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. 2021 May 27;21:622. doi: 10.1186/s12885-021-08373-8

Table 3.

Adverse events in the two groups

Event IC* (n = 98) IC + immunotherapy (n = 65) p#
Grade 1–2 Grade 3–4 Grade 1–2 Grade 3–4
Anorexia 57 (58.2%) 0 40 (61.5%) 0
Nausea 40 (40.8%) 0 24 (36.9%) 0
Fatigue 30 (30.6%) 0 23 (35.4%) 0
Constipation 25 (25.5%) 0 18 (27.7%) 0
Stomatitis 17 (17.3%) 0 17 (26.2%) 0
Diarrhea 15 (15.3%) 0 13 (20.0%) 0
Neutropenia 12 (12.2%) 10 (10.2%) 10 (15.4%) 4 (6.2%)
Thrombocytopenia 11 (11.2%) 6 (6.1%) 10 (15.4%) 4 (6.2%)
Vomiting 8 (8.2%) 0 6 (9.2%) 0
Peripheral neuropathy 7 (7.1%) 0 6 (9.2%) 0
Liver dysfunction 7 (7.1%) 0 6 (9.2%) 0
Hypothyroidism 7 (7.1%) 0 6 (9.2%) 0
Venous thrombosis 2 (2.0%) 2 (2.0%) 2 (3.1%) 2 (3.1%)
Dizziness 2 (2.0%) 0 2 (3.1%) 0
Cough 1 (1.0%) 0 0 0 0.596

* IC induction chemotherapy

#: the p value indicated the difference of the events of grade 3–4 between the two groups