001     140487
005     20240109101331.0
024 7 _ |a 10.1007/s00115-018-0571-8
|2 doi
024 7 _ |a pmid:30073487
|2 pmid
024 7 _ |a 0028-2804
|2 ISSN
024 7 _ |a 1433-0407
|2 ISSN
024 7 _ |a altmetric:46026894
|2 altmetric
037 _ _ |a DZNE-2020-06809
041 _ _ |a ger
082 _ _ |a 610
100 1 _ |a Knauss, S.
|b 0
245 _ _ |a [Neurological side effects of checkpoint inhibitors].
260 _ _ |a Heidelberg
|c 2019
|b Springer
264 _ 1 |3 online
|2 Crossref
|b Springer Science and Business Media LLC
|c 2018-08-02
264 _ 1 |3 print
|2 Crossref
|b Springer Science and Business Media LLC
|c 2019-02-01
336 7 _ |a article
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336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a In recent years the treatment of many tumor entities has been revolutionized by the use of modern immunotherapies with checkpoint inhibitors; however, good response rates are contrasted by many immune-mediated side effects. Neurological immune-mediated side effects are rare but often severe complications of checkpoint inhibitor treatment.A systematic search in the PubMed and Web of Sciences databases was carried out for case reports and studies on neurological side effects during checkpoint inhibitor treatment.A total of 42 articles on neurological side effects of checkpoint inhibitors with a total of 85 reported cases could be identified. The most frequently reported neurological side effects were myopathies, neuropathies, diseases of the neuromuscular endplates and encephalitides. Among those, encephalitides and myopathies with accompanying myocarditis were associated with the highest morbidity and mortality.Against the background of a rapidly increasing use of checkpoint inhibitors, this article provides an overview of currently available reports on the clinical courses of neurological side effects. Controlled studies on the treatment of neurological side effects are lacking. From case studies it can be assumed that early steroid treatment increases the probability of a complete remission of neurological symptoms. Typical symptom constellations must therefore be rapidly recognized and an immunosuppressive treatment must be initiated.
536 _ _ |a 344 - Clinical and Health Care Research (POF3-344)
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542 _ _ |i 2018-08-02
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650 _ 7 |a Antineoplastic Agents, Immunological
|2 NLM Chemicals
650 _ 2 |a Antineoplastic Agents, Immunological: adverse effects
|2 MeSH
650 _ 2 |a Antineoplastic Agents, Immunological: therapeutic use
|2 MeSH
650 _ 2 |a Drug-Related Side Effects and Adverse Reactions
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Immunotherapy
|2 MeSH
650 _ 2 |a Neoplasms: therapy
|2 MeSH
650 _ 2 |a Nervous System Diseases: chemically induced
|2 MeSH
700 1 _ |a Ginesta Roque, L.
|b 1
700 1 _ |a Hühnchen, P.
|b 2
700 1 _ |a Heinzerling, L.
|b 3
700 1 _ |a Böhmerle, W.
|0 P:(DE-HGF)0
|b 4
|e Corresponding author
700 1 _ |a Endres, M.
|0 P:(DE-2719)2811033
|b 5
|e Last author
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773 1 8 |a 10.1007/s00115-018-0571-8
|b : Springer Science and Business Media LLC, 2018-08-02
|n 2
|p 138-147
|3 journal-article
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|t Der Nervenarzt
|v 90
|y 2018
|x 0028-2804
773 _ _ |a 10.1007/s00115-018-0571-8
|g Vol. 90, no. 2, p. 138 - 147
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856 4 _ |u https://pub.dzne.de/record/140487/files/DZNE-2020-06809.pdf
856 4 _ |u https://pub.dzne.de/record/140487/files/DZNE-2020-06809.pdf?subformat=pdfa
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909 C O |p VDB
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
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913 1 _ |a DE-HGF
|b Gesundheit
|l Erkrankungen des Nervensystems
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914 1 _ |y 2019
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|t MDX-010 antibody, MDX-1379 melanoma vaccine, or MDX-010/MDX-1379 combination treatment for patients with unresectable or metastatic melanoma
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999 C 5 |y 2017
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|t Efficacy study of Ipilimumab versus placebo to prevent recurrence after complete resection of high risk stage III melanom
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999 C 5 |y 2017
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|t A study to compare BMS-936558 to the physician’s choice of either dacarbazine or carboplatin and paclitaxel in advanced melanoma patients that have progressed following anti-CTLA-4 therapy (checkmate 037)
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999 C 5 |y 2017
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|t Study of Nivolumab (BMS-936558) compared with dacarbazine in untreated, unresectable, or metastatic melanoma (checkmate 066)
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999 C 5 |y 2016
|2 Crossref
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999 C 5 |y 2017
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999 C 5 |y 2017
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|t A study of pembrolizumab (MK-3475) versus paclitaxel, docetaxel, or vinflunine for participants with advanced urothelial cancer (MK-3475-045/KEYNOTE-045)
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999 C 5 |y 2018
|2 Crossref
|t Nivolumab combined with Ipilimumab versus sunitinib in previously untreated advanced or metastatic renal cell carcinoma (checkmate 214)
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999 C 5 |y 2018
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|t Study of BMS-936558 (Nivolumab) compared to docetaxel in previously treated metastatic non-squamous NSCLC (checkmate057)
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999 C 5 |y 2018
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999 C 5 |y 2018
|2 Crossref
|t Phase 3 study of nivolumab or nivolumab plus Ipilimumab versus Ipilimumab alone in previously untreated advanced melanoma (checkmate 067)
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999 C 5 |y 2018
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|t An Immuno-therapy study to evaluate the effectiveness, safety and tolerability of nivolumab or nivolumab in combination with other agents in patients with advanced liver cancer (checkmate040)
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999 C 5 |y 2018
|2 Crossref
|t An investigational immuno-therapy study of nivolumab, and nivolumab in combination with other anti-cancer drugs, in colon cancer that has come back or has spread (checkmate142)
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999 C 5 |y 2018
|2 Crossref
|t A study of nivolumab in participants with metastatic or unresectable bladder cancer
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999 C 5 |y 2018
|2 Crossref
|t Study of nivolumab in patients with classical Hodgkin’s lymphoma (registrational) (checkmate 205)
|o ClinicalTrials.gov Study of nivolumab in patients with classical Hodgkin’s lymphoma (registrational) (checkmate 205) 2018
999 C 5 |y 2018
|2 Crossref
|t Efficacy study of nivolumab compared to Ipilimumab in prevention of recurrence of melanoma after complete resection of stage IIIb/c or stage IV melanoma (checkmate 238)
|o ClinicalTrials.gov Efficacy study of nivolumab compared to Ipilimumab in prevention of recurrence of melanoma after complete resection of stage IIIb/c or stage IV melanoma (checkmate 238) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of BMS-936558 (Nivolumab) compared to docetaxel in previously treated advanced or metastatic squamous cell non-small cell lung cancer (NSCLC) (checkmate 017)
|o ClinicalTrials.gov Study of BMS-936558 (Nivolumab) compared to docetaxel in previously treated advanced or metastatic squamous cell non-small cell lung cancer (NSCLC) (checkmate 017) 2018
999 C 5 |y 2018
|2 Crossref
|t Study to evaluate the safety and efficacy of two different dosing schedules of pembrolizumab (MK-3475) compared to Ipilimumab in participants with advanced melanoma (MK-3475-006/KEYNOTE-006)
|o ClinicalTrials.gov Study to evaluate the safety and efficacy of two different dosing schedules of pembrolizumab (MK-3475) compared to Ipilimumab in participants with advanced melanoma (MK-3475-006/KEYNOTE-006) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of Pembrolizumab (MK-3475) Compared to Platinum-Based Chemotherapies in Participants With Metastatic Non-Small Cell Lung Cancer (MK-3475-024/KEYNOTE-024)
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999 C 5 |y 2018
|2 Crossref
|t Study of pembrolizumab (MK-3475) in participants with advanced solid tumors (MK-3475-012/KEYNOTE-012)
|o ClinicalTrials.gov Study of pembrolizumab (MK-3475) in participants with advanced solid tumors (MK-3475-012/KEYNOTE-012) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of Pembrolizumab (MK-3475) in Participants With Advanced Solid Tumors (MK-3475-158/KEYNOTE-158)
|o ClinicalTrials.gov Study of Pembrolizumab (MK-3475) in Participants With Advanced Solid Tumors (MK-3475-158/KEYNOTE-158) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of pembrolizumab (MK-3475) in participants with advanced solid tumors (MK-3475-028/KEYNOTE-28)
|o ClinicalTrials.gov Study of pembrolizumab (MK-3475) in participants with advanced solid tumors (MK-3475-028/KEYNOTE-28) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of pembrolizumab (MK-3475) as monotherapy in participants with previously-treated locally advanced unresectable or metastatic colorectal cancer (MK-3475-164/KEYNOTE-164)
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999 C 5 |y 2018
|2 Crossref
|t Phase 2 study of MK-3475 in patients with microsatellite unstable (MSI) tumors
|o ClinicalTrials.gov Phase 2 study of MK-3475 in patients with microsatellite unstable (MSI) tumors 2018
999 C 5 |y 2018
|2 Crossref
|t Study of pembrolizumab (MK-3475) in participants with advanced urothelial cancer (MK-3475-052/KEYNOTE-52)
|o ClinicalTrials.gov Study of pembrolizumab (MK-3475) in participants with advanced urothelial cancer (MK-3475-052/KEYNOTE-52) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of pembrolizumab (MK-3475) in participants with relapsed or refractory classical Hodgkin lymphoma (MK-3475-087/KEYNOTE-087)
|o ClinicalTrials.gov Study of pembrolizumab (MK-3475) in participants with relapsed or refractory classical Hodgkin lymphoma (MK-3475-087/KEYNOTE-087) 2018
999 C 5 |y 2018
|2 Crossref
|t Study of two doses of pembrolizumab (MK-3475) versus docetaxel in previously treated participants with non-small cell lung cancer (MK-3475-010/KEYNOTE-010)
|o ClinicalTrials.gov Study of two doses of pembrolizumab (MK-3475) versus docetaxel in previously treated participants with non-small cell lung cancer (MK-3475-010/KEYNOTE-010) 2018
999 C 5 |y 2018
|2 Crossref
|t A study of atezolizumab compared with docetaxel in participants with locally advanced or metastatic non-small cell lung cancer who have failed platinum-containing therapy (OAK)
|o ClinicalTrials.gov A study of atezolizumab compared with docetaxel in participants with locally advanced or metastatic non-small cell lung cancer who have failed platinum-containing therapy (OAK) 2018
999 C 5 |y 2018
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|t A study of atezolizumab in participants with locally advanced or metastatic urothelial bladder cancer (cohort 1)
|o ClinicalTrials.gov A study of atezolizumab in participants with locally advanced or metastatic urothelial bladder cancer (cohort 1) 2018
999 C 5 |y 2018
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|t Avelumab in metastatic or locally advanced solid tumors (JAVELIN solid tumor)
|o ClinicalTrials.gov Avelumab in metastatic or locally advanced solid tumors (JAVELIN solid tumor) 2018
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999 C 5 |9 -- missing cx lookup --
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999 C 5 |9 -- missing cx lookup --
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999 C 5 |y 2011
|2 Crossref
|t YERVOY highlights of prescribing information
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|t BAVENCIO highlights of prescribing information
|o U.S. Food and Drug Administration BAVENCIO highlights of prescribing information 2017
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21