Table 2.
Natalizumab treatment characteristics.
Natalizumab treatment characteristics | |
---|---|
Treatment duration (N = 304), median (IQR), months | 58.7 (30.7–78.0) |
Temporary interruptions | |
Patients with interruptions (N = 304), n (%) | 45 (14.8) |
Number of interruptions (N = 45), median (IQR) | 1.0 (1.0–3.0) |
Length of interruptions (N = 45), median (IQR), months | 2.0 (1.0–4.0) |
Treatment permanent discontinuation | |
Patients with treatment discontinuation (N = 304), n (%) | 154 (50.7) |
Reasons for treatment discontinuation (N = 154)a, n (%) | |
Anti-JCV antibody positive | 91 (59.1) |
Patient’s decision | 62 (40.3) |
Physician’s decision | 49 (31.8) |
Natalizumab treatment duration concern | 17 (11.0) |
Pregnancy desire | 11 (7.1) |
Insufficient efficacy | 8 (5.2) |
Adverse event | 5 (3.2) |
Medication change from natalizumab | 5 (3.2) |
Tolerability problem other than adverse events | 4 (2.6) |
Prior immunosuppressive use | 3 (1.9) |
Tysabri antibody positive | 3 (1.9) |
PML | 2 (1.3) |
Moved out of the area | 2 (1.3) |
Malignancy/cancer | 1 (0.6) |
Death | 1 (0.6) |
Consent withdrawal | 1 (0.6) |
Patients receiving concomitant therapy for MS management (N = 304), n (%) | 59 (19.4) |
Methylprednisolone | 33 (10.9) |
Prednisone | 21 (6.9) |
Systemic corticosteroid (not specified) | 5 (1.6) |
Prednisolone | 1 (0.3) |
Note: IQR, interquartile range; JCV, John Cunningham virus; MS, multiple sclerosis; PML, progressive multifocal leukoencephalopathy
aMultiple reasons could apply.