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. 2021 Dec 20;28(6):5466–5479. doi: 10.3390/curroncol28060455

Table 2.

Safety summary.

Patients with at Least 1, n (%) Arm B Arm C Arm D
Atezo + IFNα Atezo + PEG-IFNα Atezo + PEG-IFNα + Bev
(n = 65) (n = 6) (n = 45)
Treatment-emergent AE of any grade 65 (100) 6 (100) 45 (100)
Treatment-emergent AE with fatal outcome 3 (4.6) 0 1 (2.2)
Serious treatment-emergent AE 19 (29.2) 4 (66.7) 19 (42.2)
Treatment-emergent Grade 3–5 AE 25 (38.5) 3 (50.0) 28 (62.2)
AE leading to drug withdrawal
AE leading to atezo withdrawal 3 (4.6) 1 (16.7) 1 (2.2)
AE leading to IFNα withdrawal 3 (4.6)
AE leading to PEG-IFNα withdrawal 1 (16.7) 2 (4.4)
AE leading to bev withdrawal 8 (17.8)
AE leading to drug dose modification/interruption
AE leading to atezo dose interruption 13 (20.0) 2 (33.3) 7 (15.6)
AE leading to IFNα dose modification/interruption 7 (10.8)
AE leading to PEG-IFNα dose modification/interruption 2 (33.3) 6 (13.3)
AE leading to bev dose interruption 11 (24.4)

AE, adverse event; atezo, atezolizumab; bev, bevacizumab; IFNα, interferon-α; PEG, polyethylene glycol.