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Table 3 Summary of safety (AEs by preferred term reported by ≥ 5% of patients; safety population)

From: A randomized, open-label, Phase III study of obinutuzumab or rituximab plus CHOP in patients with previously untreated diffuse large B-Cell lymphoma: final analysis of GOYA

Variable

R-CHOP (N = 701) n (%)

G-CHOP (N = 702) n (%)

No. of deaths (any reason)

141 (20.1)

149 (21.2)

No. of patients withdrawn from the study due to an AE

4 (0.6)

6 (0.9)

Patients with ≥ 1

 AE

659 (94.0)

685 (97.6)

 Grade 3–5 AE

461 (65.8)

527 (75.1)

 AE with fatal outcomea

31 (4.4)

43 (6.1)

 Serious AE

269 (38.4)

312 (44.4)

 Treatment-related AE

600 (85.6)

647 (92.2)

 AE leading to withdrawal of any treatment

58 (8.3)

8.7 (12.4)

 AE leading to dose reduction for any treatment

142 (20.3)

145 (20.7)

 

Grade 3–5 AE, n (%)

Serious AE, n (%)

Grade 3–5 AE, n (%)

Serious AE, n (%)

 Blood and lymphatic system disorders

  Neutropenia

277 (39.5)

38 (5.4)

336 (47.9)

54 (7.7)

  Febrile neutropenia

108 (15.4)

71 (10.1)

130 (18.5)

85 (12.1)

  Leukopenia

78 (11.1)

104 (14.8)

  Anemia

55 (7.8)

53 (7.5)

  Thrombocytopenia

11 (1.6)

40 (5.7)

 Infections and infestations

  Pneumonia

34 (4.9)

33 (4.7)

44 (6.3)

43 (6.1)

  1. AE adverse event, G-CHOP obinutuzumab plus cyclophosphamide, doxorubicin, vincristine, and prednisone, R-CHOP rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone
  2. aFatal AEs that occurred in more than one patient in either group, listed as preferred terms, were as follows: death (cause unknown; 2 patients in the R-CHOP arm and 3 patients in the G-CHOP arm), pneumonia (5 patients in each arm), septic shock (6 patients in the G-CHOP arm), sepsis (3 patients in the R-CHOP arm and 1 patient in the G-CHOP arm), hepatocellular carcinoma (1 patient in the R-CHOP arm and 2 patients in the G-CHOP arm), cerebrovascular accident (2 patients in each arm), and pulmonary embolism (2 patients in the G-CHOP group)