Correction: Acta Neuropathologica Communications (2024) 12:77 https://doi.org/10.1186/s40478-024-01790-3
Following the publication of the original article [1], the wrong figure appeared as Fig. 7; the figure should have appeared as shown below.
Verification of the constructed prognostic model for PFS prediction in two testing sets (the TCGA and G-SAM datasets). A Correlation between the PFI values and the risk scores estimated by the constructed model for the primary IDH-wt GBM cases in the TCGA and G-SAM cohorts. B Kaplan–Meier analyses of PFS for the groups with low- or high-risk scores in the TCGA and G-SAM cohorts. C Time-dependent ROC analyses of 1-, 2-, and 3-year PFS for the constructed model in the TCGA and G-SAM cohorts. D Construction of a nomogram for quantitatively predicting 1-, 2-, and 3-year PFS of primary IDH-wt GBM patients
The original article has been corrected.
Reference
Ho WM, Chen CY, Chiang TW et al (2024) A longer time to relapse is associated with a larger increase in differences between paired primary and recurrent IDH wild-type glioblastomas at both the transcriptomic and genomic levels. Acta Neuropathol Commun 12:77. https://doi.org/10.1186/s40478-024-01790-3
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Ho, WM., Chen, CY., Chiang, TW. et al. Correction: A longer time to relapse is associated with a larger increase in differences between paired primary and recurrent IDH wild-type glioblastomas at both the transcriptomic and genomic levels. acta neuropathol commun 12, 119 (2024). https://doi.org/10.1186/s40478-024-01829-5
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DOI: https://doi.org/10.1186/s40478-024-01829-5