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Table 2 Incidence of hematologic adverse events before/after palbociclib dose reduction from 125 to 100 mg

From: Hematologic adverse events following palbociclib dose reduction in patients with hormone receptor–positive/human epidermal growth factor receptor 2–negative advanced breast cancer: pooled analysis from randomized phase 2 and 3 studies

Adverse event

Before dose reduction (N = 311)

After dose reduction

Cycle 1 (N = 310)

Cycle 2 (N = 284)

Cycle 3 (N = 267)

Cycle 4 (N = 253)

Cycle 5 (N = 241)

Cycle 6 (N = 228)

Grade, n (%)

Grade, n (%)

Grade, n (%)

Grade, n (%)

Grade, n (%)

Grade, n (%)

Grade, n (%)

All

3

4

All

3

4

All

3

4

All

3

4

All

3

4

All

3

4

All

3

4

Leukopenia*

130 (41.8)

86 (27.7)

2 (0.6)

88 (28.4)

25 (8.1)

0

83 (29.2)

22 (7.7)

0

71 (26.6)

22 (8.2)

0

64 (25.3)

17 (6.7)

0

60 (24.9)

12 (5.0)

0

56 (24.6)

15 (6.6)

0

Thrombocytopenia

48 (15.4)

5 (1.6)

1 (0.3)

36 (11.6)

3 (1.0)

0

29 (10.2)

3 (1.1)

0

23 (8.6)

2 (0.7)

0

21 (8.3)

2 (0.8)

0

20 (8.3)

0

0

20 (8.8)

1 (0.4)

0

Anemia

38 (12.2)

8 (2.6)

0

55 (17.7)

5 (1.6)

0

54 (19.0)

3 (1.1)

0

49 (18.4)

2 (0.7)

0

43 (17.0)

2 (0.8)

0

38 (15.8)

2 (0.8)

0

39 (17.1)

1 (0.4)

0

Febrile neutropenia

7 (2.3)

6 (1.9)

1 (0.3)

0

0

0

0

0

0

0

0

0

0

0

0

1 (0.4)

1 (0.4)

0

0

0

0

  1. *Leukopenia includes the following preferred terms: leukopenia or white blood cell count decreased
  2. Thrombocytopenia includes the following preferred terms: platelet count decreased or thrombocytopenia
  3. Anemia includes the following preferred terms: anemia or hematocrit decreased or hemoglobin decreased