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Table 6 Occurrence of haematological Grade 3–4 adverse events across treatment cycles

From: Azacitidine improves clinical outcomes in older patients with acute myeloid leukaemia with myelodysplasia-related changes compared with conventional care regimens

Preferred term

Cycles 1–2

Cycles 3–4

Cycles 5–6

Cycles 7+

AZA (N = 128)

CCR (N = 130)

AZA (n = 89)

CCR (n = 61)

AZA (n = 75)

CCR (n = 25)

AZA (n = 57)

CCR (n = 17)

Any Grade 3–4 TEAE, n (%)

83 (65)

99 (76)

47 (53)

35 (57)

33 (44)

8 (32)

37 (65)

13 (77)

Febrile Neutropenia, n (%)

23 (18)

34 (26)

7 (8)

7 (12)

4 (5)

3 (12)

3 (5)

2 (12)

Thrombocytopenia, n (%)

24 (19)

26 (20)

11 (12)

8 (13)

8 (11)

0

9 (16)

0

Neutropenia, n (%)

16 (13)

20 (15)

10 (11)

9 (15)

3 (4)

2 (8)

12 (21)

5 (29)

Anaemia, n (%)

17 (13)

21 (16)

3 (3)

3 (5)

1 (1)

0

5 (9)

0

  1. Safety evaluable patients received at least 1 dose of study drug and had at least 1 post-baseline safety assessment. Patients who received BSC only were included in safety assessments if they had at least 1 post-randomisation safety assessment