adverse event