TY - JOUR
T1 - Interleukin 6 receptor blockade in patients with neuromyelitis optica nonresponsive to anti-cd20 therapy
AU - Ayzenberg, Ilya
AU - Kleiter, Ingo
AU - Schröder, Alexandra
AU - Hellwig, Kerstin
AU - Chan, Andrew
AU - Yamamura, Takashi
AU - Gold, Ralf
PY - 2013/3
Y1 - 2013/3
N2 - Objective: To report first experiences with interleukin 6 receptor inhibition in therapy-resistant neuromyelitis optica (NMO). Design: Retrospective case series. Setting: Neurology department at a tertiary referral center. Patients: Patients with an aggressive course of NMO switched to tocilizumab after failure of anti-CD20 therapy. Main Outcome Measures: Annualized relapse rate and disability progression measured by the Expanded Disability Status Scale. Results: We report 3 female patients with a median age of 39 years (range, 26-40 years) and aquaporin 4-positive NMO. All patients had been treated with different immunosuppressive and immunomodulating agents, followed by 1 to 3 cycles of rituximab. Despite complete CD20-cell depletion during rituximab therapy, the median annualized relapse rate was 3.0 (range, 2.3-3.0) and the median Expanded Disability Status Scale score increased from 5.0 (range, 4.5-7.0) to 6.5 (range, 5.0- 7.0). After the switch to tocilizumab (median duration of therapy, 18 months), the median annualized relapse rate decreased to 0.6 (range, 0-1.3). A total of 2 relapses occurred; however, they were mild and there were no changes in clinical disability. Conclusions: Interleukin 6 receptor-blocking therapy can be effective in therapy-resistant cases of NMO. Larger controlled studies are needed to confirm the efficacy of tocilizumab.
AB - Objective: To report first experiences with interleukin 6 receptor inhibition in therapy-resistant neuromyelitis optica (NMO). Design: Retrospective case series. Setting: Neurology department at a tertiary referral center. Patients: Patients with an aggressive course of NMO switched to tocilizumab after failure of anti-CD20 therapy. Main Outcome Measures: Annualized relapse rate and disability progression measured by the Expanded Disability Status Scale. Results: We report 3 female patients with a median age of 39 years (range, 26-40 years) and aquaporin 4-positive NMO. All patients had been treated with different immunosuppressive and immunomodulating agents, followed by 1 to 3 cycles of rituximab. Despite complete CD20-cell depletion during rituximab therapy, the median annualized relapse rate was 3.0 (range, 2.3-3.0) and the median Expanded Disability Status Scale score increased from 5.0 (range, 4.5-7.0) to 6.5 (range, 5.0- 7.0). After the switch to tocilizumab (median duration of therapy, 18 months), the median annualized relapse rate decreased to 0.6 (range, 0-1.3). A total of 2 relapses occurred; however, they were mild and there were no changes in clinical disability. Conclusions: Interleukin 6 receptor-blocking therapy can be effective in therapy-resistant cases of NMO. Larger controlled studies are needed to confirm the efficacy of tocilizumab.
UR - http://www.scopus.com/inward/record.url?scp=84874904135&partnerID=8YFLogxK
U2 - 10.1001/jamaneurol.2013.1246
DO - 10.1001/jamaneurol.2013.1246
M3 - Article
AN - SCOPUS:84874904135
SN - 2168-6149
VL - 70
SP - 394
EP - 397
JO - JAMA Neurology
JF - JAMA Neurology
IS - 3
ER -