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. Author manuscript; available in PMC: 2019 Feb 7.
Published in final edited form as: Sci Transl Med. 2018 May 9;10(440):eaar5894. doi: 10.1126/scitranslmed.aar5894

Figure 2. The tumor clone frequency in skin as predictor of progression-free and overall survival in patients with cutaneous T cell lymphomas.

Figure 2.

A. Kaplan-Meier estimates of progression-free (left panel) and overall survival (right) in 208 patients with cutaneous T cell lymphomas in the discovery set, according to the tumor clone frequency in skin (<25% versus >25% of the total T cells in skin). B. Kaplan-Meier estimates of progression-free survival in 101 patients with cutaneous T cell lymphomas in the validation set, according to the tumor clone frequency in skin (<25% versus >25% of the total T cells in skin). C. Kaplan-Meier estimates of progression-free (left panel) and overall survival (right) in 177 patients with mycosis fungoides in the discovery set, according to the tumor clone frequency in skin (<25% versus >25% of the total T cells in skin). D. Kaplan-Meier estimates of progression-free survival in 87 patients with mycosis fungoides in the validation set, according to the tumor clone frequency in skin (<25% versus >25% of the total T cells in skin). p-values in A-D are estimated by Cox univariable analysis. E. Kaplan-Meier estimates of progression-free (left panel) and overall survival (right) in 22 patients with Sézary syndrome in the discovery set, according to the tumor clone frequency in skin (<25% versus >25% of the total T cells in skin).