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Table 1 (abstract O07). Assessment of drug response in the patients with colchicine resistant familial Mediterranean fever

From: Abstracts from the ISSAID 2021 Periodic Congress

 

Baseline

(n=114)

1st month

(n=114)

3rd month

(n=114)

6th month

(n=114)

12th month

(n=114)

18th month

(n=114)

24th month

(n=114)

PGA*

8 (5-10)

1 (0-10)

0 (0-5)

0 (0-5)

0 (0-3)

0 (0-5)

0 (0-3)

CRP*

16.2 (11-31)

0.65 (0.02-58.6)

0.2 (0-15.8)

0.7 (0-68)

0.5 (0-24.9)

0.3 (0-41)

0.3 (0.16.1)

SAA*

89 (2.9-1870)

3.9 (0-17)

4 (0-23)

3.3 (0-70)

3.6 (0-152)

3 (0-42)

3 (0-24)

Dose interval of CAN (weeks)

4 (4-8)

4 weeks in 94

8 weeks in 20

4 (4-8)

4 weeks in 94

8 weeks in 20

4 (4-8)

4 weeks in 94

8 weeks in 20

6 (4-8)

4 weeks in 66

6 weeks in 21

8 weeks in 27

6 (4-8)

4 weeks in 50

6 weeks in 21

8 weeks in 41

12 weeks in 2

8 (4-12)

4 weeks in 45

6 weeks in 21

8 weeks in 40

12 weeks in 3

No drug in 5

8 (4-12)

4 weeks in 39

6 weeks in 25

8 weeks in 38

No drug in 12

Dosage of CAN (mg/kg)

2-4 mg/kg

2-4 mg/kg

2-4 mg/kg

2-4 mg/kg

2-4 mg/kg

2-4 mg/kg

2-4 mg/kg

Number of patients experienced attacks

NA

0

2

1

5

4

2

Number of patients requiring higher dose or shortening drug interval

NA

0

2

(recurrent attacks)

0

2 (recurrent attacks)

4 (recurrent attacks)

(shortened from 8  to 6 weeks

2 (recurrent attacks, CAN was restarted)

Number of patients whose prolonged drug interval

NA

0

7 patients

(prolonged from 4 to 8 weeks)

21 patients

(prolonged from 4 to 6 weeks)

16 patients

(prolonged from 4 to 8 weeks)

2 patients (prolonged from 8 to 12 weeks)

5 patients (prolonged from 4 to 8 weeks)

1 patient (prolonged from 8 to 12 weeks)

6 patients

(prolonged from 4 to 8 weeks)

NA

Number of patients discontinued CAN

0

0

0

0

5 patients

7 patients

0

Number of infections

NA

1 (pneumonia)

1 (upper respiratory tract infection)

0

0

0

2 (upper respiratory tract infection)

Number of adverse event

NA

0

0

0

0

0

0