Table 4 Incidence of TEAEs of interest by time to new onset for ibrutinib+BR-treated patients

From: Updated results from the phase 3 HELIOS study of ibrutinib, bendamustine, and rituximab in relapsed chronic lymphocytic leukemia/small lymphocytic lymphoma

TEAE, n (%)

0–1 year (n = 287)

1–2 years (n = 216)

2–3 years (n = 188)

 > 3 years (n = 83)

Infection

190 (66.2)

22 (10.2)

4 (2.1)

1 (1.2)

Neutropenia

164 (57.1)

3 (1.4)

0

0

Nausea

105 (36.6)

1 (0.5)

0

0

Diarrhea

98 (34.1)

9 (4.2)

1 (0.5)

2 (2.4)

Thrombocytopenia

86 (30.0)

2 (0.9)

1 (0.5)

0

Bleeding

84 (29.3)

10 (4.6)

4 (2.1)

1 (1.2)

Pyrexia

69 (24.0)

5 (2.3)

4 (2.1)

0

Anemia

64 (22.3)

2 (0.9)

2 (1.1)

0

Fatigue

58 (20.2)

5 (2.3)

3 (1.6)

1 (1.2)

Cough

48 (16.7)

12 (5.6)

4 (2.1)

1 (1.2)

Pneumonia

38 (13.2)

15 (6.9)

7 (3.7)

1 (1.2)

Upper respiratory tract infection

38 (13.2)

17 (7.9)

4 (2.1)

2 (2.4)

Hypertension

27 (9.4)

8 (3.7)

4 (2.1)

0

Atrial fibrillation/flutter

19 (6.6)

4 (1.9)

6 (3.2)

0

  1. TEAE treatment-emergent adverse event