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. 2020 Jun 4;33:100594. doi: 10.1016/j.gore.2020.100594

Table 4.

Adverse events associated with trabectedin treatment.

Adverse event, n (%) Hematological toxicity
Overall Grade 1/2 Grade 3/4
Neutropenia 11 (30.5) 4 (11.1) 7 (19.4)
Anemia 9 (25.0) 7 (19.4) 2 (5.6)
Febrile neutropenia 2 (5.6) 0 (0.0) 2 (5.6)
Thrombocytopenia 1 (2.7) 0 (0.0) 1 (2.7)



Non-hematological toxicity
Fatigue 9 (25.0) 8 (22.2) 1 (2.7)
Nausea 5 (13.9) 5 (13.9) 0 (0.0)
Vomiting 4 (11.1) 4 (11.1) 0 (0.0)
Diarrhea 2 (5.6) 2 (5.6) 0 (0.0)
Decreased appetite 2 (5.6) 2 (5.6) 0 (0.0)
Elevation in ALT 2 (5.6) 2 (5.6) 0 (0.0)
Elevation in AST 1 (2.7) 1 (2.7) 1 (2.7)
Constipation 1 (2.7) 1 (2.7) 0 (0.0)
Myalgia 1 (2.7) 1 (2.7) 0 (0.0)
Hypotension 1 (2.7) 1 (2.7) 0 (0.0)
Hypocalcemia 1 (2.7) 1 (2.7) 0 (0.0)
Mucositis 1 (2.7) 1 (2.7) 0 (0.0)
Infection 1 (2.7) 0 (0.0) 1 (2.7)

ALT, alanine aminotransferase; AST, aspartate aminotransferase.