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. 2016 Aug 15;34(29):3562–3569. doi: 10.1200/JCO.2016.68.1106

Table 2.

Treatment-Related AEs

AE Cohort (µg/kg), No. (%)
Grade 1 to 2 Grade 3 to 4
1
(n = 4) 2.5
(n = 6) 5
(n = 6) 10
(n = 6) 20
(n = 6) 40
(n = 5) 1
(n = 4) 2.5
(n = 6) 5
(n = 6) 10
(n = 6) 20
(n = 6) 40
(n = 5)
Hematologic
 Anemia 1 (17) 4 (67) 2 (33) 2 (33) 3 (60) 1 (25) 1 (17) 2 (33) 1 (17)
 Leukopenia 1 (17) 1 (17)
 Thrombocytopenia 1 (17) 3 (50) 2 (33) 3 (50) 4 (80) 1 (17)
Nonhematologic
 ALT increased 2 (40)
 Anorexia 1 (25) 1 (17) 1 (17) 3 (50) 2 (33) 2 (40)
 Arthralgia 1 (17) 1 (20)
 Back pain 1 (17) 1 (20)
 Chills 1 (17) 3 (50) 1 (20)
 Diarrhea 1 (17) 1 (17) 1 (20)
 Dyslipidemia 1 (25) 1 (17) 1 (20)
 Fatigue 1 (17) 4 (67) 2 (33) 4 (67) 4 (80)
 Fever 1 (25) 1 (17) 2 (33) 1 (17) 3 (50) 2 (40)
 Flu-like symptoms 1 (17) 1 (17) 1 (17) 1 (17) 1 (20)
 Hypoalbuminemia 1 (17) 1 (20)
 Increased lipase 1 (20)
 Injection site reaction 2 (50) 3 (50) 3 (50) 2 (33) 2 (40)
 Myalgia 1 (17) 1 (17)
 Nausea 2 (50) 1 (17) 1 (17) 2 (33) 1 (17)
 Night sweats 1 (17) 1 (17)
 Pruritis 1 (17) 1 (17) 2 (33)
 Rash/rash maculopapular 1 (17) 4 (67) 2 (40)
 Transaminitis 1 (20)
 Vomiting 1 (25) 1 (17) 1 (17)
 Weakness 2 (33) 1 (17) 1 (20)

NOTE. Does not include events that occurred in < two patients at grade 1 to 2 severity.

Abbreviation: AE, adverse event.