Fig. 3: Comprehensive clinical-methylomic nomogram that predicted BM development from LUAD tissues. | Nature Medicine

Fig. 3: Comprehensive clinical-methylomic nomogram that predicted BM development from LUAD tissues.

From: Prediction of brain metastasis development with DNA methylation signatures

Fig. 3

a, Point calculator diagram assigning point values to methylome and TNM scores, followed by the nomogram that uses total summed point values to derive composite probabilities of 5-year BM development. b, Kaplan–Meier plot and log-rank test of high-risk and low-risk nomogram scores, based on the median, demonstrating in the independent validation dataset that high-risk scores capture most of the early BM events plus BM that occurs within 5 years, while most low-risk scores occur in patients who do not develop BM early or within 5 years. c, Results of the univariable Cox proportional hazards model using nomogram scores demonstrating the significantly increased BM risk with increasing nomogram score (n = 60). The box with the whiskers displays the HR and 95% CI. d, Time-dependent mean AUROC with associated 95% CI in the validation cohort, using a bootstrap resampling approach to derive nomogram scores, showing accurate differentiation of patients who developed BM within 5 years (n = 42). The box with the whiskers displays the AUROC and 95% CI. * denotes a significant P value.

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