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Predicting long-term disability outcomes in patients with MS treated with teriflunomide in TEMSO
被引:13
|作者:
Sormani, Maria Pia
[1
]
Truffinet, Philippe
[2
]
Thangavelu, Karthinathan
[3
]
Rufi, Pascal
[2
]
Simonson, Catherine
[4
]
De Stefano, Nicola
[5
]
机构:
[1] Univ Genoa, Biostat Unit, Genoa, Italy
[2] Sanofi Genzyme, Chilly Mazarin, France
[3] Sanofi Genzyme, Cambridge, MA USA
[4] Fishawack Commun Ltd, Abingdon, Oxon, England
[5] Univ Siena, Dept Med Surg & Neurosci, Siena, Italy
来源:
关键词:
RELAPSING MULTIPLE-SCLEROSIS;
INTERFERON-BETA;
GLATIRAMER ACETATE;
DISEASE-ACTIVITY;
SCORE;
D O I:
10.1212/NXI.0000000000000379
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Objective: To predict long-term disability outcomes in TEMSO core (NCT00134563) and extension (NCT00803049) studies in patients with relapsing forms of MS treated with teriflunomide. Methods: A post hoc analysis was conducted in a subgroup of patients who received teriflunomide in the core study, had MRI and clinical relapse assessments at months 12 (n = 552) and 18, and entered the extension. Patients were allocated risk scores for disability worsening (DW) after 1 year of teriflunomide treatment: 0 5 low risk; 1 5 intermediate risk; and 2-3 = high risk, based on the occurrence of relapses (0 to >= 2) and/or active (new and enlarging) T-2-weighted (T(2)w) lesions (<= 3 or >3) after the 1-year MRI. Patients in the intermediate-risk group were reclassified as responders or nonresponders (low or high risk) according to relapses and T(2)w lesions on the 18-month MRI. Long-term risk (7 years) of DW was assessed by Kaplan-Meier survival curves. Results: In patients with a score of 2-3, the risk of 12-week-confirmed DW over 7 years was significantly higher vs those with a score of 0 (hazard ratio [HR] = 1.96, p = 0.0044). Patients reclassified as high risk at month 18 (18.6%) had a significantly higher risk of DW vs those in the low-risk group (81.4%; HR = 1.92; p = 0.0004). Conclusions: Over 80% of patients receiving teriflunomide were classified as low risk (responders) and had a significantly lower risk of DW than those at increased risk (nonresponders) over 7 years of follow-up in TEMSO. Close monitoring of relapses and active T(2)w lesions after short-term teriflunomide treatment predicts a differential rate of subsequent DW long term.
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