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Table 3 Description of the constraint period limited to duration of first stable modification*

From: Impact of imiglucerase supply constraint on the therapeutic management and course of disease in French patients with Gaucher disease type 1

 

Patients who discontinued imiglucerase (N = 61)

Patients receiving a reduced imiglucerase dose (N = 32)

Imiglucerase treatment

 

n

Median (range)

n

Median (range)

Time between treatment start and first modification (years)

 

9.7 (1; 14)

 

8.4 (1; 13)

Duration of the limited period of constraint (months)

 

5.1 (3; 15)

 

6.0 (3; 15)

Imiglucerase dose (U/kg/4-weeks):

    

At treatment initiation

58

118.5 (51; 246)

31

113.1 (58; 267)

At pre-constraint timepoint

56

89.4 (10; 223)

32

94.7 (46; 239)

At first modification

61

0.0 (0.0; 0.0)

32

52.4 (32; 181)

Dose decrease from pre-constraint dose (%):

  

n (%) patients

<25%

   

8 (25.0%)

≥25%; <50%

   

13 (40.6%)

≥50%; <75%

   

11 (34.4%)

Evolution of biological parameters

 

n

Slope Estimate (SE)

Time-effect (p-value)

n

Slope Estimate (SE)

Time-effect (p-value)

Hemoglobin (g/L)

47

−0.8 (0.2)

0.003

26

0.6 (0.4)

0.196

Platelets (103/mm)

47

−5905 (1721)

0.002

26

1762 (1720)

0.322

Serum ferritin (μg/L)

22

12.4 (6.4)

0.078

10

−3.4 (13.3)

0.812

Chitotriosidase (nmol/mL/h)

31

537 (208)

0.021

15

179 (259)

0.510

ACE (IU/L)

16

3.6 (1.1)

0.012

11

−2.8 (1.9)

0.228

Spontaneously reported GD-related events (by MedDRA Preferred Term)

 

Number (%) of patients

Number (%) of patients

All events

15 (24.6%)

7 (21.9%)

Bone events

  

   Bone infarction

1 (1.6%)

-

   Hand fracture

1 (1.6%)

-

Hematological events

  

   Thrombocytopenia

3 (4.9%)

1 (3.1%)

   Pancytopenia

1 (1.6%)

-

   Epistaxis

1 (1.6%)

1 (3.1%)

   Gingival bleeding

1 (1.6%)

-

   Hematoma

1 (1.6%)

-

Visceral events

  

   Hepatomegaly

-

1 (3.1%)

Other events

  

   Asthenia/ Fatigue

4 (6.6%)

3 (9.4%)

   Bone pain

2 (3.3%)

1 (3.1%)

   Musculoskeletal pain

-

1 (3.1%)

   Arthralgia

1 (1.6%)

-

   Serum ferritin increased

-

2 (6.3%)

   ACE increased

-

1 (3.1%)

   Chitotriosidase increased

1 (1.6%)

-

   Parkinson’s disease

1 (1.6%)

-

   Stress

1 (1.6%)

-

  1. *”First stable modification” refers to discontinuation or reduced dose for at least 3 consecutive months.
  2. Numerical values in bold print indicate statistical significance.