Title |
Tocilizumab in Autoimmune Encephalitis Refractory to Rituximab: An Institutional Cohort Study
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Published in |
Neurotherapeutics, October 2016
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DOI | 10.1007/s13311-016-0442-6 |
Pubmed ID | |
Authors |
Woo-Jin Lee, Soon-Tae Lee, Jangsup Moon, Jun-Sang Sunwoo, Jung-Ick Byun, Jung-Ah Lim, Tae-Joon Kim, Yong-Won Shin, Keon-Joo Lee, Jin-Sun Jun, Han Sang Lee, Soyun Kim, Kyung-Il Park, Keun-Hwa Jung, Ki-Young Jung, Manho Kim, Sang Kun Lee, Kon Chu |
Abstract |
A considerable portion of autoimmune encephalitis (AE) does not respond to conventional immunotherapies and subsequently has poor outcomes. We aimed to determine the efficacy of tocilizumab, an anti-interleukin-6 antibody, in rituximab-refractory AE compared with other treatment options. From an institutional cohort of AE, 91 patients with inadequate clinical response to first-line immunotherapy and following rituximab were retrospectively reviewed. Patients were grouped according to their further immunotherapy strategies. Thirty (33.0 %) patients were included in the tocilizumab group, 31 (34.0 %) in the additional rituximab group, and 30 (33.0 %) in the observation group. Outcomes were defined as the favorable modified Rankin Scale scores (≤2) at 1 and 2 months from the initiation of each treatment strategy and at the last follow-up. Favorable clinical response (improvement of the modified Rankin Scale scores by ≥ 2 points or achievement of the mRS scores ≤ 2) at the last follow-up was also analyzed. The tocilizumab group showed more frequent favorable mRS scores at 2 months from treatment initiation and at the last follow-up compared with those at the relevant time points of the remaining groups. The majority (89.5 %) of the patients with clinical improvement at 1 month from tocilizumab treatment maintained a long-term favorable clinical response. No serious adverse effects of rituximab or tocilizumab were reported. Therefore, we suggest that tocilizumab might be a good treatment strategy for treating AE refractory to conventional immunotherapies and rituximab. The tocilizumab-mediated clinical improvement manifests as early at 1 month after treatment initiation. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Spain | 1 | 17% |
United Kingdom | 1 | 17% |
Unknown | 4 | 67% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 4 | 67% |
Scientists | 1 | 17% |
Practitioners (doctors, other healthcare professionals) | 1 | 17% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 167 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Other | 23 | 14% |
Researcher | 18 | 11% |
Student > Bachelor | 16 | 10% |
Student > Postgraduate | 15 | 9% |
Student > Doctoral Student | 15 | 9% |
Other | 31 | 19% |
Unknown | 49 | 29% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 57 | 34% |
Neuroscience | 27 | 16% |
Pharmacology, Toxicology and Pharmaceutical Science | 4 | 2% |
Agricultural and Biological Sciences | 4 | 2% |
Psychology | 3 | 2% |
Other | 10 | 6% |
Unknown | 62 | 37% |