Efficacy of immunotherapy and prognosis in anti-LGI1 encephalitis patients: A meta-analysis

Ann Clin Transl Neurol. 2023 Sep;10(9):1578-1589. doi: 10.1002/acn3.51847. Epub 2023 Jul 13.

Abstract

Objective: To assess the efficacy and safety of immunotherapy for LGI1 antibody encephalitis, and consider the predictors of poor outcomes following immunotherapy.

Methods: We searched PubMed and Embase for articles reporting the immunotherapy data of anti-LGI1 encephalitis patients. The proportions of patients with poor outcomes (modified Rankin Scale [mRS] score > 2) at 3 months, 12 months, and the last follow-up, as well as the odds ratio [OR] of predictors were pooled.

Results: The review included 162 articles with 1066 patients. The proportion of patients with poor functional outcomes was 21% at 3 months, 14% at 12 months, and 14% at the last follow-up after receiving immunotherapy. The proportion of patients with reported relapse was 16.6%. The mean duration from onset to the first relapse was 15.6 months. Predictors significantly associated with poor outcomes were age (increase of 1 year), the presence of cognitive impairment, and CSF LGI1 antibody positive. We did not find a statistically significant association between the worst mRS score in the acute phase, the presence of faciobrachial dystonic seizures (FBDS), days from symptom onset to immunotherapy, second-line treatment, maintenance immunotherapy, or follow-up time and outcomes.

Interpretation: Although most patients respond to immunotherapy, a minority of patients still have poor outcomes. Advanced age, cognitive impairment, and CSF LGI1 antibody positive are associated with an increased risk of poor outcomes. However, due to the insufficiency of the data, these conclusions need to be interpreted with caution.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Encephalitis* / therapy
  • Humans
  • Immunotherapy / adverse effects
  • Intracellular Signaling Peptides and Proteins
  • Limbic Encephalitis*
  • Neoplasm Recurrence, Local
  • Prognosis

Substances

  • Intracellular Signaling Peptides and Proteins

Grants and funding

This work was funded by The National Key R&D Program of China grant 2022YFC2503800; The National Science Foundation of China grant 81971213.