Abstract
Immune checkpoint inhibitor (ICI) therapy has revolutionized the management of various cancers with previously poor prognosis. Despite its great efficacy, the therapy is associated with a wide spectrum of immune-related adverse events (irAE) including neurological symptoms which can affect all parts of the central and peripheral nervous system. Even though these events are rare, they are of high relevance as the rate of residual symptoms or even fatal outcomes is remarkable. To provide a detailed overview of neurological adverse events associated with immune checkpoint-inhibitor therapy we conducted a literature search. While focusing on ipilimumab, nivolumab, and pembrolizumab therapy, all available case reports as well as larger case series and clinical trials have been considered. Eighty-two case reports about checkpoint-inhibitor therapy induced symptoms of the peripheral nervous system have been published, while only 43 case reports addressed central nervous system abnormalities. The frequency of immune checkpoint-inhibitor therapy inducing neurological adverse events is about 1% in larger studies. Especially neuromuscular adverse events exhibit distinct clinical and diagnostic characteristics. Additionally, several affected patients presented with overlap-syndromes, which means that symptoms and diagnostic findings indicating myositis, myasthenia gravis, and neuropathy were present in one individual patient at the same time. Thus, neurological and particularly neuromuscular adverse events of immune checkpoint-inhibitor therapy may constitute a new disease entity.
Highlights
The idea of targeting immune cells instead of cancer cells has led to a paradigm shift in oncology
Nivolumab-treated patients were affected more often compared with patients who received ipilimumab or pembrolizumab (7% vs. 1% and 2%) and combination therapy harboured the highest risk for development of Neurological adverse events (nAEs) (14%) [31]
We provide an overview of published case reports regarding nAEs of the central and peripheral nervous system published up to June 2019
Summary
The idea of targeting immune cells instead of cancer cells has led to a paradigm shift in oncology. Adverse events due to immune checkpoint blockade are frequent and will occur in up to 90% of anti-CTLA-4-antibody treated patients [3] and in about 70% of patients under treatment with anti-PD-1/anti-PD-L1 antibodies [4,5]. Besides endocrine dysfunction the skin and the digestive tract are the most affected organs regarding immune checkpoint-inhibitor (ICI) treatment associated irAEs [7,8]. Even though the risk to develop colitis, pneumonitis, and hepatitis was higher compared with standard treatment, the overall incidence for irAEs in this specific clinical trial was surprisingly low. IrAE rates are higher in patients treated with CTLA-4 antibodies than with PD-1 blockade [28]. The following sections will demonstrate that this does not apply for nAEs
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