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. 2020 May 7;10:47. doi: 10.1186/s13550-020-00638-w

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© The Author(s) 2020

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. 3 — Box plot comparison of ¹⁸F-FDG and ⁶⁸Ga-NODAGA-RGD SUV_max in organs. SUV_max was significantly different between both tracers in all organs (all p < 0.037), except in the thyroid, the gut (small intestine and colon), and the bladder (not shown) (all p > 0.10). The most significant difference was observed for the brain and the myocardium, which presented only minimal ⁶⁸Ga-NODAGA-RGD uptake compared to ¹⁸F-FDG