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. 2023 Jan 3;23:2. doi: 10.1186/s12886-022-02723-1

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© The Author(s) 2023

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. 5 — Clinical correlations in the TCGA UVM dataset. The risk score distributions between the signature risk scores and the clinicopathological features in different subgroups: (A) histological subtypes (single vs mixed subtype; p = 0.041) (single: spindle cell subtype and epithelioid cell subtype; mixed: Epithelioid Cell | Spindle Cell, and Spindle Cell | Epithelioid Cell); (B) TNM stage (stage II + III vs stage IV; p = 0.006); (C) T stage (T 2 + 3 vs T 4; p = 0.009); (D) M stage (M0 vs M1; p = 0.019); (E) new tumor event (NTE, NO vs YES, p = 8.317e-07); (F) tumor basal diameter (TBD, ≥ 15 vs < 15, p = 0.004); (G) age (≥ 65 vs < 65; p = 0.412); (H) gender (female vs male; p = 0.354)