Table 2

Treatment-related adverse events of any grade in 5% or more in the overall population of 61 patients

Adverse eventDecitabine-plus-camrelizumab (n=42)Camrelizumab (n=19)
Any gradeGrade 3–4Any gradeGrade 3–4
Any adverse event41 (98)9 (21)19 (100)3 (16)
Reactive capillary endothelial proliferation36 (86)016 (84)0
Leukocytopenia26 (62)9 (21)6 (32)0
Fever16 (38)06 (32)2 (11)
Pain in the lesion8 (19)03 (16)0
Increased triglyceride6 (14)02 (11)0
Rash5 (12)00 (0)0
Pneumonitis4 (10)1 (2)1 (5)1 (5)
Diarrhea4 (10)000
Myalgia4 (10)00 (0)0
Increased transaminase3 (7)03 (16)0
Hypothyroidism3 (7)03 (16)0
Increased UA3 (7)01 (5)0
Myocardial ischemia3 (7)000
Nausea3 (7)000
Thrombocytosis2 (5)000
Fatigue1 (2)02 (11)0
Thrombocytopenia1 (2)01 (5)0
  • UA, Uric Acid.