Abstract

Paraneoplastic neurological syndromes are more commonly seen with malignancies such as small cell lung cancer, thymoma, gynecological malignancies, and breast cancer as well as seminoma. With the introduction of immune checkpoint inhibitor (ICI) cancer immunotherapy we see an increase of autoimmune neurological complications in patients with malignancies not traditionally associated with paraneoplastic neurological syndromes, such as melanoma and renal cell carcinoma. Immune checkpoint inhibitors enhance antitumor immune responses resulting often in immune-related adverse effects that can affect any organ, including the central and peripheral nervous system, neuromuscular junction and muscle. Neurological complications are rare; neuromuscular complications are more common than central nervous system ones but multifocal neurological presentations are often encountered. The vast majority of neurological complications appear within 3 months of ICI initiation, but have been described even after ICI cessation. Neural autoantibody testing reveals autoantibodies in approximately half of the patients with CNS complications. Early suspicion and diagnosis is critical to avoid worsening and improve outcomes. Therapeutic strategies depend on the severity of the symptoms and initially typically involve discontinuation of ICI and high dose steroids. Further immunosuppression might be necessary. Outcomes are dependent on patient's characteristics and clinical presentations.

Highlights

  • The introduction of immune checkpoint inhibitors (ICI) has revolutionized the treatment of various malignancies

  • Guidelines for the treatment of immune related adverse events (irAE) according to the organ involved and the toxicity grade have been issued by the American Society of Clinical Oncology [82], the Society for Immunotherapy of Cancer Toxicity Management Working Group [21], and more recently the National Comprehensive Cancer Network (NCCN) [54]

  • Clinicians must be aware of the diverse spectrum of neurological toxicities associated with cancer immunotherapy

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Summary

INTRODUCTION

The introduction of immune checkpoint inhibitors (ICI) has revolutionized the treatment of various malignancies. Since ipilimumab was approved in 2011 for the treatment of metastatic melanoma, multiple new agents have been approved and the tumor indications have expanded, including non-small cell lung carcinoma (NSCLC), renal cell carcinoma, advanced Hodgkin lymphoma, urothelial carcinoma, small-cell lung cancer (SCLC) and Merkel cell carcinoma, amongst others [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20] These novel cancer immunotherapies enhance antitumor immune responses by blocking signaling pathways that have inhibitory effects on T-cell activation. We review the pathogenic mechanisms, clinical presentation, diagnostic approach, and therapeutic management of these complications

ICI MECHANISM OF ACTION
OF NEUROLOGICAL irAEs
Paraneoplastic Disorders Triggered by Immune Checkpoint Inhibitors
Clinical Syndromes
Diagnostic Findings in Patients With CNS
AND WHAT TO DO
GENERAL RECOMMENDATIONS FOR TREATMENT
Acute Treatment
Autoimmunity and Paraneoplastic
CONCLUSION
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