| Literature DB >> 27215218 |
Woo-Jin Lee1,2, Soon-Tae Lee1,2, Jangsup Moon1,2, Jun-Sang Sunwoo1,2, Jung-Ick Byun1,2, Jung-Ah Lim1,2, Tae-Joon Kim1,2, Yong-Won Shin1,2, Keon-Joo Lee1,2, Jin-Sun Jun1,2, Han Sang Lee1,2, Soyun Kim1, Kyung-Il Park1,3, Keun-Hwa Jung1,2, Ki-Young Jung1,2, Manho Kim1,2, Sang Kun Lee4,5, Kon Chu6,7.
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.Entities:
Keywords: Autoimmune disorders; encephalitis; immunotherapy; prognosis; tocilizumab
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Year: 2016 PMID: 27215218 PMCID: PMC5081109 DOI: 10.1007/s13311-016-0442-6
Source DB: PubMed Journal: Neurotherapeutics ISSN: 1878-7479 Impact factor: 7.620