Metastatic Merkel cell carcinoma and myasthenia gravis: contraindication for therapy with immune checkpoint inhibitors?


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
29 05 2019
Historique:
received: 29 01 2019
accepted: 17 05 2019
entrez: 31 5 2019
pubmed: 31 5 2019
medline: 28 5 2020
Statut: epublish

Résumé

PD-1/PD-L1 inhibitors are promising approaches for advanced Merkel cell carcinoma (MCC). Nevertheless, these inhibitors bear a high risk for induction of immune-related adverse events (irAEs), particularly flares of preexisting autoimmune diseases. Neurological irAEs of PD-1/PD-L1 inhibitors are possibly underestimated and potentially fatal toxicities. Additionally, exacerbations of preexisting myasthenia gravis (MG) with a high MG-specific-related mortality have been reported. A 61-year-old woman with a history of MG since 2005 was treated with azathioprine and pyridostigmine after thymectomy. In March 2016, she was diagnosed with MCC. Six months later the tumor had progressed to stage IV and metastases were detected in lymph nodes and the pancreas. The immunosuppressive therapy was therefore changed to mycophenolatmofetil (MMF) and an immune checkpoint blockade with the PD-1 inhibitor pembrolizumab was initiated in November 2016. Due to MMF-induced liver toxicity, MMF was switched to cyclosporine A (CsA) with normalized liver transaminases six weeks later. After six cycles of pembrolizumab the patient achieved a partial response. Follow up analysis sixty-five weeks later revealed a long-lasting tumor response with a partial remission of pancreatic and inguinal metastases and no flare of MG. Patients with a preexisting MG can be considered for treatment with immune checkpoint inhibitors if they have a life-threatening cancer and if other effective, long-lasting treatment options are not available. The risks and benefits of therapy should be weighed in a multidisciplinary setting and should be discussed thoroughly with the patient. Exacerbation of underlying MG can be potentially life-threatening and requires close monitoring in collaboration with neuromuscular specialists.

Sections du résumé

BACKGROUND
PD-1/PD-L1 inhibitors are promising approaches for advanced Merkel cell carcinoma (MCC). Nevertheless, these inhibitors bear a high risk for induction of immune-related adverse events (irAEs), particularly flares of preexisting autoimmune diseases. Neurological irAEs of PD-1/PD-L1 inhibitors are possibly underestimated and potentially fatal toxicities. Additionally, exacerbations of preexisting myasthenia gravis (MG) with a high MG-specific-related mortality have been reported.
CASE PRESENTATION
A 61-year-old woman with a history of MG since 2005 was treated with azathioprine and pyridostigmine after thymectomy. In March 2016, she was diagnosed with MCC. Six months later the tumor had progressed to stage IV and metastases were detected in lymph nodes and the pancreas. The immunosuppressive therapy was therefore changed to mycophenolatmofetil (MMF) and an immune checkpoint blockade with the PD-1 inhibitor pembrolizumab was initiated in November 2016. Due to MMF-induced liver toxicity, MMF was switched to cyclosporine A (CsA) with normalized liver transaminases six weeks later. After six cycles of pembrolizumab the patient achieved a partial response. Follow up analysis sixty-five weeks later revealed a long-lasting tumor response with a partial remission of pancreatic and inguinal metastases and no flare of MG.
CONCLUSIONS
Patients with a preexisting MG can be considered for treatment with immune checkpoint inhibitors if they have a life-threatening cancer and if other effective, long-lasting treatment options are not available. The risks and benefits of therapy should be weighed in a multidisciplinary setting and should be discussed thoroughly with the patient. Exacerbation of underlying MG can be potentially life-threatening and requires close monitoring in collaboration with neuromuscular specialists.

Identifiants

pubmed: 31142383
doi: 10.1186/s40425-019-0626-9
pii: 10.1186/s40425-019-0626-9
pmc: PMC6541996
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
Biomarkers, Tumor 0
CD274 protein, human 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

141

Références

Eur J Neurol. 2014 Mar;21(3):454-8
pubmed: 24330255
Lancet. 2017 Jun 24;389(10088):2492-2502
pubmed: 28434648
J Heart Lung Transplant. 2018 Jul;37(7):853-859
pubmed: 29680587
Nat Rev Dis Primers. 2017 Oct 26;3:17077
pubmed: 29072302
Eur J Cancer. 2017 Sep;82:128-136
pubmed: 28666240
Eur J Neurol. 2013 Jun;20(6):942-8
pubmed: 23448676
N Engl J Med. 2016 Jun 30;374(26):2542-52
pubmed: 27093365
Eur J Cancer. 2017 Apr;75:24-32
pubmed: 28214654
Nat Rev Cancer. 2012 Mar 22;12(4):252-64
pubmed: 22437870
J Neuromuscul Dis. 2017;4(2):169-173
pubmed: 28505981
Eur J Cancer. 2017 Mar;73:1-8
pubmed: 28064139
Front Oncol. 2018 Aug 29;8:310
pubmed: 30211111
Cancer Med. 2016 Sep;5(9):2294-301
pubmed: 27431483
Int J Dermatol. 2017 Apr;56(4):370-378
pubmed: 27868187
JAMA Oncol. 2016 Feb;2(2):234-40
pubmed: 26633184
J Clin Oncol. 2018 Oct 1;36(28):2872-2878
pubmed: 30125216
Eur J Cancer. 2016 Jun;60:210-25
pubmed: 27084345
Lancet Oncol. 2016 Oct;17(10):1374-1385
pubmed: 27592805
Ann Oncol. 2017 Feb 1;28(2):368-376
pubmed: 27687304
Curr Opin Neurol. 2017 Dec;30(6):659-668
pubmed: 28938341
Muscle Nerve. 2018 Apr;57(4):E120-E121
pubmed: 29193151

Auteurs

Anne Zaremba (A)

Department of Dermatology, University Hospital Essen, Essen, Germany. anne.zaremba@uk-essen.de.

Eleftheria Chorti (E)

Department of Dermatology, University Hospital Essen, Essen, Germany.

Finja Jockenhöfer (F)

Department of Dermatology, University Hospital Essen, Essen, Germany.

Saskia Bolz (S)

Department of Neurology, University Hospital Essen, Essen, Germany.

Selma Sirin (S)

Department of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, Essen, Germany.

Martin Glas (M)

Division of Clinical Neurooncology, Department of Neurology, University Hospital Essen, Essen, Germany.

Jürgen C Becker (JC)

Department of Dermatology, University Hospital Essen, Essen, Germany.
Translational Skin Cancer Research, German Cancer Consortium (DKTK), Partner Site Essen/Düsseldorf, Essen, Germany.

Selma Ugurel (S)

Department of Dermatology, University Hospital Essen, Essen, Germany.

Alexander Roesch (A)

Department of Dermatology, University Hospital Essen, Essen, Germany.

Dirk Schadendorf (D)

Department of Dermatology, University Hospital Essen, Essen, Germany.

Elisabeth Livingstone (E)

Department of Dermatology, University Hospital Essen, Essen, Germany.

Tim Hagenacker (T)

Department of Neurology, University Hospital Essen, Essen, Germany.

Lisa Zimmer (L)

Department of Dermatology, University Hospital Essen, Essen, Germany. lisa.zimmer@uk-essen.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH