TY - JOUR
T1 - Risk of requiring a wheelchair in primary progressive multiple sclerosis
T2 - Data from the ORATORIO trial and the MSBase registry
AU - Butzkueven, Helmut
AU - Spelman, Tim
AU - Horakova, Dana
AU - Hughes, Stella
AU - Solaro, Claudio
AU - Izquierdo, Guillermo
AU - Kubala Havrdová, Eva
AU - Grand'Maison, Francois
AU - Prat, Alexandre
AU - Girard, Marc
AU - Hupperts, Raymond
AU - Onofrj, Marco
AU - Lugaresi, Alessandra
AU - Taylor, Bruce
AU - Giovannoni, Gavin
AU - Kappos, Ludwig
AU - Hauser, Stephen L.
AU - Montalban, Xavier
AU - Craveiro, Licinio
AU - Freitas, Rita
AU - Model, Fabian
AU - Overell, James
AU - Muros-Le Rouzic, Erwan
AU - Sauter, Annette
AU - Wang, Qing
AU - Wormser, David
AU - Wolinsky, Jerry S.
N1 - Publisher Copyright:
© 2021 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology
PY - 2022/4
Y1 - 2022/4
N2 - Background and purpose: Reaching Expanded Disability Status Scale (EDSS) ≥7.0 represents the requirement for a wheelchair. Here we (i) assess the effect of ocrelizumab on time to EDSS ≥7.0 over the ORATORIO (NCT01194570) double-blind and extended controlled periods (DBP+ECP), (ii) quantify likely long-term benefits by extrapolating results, and (iii) assess the plausibility of extrapolations using an independent real-world cohort (MSBase registry; ACTRN12605000455662). Methods: Post hoc analyses assessing time to 24-week confirmed EDSS ≥7.0 in two cohorts of patients with primary progressive multiple sclerosis (baseline EDSS 3.0–6.5) were investigated in ORATORIO and MSBase. Results: In the ORATORIO DBP+ECP, ocrelizumab reduced the risk of 24-week confirmed EDSS ≥7.0 (hazard ratio = 0.54, 95% confidence interval [CI]: 0.31–0.92; p = 0.022). Extrapolated median time to 24-week confirmed EDSS ≥7.0 was 12.1 and 19.2 years for placebo and ocrelizumab, respectively (7.1-year delay [95% CI: −4.3 to 18.4]). In MSBase, the median time to 24-week confirmed EDSS ≥7.0 was 12.4 years. Conclusions: Compared with placebo, ocrelizumab significantly delayed time to 24-week confirmed wheelchair requirement in ORATORIO. The plausibility of the extrapolated median time to reach this milestone in the placebo group was supported by observed real-world data from MSBase. Extrapolated benefits for ocrelizumab over placebo could represent a truly meaningful delay in loss of ambulation and independence.
AB - Background and purpose: Reaching Expanded Disability Status Scale (EDSS) ≥7.0 represents the requirement for a wheelchair. Here we (i) assess the effect of ocrelizumab on time to EDSS ≥7.0 over the ORATORIO (NCT01194570) double-blind and extended controlled periods (DBP+ECP), (ii) quantify likely long-term benefits by extrapolating results, and (iii) assess the plausibility of extrapolations using an independent real-world cohort (MSBase registry; ACTRN12605000455662). Methods: Post hoc analyses assessing time to 24-week confirmed EDSS ≥7.0 in two cohorts of patients with primary progressive multiple sclerosis (baseline EDSS 3.0–6.5) were investigated in ORATORIO and MSBase. Results: In the ORATORIO DBP+ECP, ocrelizumab reduced the risk of 24-week confirmed EDSS ≥7.0 (hazard ratio = 0.54, 95% confidence interval [CI]: 0.31–0.92; p = 0.022). Extrapolated median time to 24-week confirmed EDSS ≥7.0 was 12.1 and 19.2 years for placebo and ocrelizumab, respectively (7.1-year delay [95% CI: −4.3 to 18.4]). In MSBase, the median time to 24-week confirmed EDSS ≥7.0 was 12.4 years. Conclusions: Compared with placebo, ocrelizumab significantly delayed time to 24-week confirmed wheelchair requirement in ORATORIO. The plausibility of the extrapolated median time to reach this milestone in the placebo group was supported by observed real-world data from MSBase. Extrapolated benefits for ocrelizumab over placebo could represent a truly meaningful delay in loss of ambulation and independence.
KW - disease progression
KW - ocrelizumab
KW - primary progressive multiple sclerosis
KW - wheelchair
UR - http://www.scopus.com/inward/record.url?scp=85105017493&partnerID=8YFLogxK
U2 - 10.1111/ene.14824
DO - 10.1111/ene.14824
M3 - Article
C2 - 33724638
AN - SCOPUS:85105017493
SN - 1351-5101
VL - 29
SP - 1082
EP - 1090
JO - European Journal of Neurology
JF - European Journal of Neurology
IS - 4
ER -