Association of Autoimmune Encephalitis With Combined Immune Checkpoint Inhibitor Treatment for Metastatic Cancer

被引:216
作者
Williams, Tanya J. [1 ]
Benavides, David R. [1 ]
Patrice, Kelly-Ann [1 ]
Dalmau, Josep O. [2 ,3 ]
de Avila, Alexandre Leon Ribeiro [4 ]
Le, Dung T. [5 ]
Lipson, Evan J. [5 ]
Probasco, John C. [1 ]
Mowry, Ellen M. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, 600 N Wolfe St,Pathol Bldg,Ste 627, Baltimore, MD 21287 USA
[2] Univ Barcelona, Inst Invest Biomed August Pi & Sunyer, Hosp Clin, Dept Neurol, Barcelona, Spain
[3] Univ Barcelona, Inst Catalana Recerca & Estudis Avancats, Barcelona, Spain
[4] Bristol Myers Squibb, Plainsboro, NJ USA
[5] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
NMDA-RECEPTOR ENCEPHALITIS; MALIGNANT-MELANOMA; IPILIMUMAB THERAPY; LUNG-CANCER; ANTIBODIES; ENCEPHALOPATHY; SAFETY; GRIN2A;
D O I
10.1001/jamaneurol.2016.1399
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IMPORTANCE Paraneoplastic encephalitides usually precede a diagnosis of cancer and are often refractory to immunosuppressive therapy. Conversely, autoimmune encephalitides are reversible conditions that can occur in the presence or absence of cancer. OBJECTIVE To report the induction of autoimmune encephalitis in 2 patients after treatment of metastatic cancer with a combination of the immune checkpoint inhibitors nivolumab and ipilimumab. DESIGN, SETTING, AND PARTICIPANTS A retrospective case study was conducted of the clinical and management course of 2 patients with progressive, treatment-refractory metastatic cancer who were treated with a single dose each (concomitantly) of the immune checkpoint inhibitors nivolumab, 1 mg/kg, and ipilimumab, 3 mg/kg. EXPOSURES Nivolumab and ipilimumab. MAIN OUTCOMES AND MEASURES The clinical response to immunosuppressive therapy in suspected autoimmune encephalitis in the setting of immune checkpoint inhibitor use. RESULTS Autoantibody testing confirmed identification of anti-N-methyl-D-aspartate receptor antibodies in the cerebrospinal fluid of 1 patient. Withdrawal of immune checkpoint inhibitors and initiation of immunosuppressive therapy, consisting of intravenous methylprednisolone sodium succinate equivalent to 1000 mg of methylprednisolone for 5 days, 0.4 mg/kg/d of intravenous immunoglobulin for 5 days, and 2 doses of rituximab, 1000 mg, in 1 patient and oral prednisone, 60 mg/d, in the other patient, resulted in improved neurologic symptoms. CONCLUSIONS AND RELEVANCE Immune checkpoint inhibition may favor the development of immune responses against neuronal antigens, leading to autoimmune encephalitis. Early recognition and treatment of autoimmune encephalitis in patients receiving immune checkpoint blockade therapy will likely be essential for maximizing clinical recovery and minimizing the effect of drug-related toxic effects. The mechanisms by which immune checkpoint inhibition may contribute to autoimmune encephalitis require further study.
引用
收藏
页码:928 / 933
页数:6
相关论文
共 28 条
[1]   Severe meningo-radiculo-nevritis associated with ipilimumab [J].
Bompaire, Flavie ;
Mateus, Christine ;
Taillia, Herve ;
De Greslan, Thierry ;
Lahutte, Marion ;
Sallansonnet-Froment, Magali ;
Ouologuem, Madani ;
Renard, Jean-Luc ;
Gorochov, Guy ;
Robert, Caroline ;
Ricard, Damien .
INVESTIGATIONAL NEW DRUGS, 2012, 30 (06) :2407-2410
[2]  
Bot Ilja, 2013, Pract Neurol, V13, P278, DOI 10.1136/practneurol-2012-000447
[3]  
Boyd K, 2015, IMMUNOME RES, V11, DOI DOI 10.4172/1745-7580.1000092
[4]   Phase I Study of Single-Agent Anti-Programmed Death-1 (MDX-1106) in Refractory Solid Tumors: Safety, Clinical Activity, Pharmacodynamics, and Immunologic Correlates [J].
Brahmer, Julie R. ;
Drake, Charles G. ;
Wollner, Ira ;
Powderly, John D. ;
Picus, Joel ;
Sharfman, William H. ;
Stankevich, Elizabeth ;
Pons, Alice ;
Salay, Theresa M. ;
McMiller, Tracee L. ;
Gilson, Marta M. ;
Wang, Changyu ;
Selby, Mark ;
Taube, Janis M. ;
Anders, Robert ;
Chen, Lieping ;
Korman, Alan J. ;
Pardoll, Drew M. ;
Lowy, Israel ;
Topalian, Suzanne L. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (19) :3167-3175
[5]   CTLA-4 blockade with ipilimumab: biology, safety, efficacy, and future considerations [J].
Camacho, Luis H. .
CANCER MEDICINE, 2015, 4 (05) :661-672
[6]   Ipilimumab-Induced Encephalopathy with a Reversible Splenial Lesion [J].
Conry, Robert M. ;
Sullivan, Joseph C. ;
Nabors, Louis B., III .
CANCER IMMUNOLOGY RESEARCH, 2015, 3 (06) :598-601
[7]   Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis [J].
Dalmau, Josep ;
Lancaster, Eric ;
Martinez-Hernandez, Eugenia ;
Rosenfeld, Myrna R. ;
Balice-Gordon, Rita .
LANCET NEUROLOGY, 2011, 10 (01) :63-74
[8]   Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies [J].
Dalmau, Josep ;
Gleichman, Amy J. ;
Hughes, Ethen G. ;
Rossi, Jeffrey E. ;
Peng, Xiaoyu ;
Lai, Meizan ;
Dessain, Scott K. ;
Rosenfeld, Mynna R. ;
Balice-Gordon, Rita ;
Lynch, David R. .
LANCET NEUROLOGY, 2008, 7 (12) :1091-1098
[9]   Paraneoplastic syndromes involving the nervous system [J].
Darnell, RB ;
Posner, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (16) :1543-1554
[10]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247