Table 2 Highest grade treatment-related Adverse Events (trAE) occurring in ≥10% of patients receiving ENMD-2076.

From: A phase II study of ENMD-2076 in advanced soft tissue sarcoma (STS)

CTCAE v4.0 classification

Any grade N (%)

Grade 3/4 N (%)

Hypertension

17 (68)

15 (60)

Fatigue

16 (64)

0 (0)

Diarrhea

15 (52)

1 (4)

ALT Increased

12 (48)

2 (8)

Hypoalbuminemia

12 (48)

0 (0)

Proteinuria

12 (48)

0 (0)

Dyspepsia

11 (44)

0 (0)

Lymphopenia

11 (44)

0 (0)

Nausea

11 (44)

0 (0)

Thrombocytopenia

10 (40)

1 (4)

AST Increased

9 (36)

1 (4)

Constipation

8 (32)

0 (0)

Xerostomia

8 (32)

0 (0)

Dizziness

7 (28)

0 (0)

Hyponatremia

7 (28)

1 (4)

Mucositis oral

7 (28)

0 (0)

ALP Increased

6 (24)

0 (0)

Headache

6 (24)

0 (0)

Anemia

5 (20)

1 (4)

White blood cell decreased

5 (20)

1 (4)

Edema

4 (16)

0 (0)

Glucose intolerance

4 (16)

0 (0)

Hematuria

4 (16)

0 (0)

Hypomagnesemia

4 (16)

0 (0)

Vomiting

4 (16)

0 (0)

Abdominal pain

3 (12)

0 (0)

Dysgeusia

3 (12)

0 (0)

Flatulence

3 (12)

0 (0)

Hoarseness

3 (12)

0 (0)

Hyperuricemia

3 (12)

0 (0)

Neutrophil count decreased

3 (12)

1 (4)

Palmar-plantar erythrodysesthesia syndrome

3 (12)

0 (0)

Rash maculo-papular

3 (12)

0 (0)

UTI

3 (12)

0 (0)

  1. aEvents considered at least possibly related to study treatment. Patients may appear in the table more than once.
  2. Abbreviations – CTCAE, Common terminology criteria for adverse events; ALT, alanine aminotransferase; ALP, Alkaline phosphatase; UTI, Urinary Tract Infection.