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. 2017 Sep 21;102(11):1913–1922. doi: 10.3324/haematol.2017.173583

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Figure 2. — Secondary time-to-event endpoints for rituximab SC and rituximab IV (intent-to-treat population). Analyses presented are (A) progression-free survival, (B) event-free survival, (C) disease-free survival, and (D) overall survival. CI: confidence interval; DFS: disease-free survival; EFS: event-free survival; HR: hazard ratio; IV: intravenous; OS: overall survival; PFS, progression-free survival; SC: subcutaneous.