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July 10, 2018; 91 (2) Clinical/Scientific Notes

Autoimmune pancerebellitis associated with pembrolizumab therapy

Jeffrey R. Vitt, Collin Kreple, Nausheen Mahmood, Elliot Dickerson, Giselle Y. Lopez, Megan B. Richie
First published June 6, 2018, DOI: https://doi.org/10.1212/WNL.0000000000005781
Jeffrey R. Vitt
From the Department of Neurology (J.R.V., C.K., M.B.R.), School of Medicine (N.M.), Division of Neuroradiology, Department of Radiology (E.D.), and Division of Neuropathology, Department of Pathology (G.Y.L.), University of California San Francisco.
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Collin Kreple
From the Department of Neurology (J.R.V., C.K., M.B.R.), School of Medicine (N.M.), Division of Neuroradiology, Department of Radiology (E.D.), and Division of Neuropathology, Department of Pathology (G.Y.L.), University of California San Francisco.
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Nausheen Mahmood
From the Department of Neurology (J.R.V., C.K., M.B.R.), School of Medicine (N.M.), Division of Neuroradiology, Department of Radiology (E.D.), and Division of Neuropathology, Department of Pathology (G.Y.L.), University of California San Francisco.
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Elliot Dickerson
From the Department of Neurology (J.R.V., C.K., M.B.R.), School of Medicine (N.M.), Division of Neuroradiology, Department of Radiology (E.D.), and Division of Neuropathology, Department of Pathology (G.Y.L.), University of California San Francisco.
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Giselle Y. Lopez
From the Department of Neurology (J.R.V., C.K., M.B.R.), School of Medicine (N.M.), Division of Neuroradiology, Department of Radiology (E.D.), and Division of Neuropathology, Department of Pathology (G.Y.L.), University of California San Francisco.
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Megan B. Richie
From the Department of Neurology (J.R.V., C.K., M.B.R.), School of Medicine (N.M.), Division of Neuroradiology, Department of Radiology (E.D.), and Division of Neuropathology, Department of Pathology (G.Y.L.), University of California San Francisco.
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Citation
Autoimmune pancerebellitis associated with pembrolizumab therapy
Jeffrey R. Vitt, Collin Kreple, Nausheen Mahmood, Elliot Dickerson, Giselle Y. Lopez, Megan B. Richie
Neurology Jul 2018, 91 (2) 91-93; DOI: 10.1212/WNL.0000000000005781

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This article requires a subscription to view the full text. If you have a subscription you may use the login form below to view the article. Access to this article can also be purchased.

Checkpoint proteins reduce immune-mediated responses to promote self-tolerance and prevent autoimmunity. Programmed cell death protein 1 (PD-1) is a checkpoint receptor protein expressed on leukocytes that inactivates T cell–mediated immunity when bound to ligand PD-L1. Certain tumors can escape immune-mediated destruction by expressing high concentrations of PD-L1, evading host surveillance.1 PD-1 pathway inhibitors effectively treat multiple malignancies including melanoma, non-small cell lung cancer, and squamous cell carcinoma.2 However, there is increasing recognition of immune-related adverse events (irAE) associated with checkpoint inhibitor therapy due to dysregulated immune system activation.1 We report immune-mediated cerebellitis following pembrolizumab.

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  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Received November 13, 2017.
  • Accepted in final form March 22, 2018.
  • © 2018 American Academy of Neurology
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