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. 2022 May 17;16:1483–1493. doi: 10.2147/DDDT.S358092

Table 2.

Summary of Treatment-Related Adverse Events in All Patients

Adverse Events Total (n=27) Combination Group (n=14) Monotherapy Group (n=13) P value*
Any Grade Grade 1–2 Grade 3 Any Grade Grade 1–2 Grade 3 Any Grade Grade 1–2 Grade 3
Anorexia 16 (59.26) 16 (59.26) 0 12 (85.71) 12 (85.71) 0 4 (30.77) 4 (30.77) 0 0.005
Thrombocytopenia 10 (37.04) 10 (37.04) 0 7 (50.00) 7 (50.00) 0 3 (23.08) 3 (23.08) 0 0.147
Hypertension 9 (33.33) 9 (33.33) 0 6 (42.86) 6 (42.86) 0 3 (23.08) 3 (23.08) 0 0.249
Diarrhoea 8 (29.63) 8 (29.63) 0 4 (28.57) 4 (28.57) 0 4 (30.77) 4 (30.77) 0 0.615
Fatigue 6 (22.22) 6 (22.22) 0 4 (28.57) 4 (28.57) 0 2 (15.38) 2 (15.38) 0 0.362
Anaemia 5 (18.52) 5 (18.52) 0 2 (14.29) 2 (14.29) 0 3 (23.08) 3 (23.08) 0 0.462
Proteinuria 3 (11.11) 3 (11.11) 0 2 (14.29) 2 (14.29) 0 1 (7.69) 1 (7.69) 0 0.529
Hand-foot syndrome 3 (11.11) 3 (11.11) 0 3 (21.43) 3 (21.43) 0 0 0 0 0.124
Bleeding 4 (14.71) 1 (3.70) 3 (11.11) 3 (21.43) 1 (7.14) 2 (14.29) 1 (7.69) 0 1 (7.69) 0.327

Notes: Data were expressed as n (%); *p value of any grade between combination and monotherapy group.