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. 2023 Feb 6;13:1113462. doi: 10.3389/fonc.2023.1113462

Table 2.

Incidence of nonhematologic adverse events reported for dasatinib treatment.

Adverse events Patients (%)
First-line Second-line
Dasatinib 100mg daily Dasatinib 100mg daily
Any Grade Grade 3/4 Any Grade Grade 3/4
Hematologic toxicity
Neutropenia 7-64 6-29 12-64 12-63
Leukopenia 4 1 8-61 1-24
Anemia 13-90 3-13 23-91 6-20
Thrombocytopenia 18-70 9-22 23-65 11-57
Non-hematologic toxicity
Gastrointestinal toxicity
Diarrhea 17-59 0-5 9-37 0-3
Nausea 8-52 0-3 18-27 0-1
Vomiting 5-30 0-2 10 8 2 7 0-1
Abdominal pain 17 3 15 3 12 0-1
Musculoskeletal toxicity
Muscle spasms 5-8 <1 1 0
Myalgia 6 <1 13-37.6 0-1.8
Musculoskeletal pain 11-69 <8 19-21 1-2
Cutaneous disorder
Rash 11-27 0 8-32.8 0-3
Metabolic disorders
Hyperlipidemia NR NR NR NR
Hyperglycemia 13 1 NR NR
Hepatotoxicity 26 1 NR NR
Nephrotoxicity 17 2 NR NR
General Disorders
Headache 12-48 0-5 15-33 1-2
Fatigue 8-76 1-13 2-37 0-4
Pulmonary disorders
Pleural effusions 10-35 0-9 9-26 2-8
Pulmonary arterial hypertension 2.6-5 0-1 2.4 1.1
Cardiovascular Toxicity
QTc prolongation 1.6-73 NR NR NR
Arterial vascular events 5 0-1 4 0-1

NR, not reported.