Neurological autoimmunity in melanoma patients: a comparison between those exposed and non-exposed to immune checkpoint inhibitors.

Autoimmune diseases of the nervous system Immunotherapy Nervous system Neurologic immune-related adverse event (n-irAE) Oncology Paraneoplastic syndromes

Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
11 Mar 2024
Historique:
received: 29 11 2023
accepted: 10 02 2024
revised: 09 02 2024
medline: 12 3 2024
pubmed: 12 3 2024
entrez: 12 3 2024
Statut: aheadofprint

Résumé

The clinical spectrum of melanoma-associated neurological autoimmunity, whether melanoma-associated paraneoplastic neurological syndromes (PNS) or induced by immune checkpoint inhibitors (ICI), is not well characterized. We aim to describe the clinical spectrum of melanoma-associated neurological autoimmunity. A systematic review of the literature combined with patients from French databases of paraneoplastic neurological syndromes was conducted. All melanoma patients with a possible immune-mediated neurologic syndrome were included and classified according to whether they had previously been exposed to ICI (ICI-neurotoxicity) or not (ICI-naïve) at first neurological symptoms. Seventy ICI-naïve (literature: n = 61) and 241 ICI-neurotoxicity patients (literature: n = 180) were identified. Neuromuscular manifestations predominated in both groups, but peripheral neuropathies were more frequent in ICI-neurotoxicity patients (39.4% vs 21.4%, p = 0.005) whereas myositis was more frequent in ICI-naïve patients (42.9% vs 18.7%, p < 0.001). ICI-naïve patients had also more frequent central nervous system (CNS) involvement (35.7% vs 23.7%, p = 0.045), classical paraneoplastic syndrome (25.7% vs 5.8%, p < 0.001), and more frequently positive for anti-neuron antibodies (24/32, 75.0% vs 38/90, 42.2%, p = 0.001). Although more ICI-neurotoxicity patients died during the acute phase (22/202, 10.9% vs 1/51, 2.0%, p = 0.047), mostly myositis patients (14/22, 63.6%), mortality during follow-up was higher in ICI-naïve patients (58.5% vs 29.8%, p < 0.001). There was no significant difference in the frequency of life independence (mRS ≤ 2) in the surviving patients in both groups (95.5% vs 91.0%, p = 0.437). Melanoma-associated PNS appear remarkably rare. The clinical similarities observed in neurological autoimmunity between ICI-treated and ICI-naïve patients, characterized predominantly by demyelinating polyradiculoneuropathy and myositis, suggest a potential prior immunization against melanoma antigens contributing to ICI-related neurotoxicity.

Sections du résumé

BACKGROUND BACKGROUND
The clinical spectrum of melanoma-associated neurological autoimmunity, whether melanoma-associated paraneoplastic neurological syndromes (PNS) or induced by immune checkpoint inhibitors (ICI), is not well characterized. We aim to describe the clinical spectrum of melanoma-associated neurological autoimmunity.
METHODS METHODS
A systematic review of the literature combined with patients from French databases of paraneoplastic neurological syndromes was conducted. All melanoma patients with a possible immune-mediated neurologic syndrome were included and classified according to whether they had previously been exposed to ICI (ICI-neurotoxicity) or not (ICI-naïve) at first neurological symptoms.
RESULTS RESULTS
Seventy ICI-naïve (literature: n = 61) and 241 ICI-neurotoxicity patients (literature: n = 180) were identified. Neuromuscular manifestations predominated in both groups, but peripheral neuropathies were more frequent in ICI-neurotoxicity patients (39.4% vs 21.4%, p = 0.005) whereas myositis was more frequent in ICI-naïve patients (42.9% vs 18.7%, p < 0.001). ICI-naïve patients had also more frequent central nervous system (CNS) involvement (35.7% vs 23.7%, p = 0.045), classical paraneoplastic syndrome (25.7% vs 5.8%, p < 0.001), and more frequently positive for anti-neuron antibodies (24/32, 75.0% vs 38/90, 42.2%, p = 0.001). Although more ICI-neurotoxicity patients died during the acute phase (22/202, 10.9% vs 1/51, 2.0%, p = 0.047), mostly myositis patients (14/22, 63.6%), mortality during follow-up was higher in ICI-naïve patients (58.5% vs 29.8%, p < 0.001). There was no significant difference in the frequency of life independence (mRS ≤ 2) in the surviving patients in both groups (95.5% vs 91.0%, p = 0.437).
CONCLUSIONS CONCLUSIONS
Melanoma-associated PNS appear remarkably rare. The clinical similarities observed in neurological autoimmunity between ICI-treated and ICI-naïve patients, characterized predominantly by demyelinating polyradiculoneuropathy and myositis, suggest a potential prior immunization against melanoma antigens contributing to ICI-related neurotoxicity.

Identifiants

pubmed: 38467790
doi: 10.1007/s00415-024-12252-0
pii: 10.1007/s00415-024-12252-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Agence Nationale de la Recherche
ID : ANR-18-RHUS-0012

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

Références

Greenlee JE, Carlson NG, Abbatemarco JR et al (2022) Paraneoplastic and other autoimmune encephalitides: antineuronal antibodies, T lymphocytes, and questions of pathogenesis. Front Neurol 12:1–16. https://doi.org/10.3389/fneur.2021.744653
doi: 10.3389/fneur.2021.744653
Yeh I, Bastian BC (2021) Melanoma pathology: new approaches and classification. Br J Dermatol. https://doi.org/10.1111/bjd.20427
doi: 10.1111/bjd.20427 pubmed: 34060071 pmcid: 9292921
Elder DE, Bastian BC, Cree IA et al (2020) The 2018 World Health Organization classification of cutaneous, mucosal, and uveal melanoma detailed analysis of 9 distinct subtypes defined by their evolutionary pathway. Arch Pathol Lab Med 144:500–522. https://doi.org/10.5858/arpa.2019-0561-RA
doi: 10.5858/arpa.2019-0561-RA pubmed: 32057276
Ko JS (2017) The immunology of melanoma. Clin Lab Med 37:449–471. https://doi.org/10.1016/j.cll.2017.06.001
doi: 10.1016/j.cll.2017.06.001 pubmed: 28802495
Koebel CM, Vermi W, Swann JB et al (2007) Adaptive immunity maintains occult cancer in an equilibrium state. Nature 450:903–907. https://doi.org/10.1038/nature06309
doi: 10.1038/nature06309 pubmed: 18026089
Vesely MD, Kershaw MH, Schreiber RD et al (2011) Natural innate and adaptive immunity. Annu Rev Immunol 235–71:235–271
doi: 10.1146/annurev-immunol-031210-101324
Vilaseca A, Martínez-Sáez E, González V et al (2023) Teaching neuroimage: paraneoplastic cerebellar degeneration and antibodies to TRIM 9 and 67 secondary to melanoma. Neurology 101:e1652–e1653. https://doi.org/10.1212/WNL.0000000000207702
doi: 10.1212/WNL.0000000000207702 pubmed: 37580164
Bataller L, Sabater L, Saiz A et al (2004) Carbonic anhydrase-related protein VIII: autoantigen in paraneoplastic cerebellar degeneration. Ann Neurol 56:575–579. https://doi.org/10.1002/ana.20238
doi: 10.1002/ana.20238 pubmed: 15389893
Dalmau J, Graus F (2022) Autoimmune encephalitis and related disorders of the nervous system, 1st ed. Cambridge University Press. https://doi.org/10.1017/9781108696722
doi: 10.1017/9781108696722
Antoine J-C, Camdessanche J-P (2004) Paraneoplastic peripheral neuropathies. Rev Neurol (Paris) 160:188–198. https://doi.org/10.1016/s0035-3787(04)70890-5
doi: 10.1016/s0035-3787(04)70890-5 pubmed: 15034476
Kloos L, Sillevis Smitt P, Ang CW et al (2003) Paraneoplastic ophthalmoplegia and subacute motor axonal neuropathy associated with anti-GQ1b antibodies in a patient with malignant melanoma. J Neurol Neurosurg Psychiatry 74:507–509. https://doi.org/10.1136/jnnp.74.4.507
doi: 10.1136/jnnp.74.4.507 pubmed: 12640075 pmcid: 1738398
Nicolae CD, Nicolae I (2013) Antibodies against GM1 gangliosides associated with metastatic melanoma. Acta Dermatovenerol Croat 21:86–92
pubmed: 24001415
Graus F, Vogrig A, Muñiz-Castrillo S et al (2021) Updated diagnostic criteria for paraneoplastic neurologic syndromes. Neurol Neuroimmunol Neuroinflam 8:e1014–e1027. https://doi.org/10.1212/NXI.0000000000001014
doi: 10.1212/NXI.0000000000001014
Rosenfeld MR, Dalmau J (2018) Paraneoplastic neurologic syndromes. Neurol Clin 36:675–685. https://doi.org/10.1016/j.ncl.2018.04.015
doi: 10.1016/j.ncl.2018.04.015 pubmed: 30072076
Taliansky A, Furman O, Gadot M et al (2021) Immune checkpoint inhibitors-related encephalitis in melanoma and non-melanoma cancer patients: a single center experience. Support Care Cancer 29:7563–7568. https://doi.org/10.1007/s00520-021-06331-5
doi: 10.1007/s00520-021-06331-5 pubmed: 34120259 pmcid: 8550117
Marini A, Bernardini A, Gigli GL et al (2021) Neurologic adverse events of immune checkpoint inhibitors: a systematic review. Neurology 96:754–766. https://doi.org/10.1212/WNL.0000000000011795
doi: 10.1212/WNL.0000000000011795 pubmed: 33653902
Pepys J, Stoff R, Ramon-Gonen R et al (2023) Incidence and outcome of neurologic immune-related adverse events associated with immune checkpoint inhibitors in patients with melanoma. Neurology. https://doi.org/10.1212/WNL.0000000000207632
doi: 10.1212/WNL.0000000000207632 pubmed: 37652699
Guidon AC, Burton LB, Chwalisz BK et al (2021) Consensus disease definitions for neurologic immune-related adverse events of immune checkpoint inhibitors. J Immunother cancer. https://doi.org/10.1136/jitc-2021-002890
doi: 10.1136/jitc-2021-002890 pubmed: 34544895 pmcid: 8454442
Wang M, Rajan SS, Jacob AP et al (2020) Retrospective collection of 90-day modified Rankin Scale is accurate. Clin Trials 17:637–643. https://doi.org/10.1177/1740774520942466
doi: 10.1177/1740774520942466 pubmed: 32755236
Graus F, Titulaer MJ, Balu R et al (2016) A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol 15:391–404. https://doi.org/10.1016/S1474-4422(15)00401-9
doi: 10.1016/S1474-4422(15)00401-9 pubmed: 26906964 pmcid: 5066574
Van den Bergh PYK, Hadden RDM, Bouche P et al (2010) European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Periphe. Eur J Neurol 17:356–363. https://doi.org/10.1111/j.1468-1331.2009.02930.x
doi: 10.1111/j.1468-1331.2009.02930.x pubmed: 20456730
Asbury AK, Cornblath DR (1990) Assessment of current diagnostic criteria for Guillain-Barré syndrome. Ann Neurol 27(Suppl):S21–S24. https://doi.org/10.1002/ana.410270707
doi: 10.1002/ana.410270707 pubmed: 2194422
Van den Bergh PYK, van Doorn PA, Hadden RDM et al (2021) European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint Task Force-Second revision. Eur J Neurol 28:3556–3583. https://doi.org/10.1111/ene.14959
doi: 10.1111/ene.14959 pubmed: 34327760
Huang J, Chan SC, Ko S et al (2023) Global incidence, mortality, risk factors and trends of melanoma: a systematic analysis of registries. Am J Clin Dermatol. https://doi.org/10.1007/s40257-023-00795-3
doi: 10.1007/s40257-023-00795-3 pubmed: 37296344
Filippi L, Bianconi F, Schillaci O, Angela Spanu BP (2022) The role and potential of 18 F-FDG PET/CT in malignant melanoma : prognostication, monitoring response to targeted. Diagnostics. https://doi.org/10.3390/diagnostics12040929
doi: 10.3390/diagnostics12040929 pubmed: 36292114 pmcid: 9601187
Moghadam-Kia S, Oddis CV, Ascherman DP, Aggarwal R (2020) Risk factors and cancer screening in myositis. Rheum Dis Clin North Am 46:565–576. https://doi.org/10.1016/j.rdc.2020.05.006
doi: 10.1016/j.rdc.2020.05.006 pubmed: 32631604
Rajabally YA, Attarian S (2018) Chronic inflammatory demyelinating polyneuropathy and malignancy: a systematic review. Muscle Nerve 57:875–883. https://doi.org/10.1002/mus.26028
doi: 10.1002/mus.26028 pubmed: 29194677
Villagrán-García M, Muñiz-Castrillo S, Ciano-Petersen NL et al (2023) Paraneoplastic neurological syndromes associated with renal or bladder cancer: case series and PRISMA-IPD systematic review. J Neurol 270:283–299. https://doi.org/10.1007/s00415-022-11356-9
doi: 10.1007/s00415-022-11356-9 pubmed: 36050418
Tsuchida T, Saxton RE, Morton DLIR (1989) Gangliosides of human melanoma. Cancer 63:1166–1174
doi: 10.1002/1097-0142(19890315)63:6<1166::AID-CNCR2820630621>3.0.CO;2-5 pubmed: 2917320
Weiss MD, Luciano CA, Dalakas MC, Quarles RH (1998) Molecular mimicry in chronic inflammatory demyelinating polyneuropathy and melanoma. Neurology 51:1738–1741
doi: 10.1212/WNL.51.6.1738 pubmed: 9855537
Farina A, Birzu C, Elsensohn M et al (2023) Neurological outcomes in immune checkpoint inhibitor-related neurotoxicity. Brain Commun. https://doi.org/10.1093/braincomms/fcad186
doi: 10.1093/braincomms/fcad186 pubmed: 37794924 pmcid: 10546956
Poujade L, Samaran Q, Mura F et al (2021) Melanoma-associated retinopathy during pembrolizumab treatment probably controlled by intravitreal injections of dexamethasone. Doc Ophthalmol 142:257–263. https://doi.org/10.1007/s10633-020-09795-8
doi: 10.1007/s10633-020-09795-8 pubmed: 32975694
Sechi E, Markovic SN, McKeon A et al (2020) Neurologic autoimmunity and immune checkpoint inhibitors: autoantibody profiles and outcomes. Neurology 95:e2442–e2452. https://doi.org/10.1212/WNL.0000000000010632
doi: 10.1212/WNL.0000000000010632 pubmed: 32796130 pmcid: 7682911
Elsheikh S, Gurney SP, Burdon MA (2020) Melanoma-associated retinopathy. Clin Exp Dermatol 45:147–152. https://doi.org/10.1111/ced.14095
doi: 10.1111/ced.14095 pubmed: 31742740
Bourke JM, O’Sullivan M, Khattak MA (2016) Management of adverse events related to new cancer immunotherapy (immune checkpoint inhibitors). Med J Aust 205:418–424. https://doi.org/10.5694/mja16.00586
doi: 10.5694/mja16.00586 pubmed: 27809739
Castanares-Zapatero D, Verleye L, Devos C et al (2024) Survival of patients with unfavorable prognosis cutaneous melanoma with increased use of immunotherapy agents: a population-based study in Belgium. Int J Dermatol. https://doi.org/10.1111/ijd.17046
doi: 10.1111/ijd.17046 pubmed: 38297428

Auteurs

Andreu Vilaseca (A)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Neurology Department.and Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.

Antonio Farina (A)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Macarena Villagrán-García (M)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Antoine Pegat (A)

Service ENMG et de Pathologies Neuromusculaires, Centre de Référence des Maladies Neuromusculaires PACA-Réunion-Rhône Alpes, Hôpital Neurologique P. Wertheimer, Hospices Civils de Lyon, Lyon, France.

Marie Benaiteau (M)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Nicolás Lundahl Ciano-Petersen (NL)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Le-Duy Do (LD)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Véronique Rogemond (V)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

David Gonçalves (D)

Service d'Anatomie Pathologique, Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, UMR CNRS Université de Lyon 1, Lyon, France.

Dimitri Psimaras (D)

Service de Neurologie 2- Mazarin, Sorbonne Université, Inserm, CNRS, UMR S 1127, Institut du Cerveau, ICM, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière - Charles Foix, , 75013, Paris, France.
OncoNeuroTox Group, Center for Patients with Neurological Complications of Oncologic Treatments, GH Pitié-Salpetrière et Hôpital Percy, Paris, France.

Cristina Birzu (C)

Service de Neurologie 2- Mazarin, Sorbonne Université, Inserm, CNRS, UMR S 1127, Institut du Cerveau, ICM, AP-HP, Hôpitaux Universitaires La Pitié Salpêtrière - Charles Foix, , 75013, Paris, France.
OncoNeuroTox Group, Center for Patients with Neurological Complications of Oncologic Treatments, GH Pitié-Salpetrière et Hôpital Percy, Paris, France.

Jérôme Honnorat (J)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Bastien Joubert (B)

French Reference Center on Paraneoplastic Neurological Syndromes and Autoimmune Encephalitis, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France. bastien.joubert@chu-lyon.fr.
MeLiS - UCBL - CNRS UMR 5284 - INSERM U1314, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France. bastien.joubert@chu-lyon.fr.
ImmuCare, Institute of Cancerology, Hospices Civils de Lyon, Lyon, France. bastien.joubert@chu-lyon.fr.
Service de Neurologie, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Lyon, France. bastien.joubert@chu-lyon.fr.
Centre de Référence National pour les Syndromes Neurologiques Paranéoplasiques, Hôpital Neurologique, 59 Boulevard Pinel, 69677, Bron Cedex, France. bastien.joubert@chu-lyon.fr.

Classifications MeSH