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. 2022 Jul 16;195(1):65–74. doi: 10.1007/s10549-022-06643-y

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© The Author(s) 2022

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 — A Pharmacokinetic profile of endoxifen steady-state concentrations (n = 301) stratified based on CYP2D6 phenotype, median (IQR). PM poor metabolizer 7.6 (6.6–9.0); IM, intermediate metabolizer 21.5 (13.9–30.2); NM, normal metabolizer 31.5 (22.9–40.3). B Pharmacokinetic profile of endoxifen steady-state concentrations (n = 301) stratified on CYP2D6 activity score (AS) based on their allele combination, median (IQR). PM/PM 7.6 (6.6–9.0), IM/PM 11.2 (9.1–12.4), IM/IM 15.2 (13.3–24.1), NM/PM 26.6 (19.0–32.8), NM/IM 26.6 (19.2–32.8), NM/NM 34.1 (25.6–44.3)