Adverse events | Experimental group (N = 40) | Control group (N = 18) | 合计(N = 58) |
---|---|---|---|
At least one adverse reaction occurred | 22 (55.00%) | 17 (94.44%) | 39 (67.24%) |
χ2 | 8.77 | ||
P | 0.003 | ||
Vomiting | 17 (42.50%) | 10 (55.56%) | 27 (46.55%) |
Bone marrow suppression | 8 (20.00%) | 12 (66.67%) | 20 (34.48%) |
diarrhea | 5 (12.50%) | 0 (0.00%) | 5 (8.62%) |
Fever | 1 (2.50%) | 2 (11.11%) | 3 (5.17%) |
Anemia | 1 (2.50%) | 1 (5.56%) | 2 (3.45%) |
Hypokalemia | 1 (2.50%) | 0 (0.00%) | 1 (1.72%) |
Myocardial ischemia | 0 (0.00%) | 1 (5.56%) | 1 (1.72%) |
dizziness | 1 (2.50%) | 0 (0.00%) | 1 (1.72%) |
Decreased platelets | 1 (2.50%) | 0 (0.00%) | 1 (1.72%) |