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. 2022 Jul 8;29(7):4799–4810. doi: 10.3390/curroncol29070381

Table 4.

Adverse events associated with ATZ + BV treatment.

Adverse Events Grade 1 or 2 Grade 3 Any Grade (%)
Pyrexia 12 0 12 (42.9)
Fatigue 4 5 9 (32.1)
Increased TSH 7 0 7 (25.0)
Liver disfunction 6 1 * 7 (25.0)
Renal disfunction 6 0 6 (21.4)
Rash 4 1 * 5 (17.9)
Proteinuria 3 1 4 (14.3)
Decreased appetite 3 1 4 (14.3)
Hypertension 3 1 4 (14.3)
Stomatitis 3 0 3 (10.7)
Ascites 3 0 3 (10.7)
Edema 3 0 3 (10.7)
Diarrhea 2 1 3 (10.7)
Dicreased TSH 2 0 2 (7.1)
Palmar–plantar erythrodysesthesia 2 0 2 (7.1)
Oral mucositis 0 2 * 2 (7.1)
Heart failure 1 0 1 (3.6)
Infusion reaction 1 0 1 (3.6)
Acute adrenal insufficiency 0 1 * 1 (3.6)
Hemophagocytic syndrome 0 1 * 1 (3.6)

Values are expressed as a number in grade 1 and 2 and grade 3 categories. Values are expressed as number (%) in any grade category. * These cases were treated with steroid therapy due to severe irAEs. TSH—thyroid-stimulating hormone; ATZ—atezolizumab; BEV—bevacizumab; irAE—immune-related adverse event.