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Table 3 Everolimus/Sirolimus-related adverse events

From: Everolimus versus sirolimus for angiomyolipoma associated with tuberous sclerosis complex: a multi-institutional retrospective study in China

 

Sirolimus n = 33 (%)

Everolimus n = 91 (%)

P-value

All grades

All grades

Grade 3–4

All grades

Grade 3–4

Gastrointestinal

 Mucositis oral

30 (91)

4 (12)

89 (98)

11 (12)

0.23

 Diarrhea

4 (12)

0

5 (5)

0

0.39

 Vomiting

0

0

3 (3)

0

0.69

 Constipation

2 (6)

0

1 (1)

0

0.35

Gynaecological

 Irregular menstruation (female)

7 (30)

3 (13)

25 (44)

9 (15)

0.27

Metabolic

 Hypertriglyceridemia

11 (33)

0

30 (33)

0

0.97

 Cholesterol high

4 (12)

0

11 (12)

0

0.76

 Proteinuria

2 (6)

0

8 (9)

0

0.90

 ALP increased

4 (12)

0

8 (9)

0

0.83

 GGT increased

2 (6)

0

5 (5)

0

0.75

 Hypophosphatemia

0

0

3 (3)

0

0.69

Infection

 Upper respiratory infection

11 (33)

0

22 (24)

0

0.31

 Pneumonitis

4 (12)

2 (6)

5 (6)

3 (3)

0.39

 Urinary tract infection

4 (12)

0

5 (6)

0

0.39

Dermatology

 Rash acneiform

6 (18)

0

16 (18)

3 (3)

0.94

Constitutional symptoms

 Abdominal pain

4 (12)

0

11 (12)

0

0.76

 Headache

4 (12)

0

3 (3)

0

0.15

 Malaise

2 (6)

0

3 (3)

0

0.86

Soft tissues

 Peripheral oedema

4 (12)

2 (6)

3 (3)

0

0.15

Blood

 Neutrophil count decreased

2 (6)

0

3 (3)

0

0.86

 Lymphocyte count decreased

0

0

3 (3)

0

0.69

 Anemia

2 (6)

0

1 (1)

0

0.35

  1. Everolimus/Sirolimus-related adverse reactions were those adverse events that were considered to be possibly or definitely related to everolimus/sirolimus