Table 5 Adverse events with an incidence of 10% or more in the phase Ib safety population, regardless of relationship to study drugs*

From: Afuresertib plus fulvestrant for pretreated HR-positive, HER2-negative, advanced breast cancer: a phase Ib trial

 

N = 31

 

Any grade

Grade 3 or higher

Hyperglycemia

16(51.6)

0

Diarrhea

14(45.2)

3(9.7)

Rash

13(41.9)

1(3.2)

Aspartate aminotransferase increased

12(38.7)

2(6.5)

Hypercholesterolemia

11(35.5)

0

Alanine aminotransferase increased

9(29.0)

2(6.5)

Anemia

9(29.0)

0

Weight decreased

8(25.8)

0

Nausea

7(22.6)

0

Blood creatinine increased

6(19.4)

0

COVID-19

6(19.4)

0

Hypophosphatasemia

6(19.4)

0

Hypertriglyceridemia

5(16.1)

1(3.2)

Hypokalemia

5(16.1)

0

Proteinuria

5(16.1)

0

Upper respiratory tract infection

5(16.1)

0

Urinary tract infection

5(16.1)

0

Blood cholesterol increased

4(12.9)

0

Cough

4(12.9)

0

  1. *Adverse events were assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE), version 5.0, and coded to a preferred term using the latest version of Medical Dictionary for Regulatory Activities (MedDRA).