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Table 3 Patients with dose-limiting toxicity events

From: A phase 1b study of humanized KS-interleukin-2 (huKS-IL2) immunocytokine with cyclophosphamide in patients with EpCAM-positive advanced solid tumors

huKS-IL2 dosing cohort, mg/m2

Patient age, years

DLT

AE gradea

Day started (cycle)

Duration, days

DLT outcome

2.0

63

Hypoxia

3

2 (1)

2

Recovered

3.0

59

Dyspnea

3

3 (1)

25

Recovered

Bronchospasm

3

4 (1)

2

Recovered

GGT increased

3

4 (1)

19

Recovered

4.0

55

Thrombocytopenia

4

8 (1)

3

Recovered

Neutropenia

3

8 (1)

3

Recovered

63

Anemiab

3

5 (1)

2

Recovered

  1. a National Cancer Institute Common Terminology Criteria for Adverse Events grade.
  2. b Patient entered study with anemia, but was hospitalized after dosing for a blood transfusion.
  3. DLT, dose-limiting toxicity; GGT, gamma-glutamyltransferase; huKS-IL2, humanized KS-interleukin-2.