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Table 3 Treatment-related adverse events

From: Venetoclax Combined with Azacitidine and Homoharringtonine in Relapsed/Refractory AML: A Multicenter, Phase 2 Trial

 

Grade 1–2

Grade 3

Grade 4

Grade 5

Adverse event (n = 96)

Anemia

16 (16.7)

62 (64.6)

2 (2.1)

0

Neutropenia

6 (6.3)

60 (62.5)

19 (19.8)

0

Thrombocytopenia

8 (8.3)

14 (14.6)

58 (60.4)

0

Febrile neutropenia

0

25 (26.0)

10 (10.4)

1 (1.0)

Pneumonia

1 (1.0)

15 (15.6)

6 (6.3)

1 (1.0)

Sepsis

0

0

10 (10.4)

1 (1.0)

Nausea

20 (22.9)

3 (3.1)

0

0

Constipation

12 (12.5)

0

0

0

Diarrhea

11 (11.5)

0

0

0

Vomiting

10 (10.4)

2 (2.1)

0

0

Decreased appetite

22 (22.9)

2 (2.1)

0

0

Hypokalemia

13 (13.5)

5 (5.2)

1 (1.0)

0

Peripheral edema

10 (10.4)

1 (1.0)

0

0

Fatigue

23 (24.0)

2 (2.1)

0

0

Mucositis

8 (8.3)

4 (4.2)

0

0

Colitis

5 (5.2)

1 (1.0)

0

0

Cough

11 (11.5)

1 (1.0)

0

0

Muscle weakness

0

1 (1.0)

0

0

Hyperbilirubinemia

9 (9.4)

3 (3.1)

0

0

ALT or AST elevation

12 (12.5)

4 (4.2)

0

0

Allergic reaction

3 (3.7)

1 (1.0)

0

0

Heart failure

1 (1.0)

2 (2.1)

1 (1.0)

1 (1.0)

Renal failure

0

0

1 (1.0)

0

Tumor lysis syndrome

0

1 (1.0)

1 (1.0)

0

  1. All patients in the safety population included (n = 96). Toxicity grades are according to the Common Terminology Criteria for Adverse Events version 4.03. Listed toxicities include both those attributable to therapy and those deemed not attributable to therapy. Data are n (%)