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Table 2 All-grade AEs occurring in ≥ 10% of patients and corresponding grades 3 and 4 AEs

From: Safety and efficacy of everolimus in Chinese patients with metastatic renal cell carcinoma resistant to vascular endothelial growth factor receptor-tyrosine kinase inhibitor therapy: an open-label phase 1b study

 

Everolimus 10 mg/day (n = 64)

AE, n (%)

All-grade

Grade 3

Grade 4

Anemia

41 (64)

10 (16)

3 (5)

Hypertriglyceridemia

35 (55)

4 (6)

0 (0)

Mouth ulceration

34 (53)

2 (3)

0 (0)

Hyperglycemia

33 (52)

8 (13)

0 (0)

Hypercholesterolemia

32 (50)

0 (0)

0 (0)

Pyrexia

26 (41)

1 (2)

0 (0)

Increased blood lactate dehydrogenase

24 (38)

1 (2)

1 (2)

Fatigue

20 (31)

1 (2)

0 (0)

Increased gamma-glutamyltransferase

20 (31)

7 (11)

0 (0)

Rash

20 (31)

0 (0)

0 (0)

Increased blood creatinine

19 (30)

0 (0)

1 (2)

Cough

18 (28)

0 (0)

0 (0)

Increased aspartate aminotransferase

17 (27)

0 (0)

0 (0)

Increased alanine aminotransferase

15 (23)

1 (2)

0 (0)

Epistaxis

15 (23)

1 (2)

0 (0)

Hypocalcemia

14 (22)

0 (0)

0 (0)

Interstitial lung disease

14 (22)

1 (2)

0 (0)

Leukopenia

14 (22)

0 (0)

0 (0)

Pruritus

14 (22)

0 (0)

0 (0)

Peripheral edema

13 (20)

2 (3)

0 (0)

Decreased platelet count

13 (20)

1 (2)

0 (0)

Diarrhea

12 (19)

1 (2)

0 (0)

Dyspnea

12 (19)

1 (2)

4 (6)

Increased blood alkaline phosphatase

11 (17)

1 (2)

0 (0)

Hypokalemia

11 (17)

0 (0)

3 (5)

Lymphopenia

10 (16)

4 (6)

0 (0)

Nasopharyngitis

9 (14)

0 (0)

0 (0)

Dizziness

8 (13)

0 (0)

0 (0)

Insomnia

8 (13)

0 (0)

0 (0)

Increased blood creatine phosphokinase

7 (11)

0 (0)

0 (0)

Decreased appetite

7 (11)

1 (2)

0 (0)

Decreased hemoglobin

7 (11)

2 (3)

0 (0)

Hyponatremia

7 (11)

5 (8)

0 (0)

Nausea

7 (11)

0 (0)

0 (0)

Upper respiratory tract infection

7 (11)

0 (0)

0 (0)

Increased white blood cell count

7 (11)

0 (0)

0 (0)

  1. AE, adverse event.