Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23284
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dc.contributor.authorLie, Gabrielle-
dc.contributor.authorWeickhardt, Andrew-
dc.contributor.authorKearney, Leighton G-
dc.contributor.authorLam, Que-
dc.contributor.authorJohn, Thomas-
dc.contributor.authorLiew, David F L-
dc.contributor.authorArulananda, Surein-
dc.date.accessioned2020-05-25T05:23:35Z-
dc.date.available2020-05-25T05:23:35Z-
dc.date.issued2020-04-
dc.identifier.citationTranslational Lung Cancer Research 2020; 9(2): 360-365en_US
dc.identifier.issn2218-6751-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/23284-
dc.description.abstractMalignant pleural mesothelioma (MPM) remains a deadly disease with limited therapeutic options beyond platinum/pemetrexed chemotherapy. Immune checkpoint inhibitors have demonstrated modest benefit in the second to later-line settings. An MPM patient from our institute developed myocarditis and myositis after 2 cycles of second-line nivolumab. Despite immunosuppression with corticosteroids and mycophenolate mofetil, there was ongoing rise in troponin levels which remained elevated for months. The patient developed an impressive but brief response following cessation of nivolumab. Myocarditis and myositis are rare complications of immune checkpoint inhibitors. Clinicians should be aware of these possible complications as myocarditis can result in mortality.en_US
dc.language.isoeng-
dc.subjectNivolumaben_US
dc.subjectcase reporten_US
dc.subjectmesotheliomaen_US
dc.subjectmyocarditisen_US
dc.subjectmyositisen_US
dc.titleNivolumab resulting in persistently elevated troponin levels despite clinical remission of myocarditis and myositis in a patient with malignant pleural mesothelioma: case report.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleTranslational Lung Cancer Researchen_US
dc.identifier.affiliationCardiologyen_US
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen_US
dc.identifier.affiliationMedical Oncologyen_US
dc.identifier.affiliationGeneral Medicineen_US
dc.identifier.affiliationPathologyen_US
dc.identifier.affiliationCancer Immuno-Biology Laboratory, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Heidelberg, Australiaen_US
dc.identifier.affiliationRheumatologyen_US
dc.identifier.doi10.21037/tlcr.2020.02.05en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-3399-5342en_US
dc.identifier.orcid0000-0002-5636-6381en_US
dc.identifier.orcid0000-0001-8451-8883en_US
dc.identifier.pubmedid32420076-
dc.type.austinCase Reports-
local.name.researcherJohn, Thomas
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptMedical Oncology-
crisitem.author.deptCardiology-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptRheumatology-
crisitem.author.deptClinical Pharmacology and Therapeutics-
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