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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: Clin Cancer Res. 2021 Feb 26;27(11):2996–3004. doi: 10.1158/1078-0432.CCR-21-0066

Table 3:

Grade 3 to 5 Adverse Events Possibly, Probably, or Definitely Associated with Study Treatment

Toxicity Type Subprotocol
EAY131-Z1A (n=50)
Grade
3 4 5
(n) (n) (n)
Heart failure 1 - -
Myocardial infarction 1 - -
Eye disorders 1 - -
Mucositis oral 1 - -
Nausea 1 - -
Small intestinal obstruction 1 - -
Fatigue 1 - -
Multi-organ failure - - 1
Edema limbs 1 - -
Urinary tract infection 1 - -
Alanine aminotransferase increased 1 - -
Alkaline phosphatase increased 1 - -
Aspartate aminotransferase increased 1 - -
CPK increased 2 - -
Lymphocyte count decreased 2 - -
White blood cell decreased 1 - -
Ejection fraction decreased 1 - -
Anorexia 1 - -
Dehydration 1 - -
Hypoalbuminemia 1 - -
Hyponatremia 1 - -
Hypophosphatemia 1 - -
Muscle weakness lower limb 1 - -
Muscle weakness upper limb 1 - -
Syncope 1 - -
Rash acneiform 3 - -
Skin and subcutaneous tissue disorders 1 - -
Hypertension 6 - -